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add to favorites ... nanjing Other Email:teresa@chembj.com Healthy Product 401900-40-1 Andarine Muscle Gain Steroid Powder S4
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Healthy Product 401900-40-1 Andarine Muscle Gain Steroid Powder S4 Email:teresa@chembj.com


Quick Detail:

Product Name S4
Synonyms S-3-(4-acetylamino-phenoxy)-2-hydroxy-2-methyl-N-(4-nitro-3-trifluoromethyl-phenyl)-propionamide;N-[4-Nitro-3-(trifluoromethyl)phenyl]-(2S)-3-[4-(acetylamino)phenoxy]-2-hydroxy-2-methylpropanamide;Ostarine;(2R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide;MK-2866;Andarine;Propanamide,3-[4-(acetylamino)phenoxy]-2-hydroxy-2-methyl-N-[4-nitro-3-(trifluoromethyl)phe nyl]-,(2S)-;sarM s4
CAS NO 401900-40-1
MF C19H18F3N3O6
MW 441.36
Purity >99%
Appearance Pale Yellow Solid
Melting point -15 ºC
mp  70-74ºC
Density  1.47
Storage temp Refrigerator
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Deliver time 4-6 working days via Air
Packing Galvanied iron barrel,net weight:200kg±0.05
Brand NJBN STEROID
Product Categories Pharmaceutical Intermediates;Heterocycles;Miscellaneous Reagents
Usage It is a potent and tissue-selective androgen receptor modulator (SARM)

Product Description:

Andarine, often known as S-4 or S4, is an androgen-like ingredient in the category of SARMs, with full name selective androgen receptor modulator. Andarine has been purchased by bodybuilders and gym rats during the last many years in an effort to put on their gains one stage further. Andarine is among the earliest SARMs and it is less potent both in anabolic and androgenic effects than other SARMs. Andarine was initially designed to treat conditions for example muscle wasting, brittle bones and benign prostatic hypertrophy, while using non-steroidal androgen antagonist bicalutamide as a lead compound. And today andarine can be used more often for lean muscle mass along with other bodybuilding benefits.Clearly, SARMs haven't made their way through the mainstream supplements industry in 2015, however with their incredible potential; we fully anticipate seeing them still increase in the ranks among the elite supplement groups for bodybuilders and sports athletes.
 
Application:

1.S-4 is designed for treating conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy, using the non-steroidal androgen antagonist bicalutamide as a lead compound.As an orally active partial agonist for androgen receptors, S-4 is effective in not only maintaining lean body mass but actually increasing it.

2.SARMS such as S4 can cause muscle growth in the same manner as steroids, however unlike testosterone and other anabolic steroids, SARMS (as nonsteroidal agents) do not produce the growth effect on prostate and other secondary sexual organs.The typical dose for cutting is 50 mg for a cycle of 6 to 8 weeks. The cycle should include using the product daily for 5 days and then taking 2 days off for the duration. Tasking the dose every day for the duration of the cycle can result in changes to vision.


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add to favorites ... nanjing Other Email:teresa@chembj.com Anabolic Steroids Hormone Solid 763113-22-0 Olaparib with Radiotherapy
Anabolic Steroids Hormone Solid 763113-22-0 Olaparib with radiotherapy Email:teresa@chembj.com


 Quick Detail:

Product Name Olaparib
Synonyms Olaparib;1-(Cyclopropylcarbonyl)-4-[5-[(3,4-dihydro-4-oxo-1-phthalazinyl)methyl]-2-fluorobenzoyl]piperazine;Olaparib(AZD-2281);Azd 2281;Azd2281;Azd-2281;Ku-0059436;4-[3-(4-Cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one Olaparib
CAS 763113-22-0
Purity 98%
MF C24H23FN4O3
MW 434.469
Appearance White Solid
Brand NJBN STEROID
Price Negotiated
Shipment EMS, FedEx, TNT, DHL, UPS
Delivery within 1 day after we get the payment
Product Categories APIs;API;Inhibitor;Inhibitors
Usage Olaparib is a potent poly(ADP-ribose) polymerase (PARP) inhibitor. Olaparib has been shown to induce significant killing of ATM-deficient lymphoid tumor cells in vitro and in vivo. Recent studies show that Olaparib increases radiosensitivity of a lung tumor xenograft, making it a potential candidate for use in combination with radiotherapy.
 
 Product Description:

1.Breast and ovarian cancer is a serious public health problem which is imposing severe threat on female. In recent years, the increasing rate of breast cancer incidence of China was even 1-2% higher than that of high- incidence countries. On the other hand, ovarian cancer still remains the most serious challenge for gynecologic oncologist because no mature approach for early stage diagnosis is available now. Upon diagnosis, about 70% cases are in advanced stage. Even subjecting to effective treatment and achieving complete alleviation, there are still 70% of patients who will get recurrence issue with 5-year survival rate hovering around 30-40%. Therefore, people are attempts to establish the three-level prevention and control measures of ovarian cancer like other chronic diseases. 
2.There is urgent need of a new medication for ovarian cancer treatment because platinum-based chemotherapy has limited drug duration before the occurrence of intolerable side effects. Olaparib, together with other PARP inhibitors under development are all oral preparations which can be better tolerated and can have more long-term applications compared with those drugs used in conventional chemotherapy. Olaparib can prevent an enzyme which participate in cellular repair, and is suitable for patients with certain genetic mutations. The drug also has good prospects in the treatment of other cancers, opening up considerable market opportunities for olaparib. 
3.In December 19, 2014, the FDA approved novel anti-cancer drug olaparib (Lynparza) for monotherapy to the patients of advanced ovarian cancer who has undergone at least 3 rounds of chemotherapy or patients of suspected BRCA mutations. At the same time, FDA approved the quantitation and classification of diagnostic kits for the detection of mutations in BRCA1 and BRCA2, BRACAnalysis CDx. Olaparib (Lynparza) is the first PARP inhibitor drugs which has been approved by FDA.In February 2, 2015, the European Union Food and Drug Administration (EMA) also approved olaparib to enter into market in the 28 countries of European Union including Iceland, Liechtenstein and Norway. But the indications of EMA and FDA approved are slightly different; the former is for the BRCA gene mutation cases, and also for the maintenance therapy for patients of advanced epithelial ovarian cancer who has previously received platinum-containing chemotherapy drugs and exhibit response and subject to recurrence.

Application:

1.Olaparib is a kind of novel poly ADP-ribose polymerase (PARP) inhibitors, including PARP1, PARP2, and PARP3. PARP mediates a DNA-repair mechanism which plays a important role in DNA damage repair and apoptosis, so olaparib specifically targets on the DNA repair mechanism of the targeting cell DNA repair and take effects by attacking the critical vulnerabilities of cancer cells carrying mutations in BRCA1 and BRCA2. Owing to this mechanism, it can be used for the maintenance therapy of patients of severe recurrent ovarian cancer who has breast cancer susceptibility gene (BRCA) mutation as well as being sensitive to platinum drug. 
Scientists from Harvard Medical School Dana - Farber Cancer Institute have found that the target site of olaparib is the polymerase Q (POLQ, also known POLθ). Those scientists found that a large number of patients of ovarian cancer has the genetic deficiency in the homologous recombination (homologous recombination, HR) repair pathway and dramatic up-regulated expression of POLQ greatly. Since HR is an important repair pathway for repairing broken DNA, they speculated that the major function of POLQ is to compensate for the lack of HR and participate in DNA repair.
2.The experiment has demonstrated that, in normal HR cells, knockout of POLQ would make HR activity increase significantly; while in HR deficient cells, the knockout of POLQ leads to cell death. POLQ contains RAD51 binding domain which can block the process of RAD51-mediated DNA repair. Related research has been published in the
February 12, 2015 Naturejournal with Raphael Ceccaldi being the first author of this research.Studies have revealed that about 10% of ovarian cancer patients and 5% of breast cancer patients contain BRCA1 or BRCA2 mutations. Both BRCA1 and BRCA2 belong to tumor suppressor genes as the major components of HR repair pathway. Their mutation suggests the loss of function for the HR repair pathway. In the cancer model of BRCA1 or BRCA2 mutations, blocking the important component for repairing single-strand DNA breaks --PARP can kill the mutated cancer cells. Put the BRCA-deficient mice with POLQ deficient mice for hybridization will cause the death of mouse embryos shortly after birth, which means that the coexistence of two repair pathway deficiency will cause embryonic lethality. 
3.These above findings suggest that olaparib, a kind of novel oral PARP inhibitor which is able to kill BRCA deficient cells, may be the effective drug for treating cancer patients who carry such mutations. Previously, researcher's knowledge of the BRCA mutation hasn't influenced patients' choice of treatment on either ovarian cancer or breast cancer. However, after the study, which means that olaparib can be used for the targeted therapy of cancer patients who carries BRCA1 or BRCA2 gene mutations with the therapeutic target site being the genetic deficiency of cancer cell genetic defect rather than a target organ.In ovarian and breast cancer cells, BRCA mutations are the first heavy blow to the survivability of cell because it increases their susceptibility to DNA damage. Through targeting the PARP-controlled adjuvant repair pathways, olaparib and its similar drugs achieve the second heavy blow to the survivability of cell. With the disorders of both of the two repairmen signaling pathways, the accumulation of DNA damage exert the third heavy blow to the cells.


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add to favorites ... nanjing Other Email:teresa@chembj.com Glucocorticoid Steroids Clobetasol Propionate 25122-46-7 Clobetasol Propionate for Skin Disorders
Glucocorticoid Steroids Clobetasol Propionate 25122-46-7 Clobetasol propionate for Skin Disorders Email:teresa@chembj.com


 Quick Detail:

Product Name Clobetasol propionate
Synonyms 17-propionate;cgp9555;clobesol;pregna-1,4-diene-3,20-dione,21-chloro-9-fluoro-11-beta,17-dihydroxy-16-beta-me;CLOBESTASOL PROPIONATE;CLOBETASOL-17-PROPIONATE;CLOBETASOLE PROPIONATE;CLOBETASOL PROPIONATE
CAS NO 25122-46-7
Einecs No 246-634-3
MF C25H32ClFO5
MW 466.97
Purity >99%
Packing Galvanied iron barrel,net weight:200kg±0.05
Storage temp -20°C Freezer
Chemical Properties White Crystalline Powder
Product Categories Pharmaceutical Intermediates;Heterocycles;Miscellaneous Reagents
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Uses For short-term topical treatment of the inflammatory and pruritic manifestations of moderate to severe corticosteroid-responsive dermatoses of the scalp.
Product Categories Organics;Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Pharmaceutical intermediate;TORADOL;Hormone Drugs

Product Description:

Clobetasol propionate /klobetsl/  is a corticosteroid of the glucocorticoid class used to treat various skin disorders including eczema and psoriasis. It is also highly effective for contact dermatitis caused by exposure to poison ivy/oak. Clobetasol belongs to US Class I (Europe: class IV) of the corticosteroids, making it one of the most potent available. It comes in shampoo, mousse, ointment and emollient cream presentations. It has very high potency and typically should not be used with occlusive dressings, or for extended continuous use (beyond two weeks). It is also used to treat several autoimmune diseases including alopecia areata, vitiligo, lichen sclerosus, and lichen planus.

 Application:

Clobetasol propionate is used for the treatment of various skin disorders including eczema, herpes labialis,psoriasis, and lichen sclerosus. It is also used to treat several auto-immune diseases including alopecia areata,vitiligo, lichen planus (auto immune skin nodules), and mycosis fungoides (T-cell skin lymphoma). It is used as first-line treatment for both acute and chronic GVHD of the skin.


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add to favorites ... nanjing Other Email:teresa@chembj.com Muscle Gain GMP Standard Polypeptide Hormones Carboprost Methylate Oxytocin
Muscle Gain GMP Standard Polypeptide Hormones Carboprost Methylate Oxytocin Email:teresa@chembj.com





Quick Details:



Product Name

Oxytocin

CAS No

60786-59-6

MF

C39H61N11O12S2

MW

940.1

Mol File

60786-59-6.mol

Assay

99%

Storage temp

−20°C

Molecular Structure



Shipping

EMS , FedEx , TNT , DHL , UPS

Delivery

Express Courier

Brand

NJBN STEROID

Appearance

White Crystalline Powder

Export Markets

Global

Sample

Free

Package

Discreet and safe packages according to different countries



Description:



1.Oxytocin is a powerful hormoneand acts as a neurotransmitter in the brain. When we hug or kiss a loved one, oxytocin levels increase. In fact, the hormone plays a huge role in pair bonding. Prairie voles, one of nature's most monogamous species, produce oxytocin in spades. This hormone is also greatly stimulated during sex, birth, and breastfeeding.

2.Oxytocin is a natural hormone that causes the uterus to contract.Oxytocin is used to induce labor or strengthen labor contractions during childbirth, and to control bleeding after childbirth. Oxytocin is also used to stimulate uterine contractions in a woman with an incomplete or threatened miscarriage.Oxytocin may also be used for purposes not listed in this medication guide.

3.Oxytocin is a hormone that also acts as a neurotransmitter in the brain. Some popular media have incorrectly labeled it the "love hormone," because it is associated with good feelings and emotions. But its role in the body is much more complex than that. It is not a bliss or hug hormone, but it does appear to be connected to human emotions and the regulation of childbirth and breast-feeding.In humans, oxytocin is thought to be released during hugging, touching, andorgasm in both genders. In the brain, oxytocin is involved in social recognition and bonding, and may be involved in the formation of trust between people and generosity.123 Oxytocin first became of interest to researchers when they discovered that breastfeeding women are calmer when exercising and experiencing stress than moms who were bottle-feeding. It is just one part of the important, complex neurochemical system in our bodies that helps us adapt to emotional situations.

4.What does oxytocin do in the body Greater amounts of oxytocin hormone levels appear to be associated with greater relaxation, more willingness to trust others, and general psychological stability. It appears to help us reduce our stress response and reduce general anxiety in people when produced.According to recent research, this hormone "is now believed to be involved in a wide variety of physiological and pathological functions such as sexual activity, penile erection, ejaculation, pregnancy, uterine contraction, milk ejection, maternal behavior, social bonding, stress and probably many more, which makes oxytocin and its receptor potential candidates as targets for drug therapy. From an innocuous agent as an aid in labor and delivery, oxytocin has come a long way in being touted as the latest party drug."Synthetic oxytocin is sold as medication under the trade names Pitocin and Syntocinon as well as generic oxytocin. It's not clear that synthetic oxytocin works in the same manner as the naturally occurring hormone.



 Application:



1.Oxytocin is a hormone used to help start or continue labor and to control bleeding after delivery. It is also sometimes used to help milk secretion in breast-feeding.In general, oxytocin should not be used to start labor unless there are specific medical reasons. Be sure you have discussed this with your doctor before receiving this medicine.This medicine is available only with your doctor's prescription.Novartis Pharmaceuticals removed Syntocinon® nasal spray from the market in March 1995.once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although this use is not included in product labeling, oxytocin is used in certain patients for the following:testing the ability of the placenta to support a pregnancy.

2.Oxytocin is a very abundant neuropeptide exerting a wide spectrum of central and peripheral effects as neurohormone, neurotransmitter, or neuromodulator. In the central nervous system, the oxytocin gene is predominantly expressed in magnocellular neurons in the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei. The magnocellular oxytocin neurons release their products into the general circulation in the neurohypophysis while the mediocellular oxytocin neurons secrete elsewhere in the CNS. Oxytocin is also produced in peripheral tissues, e.g., uterus, placenta, amnion, corpus luteum, testis, and heart. Oxytocin is a potent stimulator of spontaneous erections in rats and is involved in ejaculation. The typical actions of peripheral oxytocin are stimulation of uterine smooth muscle contraction during labor and milk ejection during lactation. Oxytocin receptors have also been identified in other tissues, including the kidney, heart, thymus, pancreas, and adipocytes.


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add to favorites ... nanjing Other Email:teresa@chembj.com Pituitary Muscle Gain Growth Powders 434-05-9 Primobolan Methenolone Acetate
Pituitary Muscle Gain Growth Powders 434-05-9 Primobolan Methenolone Acetate Email:teresa@chembj.com


Quick Detail: 

Product Name:Methenolone Acetate
Alias: primobolone;1(5a)-androsten-1beta-methyl-17beta-ol-3-one Acetate
CAS No.: 434-05-9
EINECS No: 207-097-0
Grade : Pharmaceutical Grade
Storage: Shading, confined preservation
Brand Name:NJBNSTEROID
Lead time:within 24 hours upon receipt of payment
Delivery time:4-6 working days
Delivery: EMS, DHL, TNT, FedEx, UPS
Usage :pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.methenolone can be suppressive of the hypothalamic-pituitary-gonadal axis.
 
Application:
 
1.The typical "safe" dosage for men is 100-200mg per week, a level that should produce at least some noticeable muscle growth. In European medicine it is not uncommon for Primobolan to be used safely at such a dosage for extended periods of time.

2.Among athletes, men may respond to weekly doses of 200mg but regular users will often inject much higher doses looking for a stronger anabolic effect. It is not uncommon for a bodybuilder to take as much as 600 or 800mg per week, a range which appears to be actually quite productive. Of course androgenic side effects may become more pronounced with such an amount, but in most instances it should still be quite tolerable.

3.Women respond well to a dosage of 50-100mg per week, although (as stated above) the oral should usually be given preference. Additionally, some choose to include Winstrol Depot or Oxandrolone and receive a greatly enhanced anabolic effect.


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add to favorites ... nanjing Other Email:teresa@chembj.com Fitness Prostate Cancer Anabolic Peptide 33515-09-2 Gonadorelin for Keeping Energy
Fitness Prostate Cancer Anabolic Peptide 33515-09-2 Gonadorelin for Keeping Energy Email:teresa@chembj.com
 

 Quick Detail:

Product Name Gonadorelin
Synonyms LUTEINIZING HORMONE-RELEASING HORMONE (SEA BREAM);LUTENIZING HORMONE RELEASING HORMONE HUMAN;LUTEINIZING HORMONE-RELEASING HORMONE (LAMPREY III);LUTEINIZING HORMONE-RELEASING HORMONE (LH-RH), HUMAN;LUTEINIZING HORMONE RELEASING HORMONE HUMAN;LUTEINIZING HORMONE RELEASING HORMONE (HUMAN) PORCINE, RAT;LUTEINIZING HORMONE-RELEASING FACTOR (LAMPREY III);LUTEINIZING HORMONE-RELEASING HORMONEACETATE
CAS NO 33515-09-2
EINECS 232-895-0
MF C55H75N17O13
MW 1182.29
Purity >99%
Mol File 33515-09-2.mol
density  1.54
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Deliver time Within 24 hours after receiving the payment
Brand Name NJBN STEROID
Product Categories Gonadotropin-releasing hormone (GnRH);Peptide Receptors;peptide
Usage Benzyl alcohol is used as a bacteriostatic preservative at low concentration in intravenous medications, cosmetics and topical drugs.The use of benzyl alcohol as a 5% solution has been approved by the U.S. FDA in the treatment of head lice in children older than 6 months and in adults
 
Product Description:
 
1.Gonadorelin is a medicine that is the same as gonadotropin-releasing hormone (GnRH) that is naturally released from the hypothalamus gland. GnRH causes the pituitary gland to release other hormones (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]). LH and FSH control development in children and fertility in adults.
2.Gonadorelin is a man-made protein that is like a hormone in the body called gonadotropin-releasing hormone (GnRH). GnRH causes the pituitary gland to release other hormones including luteinizing hormone (LH) and follicle-stimulating hormone (FSH). LH and FSH are important for proper development in children and fertility in adults.Gonadorelin is used to test how well the hypothalamus and pituitary glands are working.Gonadorelin may also be used for purposes other than those listed in this medication guide.
 
Application:
 
1.Gonadorelin is used to test how well the hypothalamus and the pituitary glands are working. It is also used to cause ovulation (release of an egg from the ovary) in women who do not have regular ovulation and menstrual periods because the hypothalamus gland does not release enough GnRH.
2.Gonadorelin is a gonadotropin-releasing hormone. It works by causing the pituitary gland to release other hormones (luteinizing hormone and follicle-stimulating hormone) that control development in children and fertility in adults.
Checking whether the pituitary gland is producing LH and FSH in the correct levels. This can help in the diagnosis of various hormonal disorders, including infertility and delayed puberty.
 

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add to favorites ... nanjing Other Email:teresa@chembj.com Anabolic-Pure Pharmaceutical Raw Materials CAS 137862-53-4 Valsartan for Antihypertensive
Anabolic-pure Pharmaceutical Raw Materials CAS 137862-53-4 Valsartan for Antihypertensive Email:teresa@chembj.com


Quick Detail:

Product Name Valsartan 
Alias N-(1-OXOPENTYL)-N-[[2'-(1H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-L-VALINE;VALSARTAN;CGP-48933;DIOVAN;3-methyl-2-[pentanoyl-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methyl]amino]-butanoicacid;VALSARTAN,MMSTANDARD;USPSTANDARD;VALSARTAN, RELATED COMPOUND A(R)-N-VALERYL-N-([2'-(1-H-TETRAZOLE)-5-YL)-BIPHENYL-4-YL]-METHYL)-VALINE USP STANDARD
CAS NO 137862-53-4
MF C24H29N5O3
MW 435.52
Purity >99%
Appearance White Crystalline Powder
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Packing Galvanied iron barrel,net weight:200kg±0.05
Brand NJBN STEROID
Product Categories Active Pharmaceutical Ingredients;Antihypertensive;APIs;Intermediates & Fine Chemicals;Pharmaceuticals;API's;Aromatics;Chiral Reagents;Heterocycles;API Reference Standard Free Base API;DIOVAN;Inhibitors
Usage A nonpeptide angiotensin II AT1-receptor antagonist. Antihypertensive.

Product Description:

1.Valsartan (trade name Diovan) is an angiotensin II receptor antagonist (commonly called an ARB, or angiotensin receptor blocker), that is selective for the type I (AT1) angiotensin receptor. Valsartan is mainly used for treatment of high blood pressure, congestive heart failure, and to increase the chances of living longer after a heart attack.

2.Valsartan is used alone or in combination with other medications to treat high blood pressure. It is also used to treat heart failure (condition in which the heart is unable to pump enough blood to the rest of the body) and to improve survival after a heart attack. Valsartan is in a class of medications called angiotensin II receptor antagonists. It works by blocking the action of certain natural substances that tighten the blood vessels, allowing the blood to flow more smoothly and the heart to pump more efficiently.

3.High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Application:

1.Valsartan is an angiotensin II receptor antagonist. Valsartan keeps blood vessels from narrowing, which lowers blood pressure and improves blood flow.Valsartan is used to treat high blood pressure (hypertension) in adults and children who are at least 6 years old. Valsartan is also used in adults to treat heart failure, and to lower the risk of death after a heart attack.Valsartan is sometimes given together with other blood pressure medications.
Valsartan may also be used for purposes not listed in this medication guide.

2.Valsartan is used to treat high blood pressure and heart failure. It is also used to improve the chance of living longer after a heart attack. In people with heart failure, it may also lower the chance of having to go to the hospital for heart failure. Valsartan belongs to a class of drugs called angiotensin receptor blockers (ARBs). It works by relaxing blood vessels so that blood can flow more easily. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems.

3.Valsartan is used to treat high blood pressure, congestive heart failure, and to reduce death for people with left ventricular dysfunction after having had a heart attack.There is contradictory evidence with regard to treating people with heart failure with a combination of an angiotensin receptor blocker like valsartan and an angiotensin-converting enzyme inhibitor, with two major clinical trials (CHARM-additive and ValHeFt) showing a reduction in death, and two others (VALIANT and ONTARGET) showing no benefits, and more adverse effects including heart attacks.In people with type II diabetes and high blood pressure or albumin in the urine, valsartan is used to slow the worsening and the development end-stage renal disease.


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add to favorites ... nanjing Other Email:teresa@chembj.com CAS 656247-17-5 Potent Inhibitor Intedanib (Vargatef)
CAS 656247-17-5 Potent inhibitor Intedanib(Vargatef) Email:teresa@chembj.com


 Quick Detail:

Product name Intedanib
Synonyms Intedanib;Vargatef;Nintedanib;Nintedanib (BIBF 1120);Nintedanib/Intedanib/Vargatef;Intedanib Vargatef;methyl (3Z)-3-[[4-[methyl-[2-(4-methylpiperazin-1-yl)acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1H-indole-6-carboxylate Nintedanib (BIBF 1120);Vargatef (nintedanib)
CAS register number 656247-17-5
Molecular formula C31H33N5O4
MW 539.62482
Mol File 656247-17-5.mol
Assay 99%
Appearance White crystalline powder
Package 1kg/aluminium foil bag or as required
Minimum order quantity 10g
Shipping By express courier
Shipping leading time Within 24 hours after receiving the payment
Payment options Western Union , MoneyGram , T/T ,  Bitcoin
Price Negotiated 
Product Categories Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitors
Usage It is an indolinone derivative potently blocking VEGF-, PDGF-, and FGF-receptor kinases; an indolinone as triple angiokinase inhibitors.

Product Description:

1.Nintedanib, marketed under the brand names Ofev and Vargatef, is a medication used for the treatment of idiopathic pulmonary fibrosis (IPF) and along with other medications for some types of non-small-cell lung cancer.Common side effects include abdominal pain, vomiting, and diarrhea. It is a small molecule tyrosine-kinase inhibitor, targeting vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR) and platelet derived growth factor receptor (PDGFR).It was developed by Boehringer Ingelheim. At an assumed cost of 39,300 pounds per year it does not appear to be cost effective for IPF in the United Kingdom.
2.Nintedanib is also called by its brand name Vargatef. It is a treatment for a type of non small cell lung cancer called adenocarcinoma.Nintedanib is for people who have already had one type of chemotherapy and whose cancer has grown back or has spread. You have it with a type of chemotherapy called docetaxel.You usually keep taking it for as long as it is working unless side effects get too bad.You may have nintedanib as part of clinical trials for other types of cancer.


 Applications:

Nintedanib is a cancer growth blocker. It works by blocking particular proteins called protein kinases in cancer cells. The protein kinases encourage the cancer to grow. Nintedanib blocks a number of these proteins and is called a multi kinase inhibitor. It also stops the cancer cells growing their own blood vessels, which the cells need to be able to grow.Nintedanib may shrink the cancer or stop it growing for a time.


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add to favorites ... nanjing Other Email:teresa@chembj.com 57773-63-4 Petides 2mg/Vial Gnrh Triptorelin Acetate for Advanced Prostate Cancer
57773-63-4 Petides 2mg/Vial Gnrh Triptorelin Acetate for Advanced Prostate Cancer Email:teresa@chembj.com




  Quick Detail:



Product Name

Triptorelin

Product Categories

Amino Acid Derivatives;Peptide

CAS No

57773-63-4

Mol File

57773-63-4.mol

Assay

99%

MF

C64H82N18O13

MW

1311.45

Molecular Structure



Appearance

White or off-white crystalline powder

Packing

1kg/aluminium foil bag or as required

Minimum order quantity

40g

Drug Class

Injectable steroid,oral steroid, bodybuilding steroid

Delivery time

Within 24 hours upon receipt of payment

Shipping

EMS , DHL , TNT , FedEx , UPS

Brand

NJBN STEROID

Categories

Pharmaceutical; Active Pharmaceutical Ingredients; Biochemistry; Steroids

Usage

promoting ovulation



 Product Description:



1.The active ingredient of triptorelin is a synthetic gonadotropin-releasing hormone (GnRH) analogue, which is also known as decapeptyl, diphereline, triptorelin acetate, gonadorelin. It is an antineoplastic drug, whose pharmacological effects are same with goserelin, buserelin, and its structure is modified by natural molecular structure of the sixth L-glycine that is replaced by D-tryptophan to promote efficiency and prolong the plasmic half-life time, as well as enhance drug efficacy. After intramuscular injection, it initially stimulates the pituitary gland to release luteinizing growth hormone (LH) and follicle-stimulating hormone (FSH). When the pituitary over a long period of stimulation will be into the refractory period, that reduced the release of gonadotropin, leading to sex hormones reduction to castrate levels. These effects are reversible. Subcutaneous administration is rapidly absorbed, and Tmax is 15min, and the effect is maximum at 1h. The intramuscular injection of sustained release formulations can maintain the efficacy reaching 28d or more.

2.Triptorelin, a decapeptide (pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-Pro-Gly-NH2), is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer orbreast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and inassisted reproduction. It is also used as therapy in cases of gender dysphoria. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals). In the United States, it is sold by Watson Pharmaceuticals as Trelstar. In Iran Triptorelin is marketed under the brand name Variopeptyl (Varian Darou Pajooh).During the treatment of prostate cancer it does cause a surge of testosterone (an initial uplevel of testosterone levels), known as a flare effect. In men a reduction of serum testosterone levels into the range normally seen after surgical castration occurs approximately two to four weeks after initiation of therapy. In contrast, gonadotropin-releasing hormone antagonists do not cause a surge, but a sudden reduction of testosterone levels.

3.Triptorelin - GnRH (Gonadotropin-releasing hormone) is being used during PCT (Post Cycle Therapy) for users recovery or restart their normal testosterone production. GnRH has been used for a long time by horse breeders as a way to stimulate the anterior pituitary to release follicle-stimulating hormone (FSH). With this stimulation, the horses became more fertile, and breeding would commence.FSH is one of the two main hormones responsible for sexual reproduction regulations (along with LH). FSH plays the main role in stimulating the production and maturation of germ cells (which either become sperm in males, or eggs in females). This mean, when your pituitary is stimulated to produce FSH (as a reaction from GnRH), FSH will begin to stimulate the production of sperm in men. GnRH pulses in our bodies, and that pulse controls when we produce FSH.

4.GnRH is a chemical that is sent from our brain to the pituitary to tell it to produce both FSH and LH. When a small pulse dose of GnRH is injected, your pituitary receives that signal to start producing. This will result in both an increase in testosterone serum (as a result from the LH stimulation) and an increase in sperm (or egg in a female case) count. The result may be an effective jumpstart to our reproductive system for steroid users.



Applications:



Triptorelin is a type of hormone therapy drug called a gonadotropin releasing hormone blocker. It lowers the level of testosterone in men and oestrogen in women. It does this by stopping the release of luteinising hormone from the pituitary gland. In men, this stops the testicles producing the male sex hormone, testosterone. In women, it stops the ovaries from producing oestrogen.Prostate cancer depends on testosterone, to grow. Hormone therapies that lower the level of testosterone can slow down the growth of cancer or shrink it.Some breast cancers depend on oestrogen to grow. Lowering the level of oestrogen can slow or stop the growth of the cancer.


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add to favorites ... nanjing Other Email:teresa@chembj.com Factory Natural Oral Raw Powders 434-07-1 Anadrol for Muscle Building
Factory Natural Oral Raw Powders 434-07-1 Anadrol for Muscle Building Email:teresa@chembj.com


Quick Detail: 

Product Name:Anadrol
CAS No.: 434-07-1
EINECS No: 207-098-6  
Grade : Pharmaceutical Grade
Storage: Shading, confined preservation
Brand Name:NJBN STEROID
Lead time:within 24 hours upon receipt of payment
Delivery time:Within 24 hours after receiving the payment
Delivery: EMS, DHL, TNT, FedEx, UPS
 
Application:
 
1.Anadrol is most likely second only to Dianabol (methandrostenolone) as a bodybuilding anabolic steroid. Additionally, it has had considerable medical importance particularly for treatment of anemia, and more recently to help maintain lean body mass in HIV-compromised patients.

2.Presented most commonly as a 50 mg tablet, Anadrol is one of the strongest androgenic steroids available. Despite very low binding affinity with the androgen receptor, Anadrol is highly effective in
promoting extensive gains in body mass, mostly by greatly improving protein synthesis. For this reason, it is often used by bodybuilders and athletes.


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add to favorites ... nanjing Other Email:teresa@chembj.com Local Anesthetics Steroid White Crystalline Powder 23239-88-5 Benzocaine Hydrochloride
Local anesthetics Steroid White Crystalline Powder 23239-88-5 Benzocaine hydrochloride Email:teresa@chembj.com


Quick Detail:
 
1.Product Name:Benzocaine hydrochloride
2.Synonyms:ETHYL 4-AMINOBENZOATE HYDROCHLORIDE;BENZOCAINE HCL;BENZOCAINE HYDROCHLORIDE;Benzocaine hydrochl;Benzoic acid, 4-aMino-,ethyl ester, hydrochloride (1:1)
3.CAS NO: 23239-88-5
4.Assay: 99%
5.Appearance: White crystalline powder
6.Packing: foil bag or tin or customerized
8.MF: C9H11NO2.ClH
9.MW: 201.65
10.Mol File : 23239-88-5.mol
11.Brand:NJBN STEROID
12.Delivery time :Within 24 hours upon receipt of payment
13.Shipment : EMS, DHL, TNT, FedEx, UPS
14.Usage : used for application direct to the skin.
  
Product Description:
 
1.The potential of benzocaine-hydrochloride as an aid in the transport of fish was investigated. When used at a concentration of 25 mg/l the anaesthetic caused a reduction in the excretion of ammonia and carbon dioxide by the fish, while, as a result of the reduced activities of the fish, the pH and alkalinity values of the transport water remained fairly constant. When benzocaine-hydrochloride was not used, the activities of the fish produced a significant deterioration in water quality evidenced by the accumulation of ammonia and carbon dioxide.
2.Benzocaine hydrochloride salt is the hydrochloride salt form of the local anesthetic benzocaine, the pharmacological effects with benzocaine, procaine weaker than the effect of anesthesia. Partially absorbed slowly, lasting effect. Because they do not dissolve in water, can not be used for anesthesia, pain relief, anti-itch effect, drugs are usually made of powdered or oil paste, used to treat wounds Clinically, ulcers, burns, skin abrasions and hemorrhoids.
Benzocaine is also called amino benzoate, Xinaixixin.
 
Applications:
 
1.Benzocaine is an anaesthetic drug, mostly used for application direct to the skin. Benzocaine HCl is a salt modification of benzocaine, formed when benzocaine is complexed with hydrochloric acid. Often, drug salts have enhanced properties compared with the parent compound. For example, benzocaine hydrochloride is more water soluble than benzocaine, making it more appropriate for oral administration.
2.There are quite a few different uses for Benzocaine, these include:
(1)As an ingredient in cough syrups
(2)To treat cold sores
(3)To treat toothache
(4)To treat irritation from dentures
(5)To treat earache
(6)As a surgical local anesthetic
(7)In condoms used to delay ejaculation
(8)To tranquilize Fish
3.Benzocaine is the main local anesthesia for pain experienced in the gums, teeth and also for relieving sore throat. Apart from treating oral irritations it is also used to treat otic pain i.e. pain experienced in the ear. Moreover it is incorporated in certain surgical procedures as a local anesthesia. It comes prepared in a variety of ways such as gel, aerosol and paste for otic purposes. Benzocaine spray used to relieve pain in the throat and lining of the mouth is not applicable to children under the age of two unless prescribed by a doctor. The spray is used on patients fitting dentures on their gums to relieve pain. It is important to note that in such cases the spray should not be a long term solution to pain caused by poorly fitted dentures. 


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add to favorites ... nanjing Other Email:teresa@chembj.com CAS 434-05-9 Methenolone Acetate Raw Material Steroid for Muscle Gain
CAS 434-05-9 Methenolone Acetate  Raw Material Steroid for Muscle Gain Email:teresa@chembj.com


Quick Detail:

Product Name:Methenolone Acetate
Synonyms: primobolone;1(5a)-androsten-1beta-methyl-17beta-ol-3-one Acetate
CAS Registry Number:434-05-9
EINECS: 207-097-0
Assay: 99% min.
Grade : Pharmaceutical Grade
Molecular Formula: C22H32O3
Molecular Weight: 344.4877
Character: White crystalline powder.
Delivery time :within 24 hours upon receipt of payment
Delivery: EMS, DHL, TNT, FedEx, UPS
Keywords : bodybuilding , steroid hormone , raw material powder  
Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

 Specification:

COA:

Test Standard Results
Description White Or Almost White Crystalline Powder White Crystalline Powder
Melting Point 139ºC~ 145ºC 139.5ºC~ 142.5ºC
Loss On Drying ≤0.50% 0.32%
Specific Rotation +55°~ +58° +57.2°
Assay 97~102% 98.55%
Conclusion The specification conform with Enterprise Standard.
 
HPLC:



Product Description:

1.Methenolone Acetate is void of the typical C17-alpha alkylation common in nearly all oral anabolic steroids, and therefore Primobolan presents no measurable hepatotoxic effects on the body. Oral Primobolan has failed to demonstrate any changes in liver enzyme values that would be cause for concern. Primobolan in particular does possess in its own right a resistance to hepatic metabolism and breakdown, and only one incidence of a death resultant of hepatotoxicity and liver failure from oral Primobolan has been recorded in one male elderly individual who was prescribed the compound for the purpose of treating anemia. Methenolone Acetate is the injectable version of the steroid methenolone powders. It is the same compound as the one in Primobolan Orals (methenolone acetate), both produced by Schering. In this injectable version, an enanthate ester is added to the steroid, which makes for a slow and gradual release from the site of injection. Its length of activity would thus be quite similar to Testosterone enanthate, with blood levels remaining elevated for approximately two weeks.

2.Methenolone Acetate  is a brand name for the anabolic steroid methenolone acetate. This agent is very similar in action to Primobolan® Depot, except here the drug is designed for oral administration instead of injection. Methenolone acetate is a non-c17-alpha-alkylated oral steroid, one of only a few commercially available oral agents that presents limited liver toxicity to the user. It is also highly favored for its properties as a moderately effective anabolic with low androgenic and no estrogenic properties. It is, likewise, commonly used during cutting phases of training, when lean tissue growth and solid muscularity, not raw bulk, are the key objectives.

 Applications:

1.Methenolone Acetate is the injectable version of the steroid methenolone powders.The effective dose of Primobolan (Methenolone Acetate) in the type of injection is 200-300 mg weekly. In case you want to take this drug by mouth, 50-150 mg in a day is the directed measure. For men, 50-100 mgs /day is the accurate as well actual measure by mouth, while for women, 10-25 mgs /day is the finest quantity. If you have to administrate them as injections, the top dose for Primobolan (Methenolone Acetate) injection is 350-600 mg/week for men. Women have to use 100 mg weekly of this medication. Primobolan (Methenolone Acetate) injectable active life is near ten-fortheen days, while the dynamic life of this medicine in the form of pills is approximate 4-6 hours. The time of its finding is four-five weeks
2.It is the same compound as the one in Primobolan Orals (methenolone acetate), both produced by Schering. In this injectable version, an enanthate ester is added to the steroid, which makes for a slow and gradual release from the site of injection. Its length of activity would thus be quite similar to Testosterone enanthate, with blood levels remaining elevated for approximately two weeks. Methenolone itself is a long acting anabolic, with extremely low androgenic properties.
3.It's anabolic effect is also quite mild, its potency is considered to be slightly less than Deca Durabolin (nandrolone decanoate) on a milligram for milligram basis. For this reason, Primobolan is most commonly used during cutting cycles when a mass increase is not the main goal. Some athletes do prefer to combine a mild anabolic like "Primo" with bulking drugs such as Dianabol, Anadrol, or testosterone however, presumably to lower the overall androgen dosage and minimize uncomfortable side effects. When choosing between Primobolan versions, the injectable is preferred over the oral, as it is much more cost effective.
4.Primobolan (Methenolone Acetate) is void of the typical C17-alpha alkylation common in nearly all oral anabolic steroids, and therefore Primobolan presents no measurable hepatotoxic effects on the body. Oral Primobolan has failed to demonstrate any changes in liver enzyme values that would be cause for concern. Primobolan in particular does possess in its own right a resistance to hepatic metabolism and breakdown, and only one incidence of a death resultant of hepatotoxicity and liver failure from oral Primobolan has been recorded in one male elderly individual who was prescribed the compound for the purpose of treating anemia. Therefore, higher doses of oral Primobolan can indeed be utilized but it must be noted that oral Primobolan does still possess a measure of resistance to metabolism and breakdown in the liver, and therefore the risk of hepatotoxicity from Primobolan must not be completely ignored, especially as doses of the oral format are increased to higher and higher amounts.


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add to favorites ... nanjing Other Email:teresa@chembj.com Factory Anabolic Pharmaceutical Ingredient Glucurolactone 32499-92-6 for Ascorbic Acid Synthesis
Factory Anabolic Pharmaceutical Ingredient Glucurolactone  CAS 32499-92-6  for Ascorbic Acid Synthesis Email:teresa@chembj.com


Quick Detail:

Product Name Glucuronolactone
CAS NO 32499-92-6
Einecs No 202-509-5
MF C6H8O6
MW 176.12
Purity >99%
Packing Galvanied iron barrel,net weight:200kg±0.05
Product Categories Pharmaceutical Intermediates;Heterocycles;Miscellaneous Reagents
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Uses Use glucuronolactone as a precursor for ascorbic acid synthesis.According to The Merck Index, it is also used as adetoxicant.
 
 Product Description:

1.Glucuronolactone, also known as D-Glucuronolactone, DGL and D-Glucoronic Acid, is an organic metabolite found in the body. A metabolite is a substance that results from the metabolism of glucose in the human liver. This water-soluble crystalline compound has been made a common component in stimulants and energy drinks like Red Bull owing to research which revealed that DGL can boost energy, lessen sleepiness and increase alertness and reaction time. 

2.The human liver naturally produces glucuronolactone from glucose and controls glycogen formation. With glucuronic acid as its immediate precursor, it is used for the oral administration of the said acid in the treatment of collagen and joint diseases. It is one of the basic units of and an element of Chondroitin Sulfate and is considered by some experts to be beneficial in making joint, tendon and ligament healthy and elastic. It has also been used in medicine as an antiarthritic agent it being a vital structural component of almost all fibrous and connective tissues in animals.

3.DGL also has a direct participation in detoxifying the liver through glucuronidation. The body carries this substance which hastens and stimulates the removal of the harmful substances endogenic and exogenic noxal. Glucuronidation aids in the elimination of medicines from the body. In the process, the medicines typically consumeglucuronolactone faster than the body can naturally produce it, and so diminishing the concentrations of other substances like glycogen. Hence, DGL has been incorporated to some medicines to increase their tolerance level and improve their elimination.
 
 Application:

1.Glucuronolactone is metabolized to glucaric acid, xylitol, and L-xylulose, and humans may also be able to use glucuronolactone as a precursor for ascorbic acid synthesis.According to The Merck Index, it is also used as adetoxicant.The liver uses glucose to create glucuronolactone, which inhibits the enzyme B-glucuronidase (metabolizesglucuronides), which should cause blood-glucuronide levels to rise

2.Theoretically, higher blood-glucuronides should help remove toxins from the body, leading to the claim that energy drinks are detoxifying.Free glucuronic acid (or its self-ester glucuronolactone) has less effect on detoxification than glucose, because the body synthesizes UDP-glucuronic acid from glucose. Therefore, sufficient carbohydrate intake provides enough UDP-glucuronic acid for detoxication, and foods rich in glucose are usually abundant in developed nations.

3.Glucuronolactone is a popular ingredient in energy drinks with claims that it detoxifies the body. Although levels of glucuronolactone in energy drinks can far exceed those found in the rest of the diet, the European Food Safety Authority (EFSA) has concluded that exposure to glucuronolactone from regular consumption of energy drinks is not a safety concern. The no-observed-adverse-effect level of glucuronolactone is 1000 mg/kg/day.


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add to favorites ... nanjing Other Email:teresa@chembj.com High Quality CAS 557795-19-4 Sunitinib Malate/Sunitinib Treatment of Advanced Renal Cell Cancer
High Quality CAS 557795-19-4 Sunitinib Malate/Sunitinib Treatment of Advanced Renal Cell Cancer Email:teresa@chembj.com


Quick Detail:

Product Name Sunitinib
Synonyms sunitinib;SUNITINIB-D4;SUNITINIB MALEATE;n-(2-(diethylamino)ethyl)-5-((z)-(5-fluoro-1,2-dihydro-2-oxo-3h-indol-3-ylidene)methyl)-2,4-dimethyl-1h-pyrrole-3-carboxamide;SUNITINIB BASE;1H-Pyrrole-3-carboxamide, N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-;SUNITINIBMALEATE(FORR&DONLY);N-(2-diethylaminoethyl)-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)meth yl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
CAS NO 557795-19-4
MF C26H31FN4O6
MW 514.55
Purity >99%
Appearance Yellow Solid
Packing Galvanied iron barrel,net weight:200kg±0.05
Storage temp 2-8° C
mp  189-191°C
Product Categories Active Pharmaceutical Ingredients;Sunitinib;Molecular Targeted Antineoplastic;Heterocyclic Compounds;anti-neoplastic;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Tyrosine Kinase Inhibitors;Pharmaceutical intermediate;API;Isotope Labelled Compounds;SU-11248;Inhibitors
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Uses A multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Antineoplastic

Product Description:

Sunitinib is a cancer medicine that interferes with the growth and spread of cancer cells in the body. Sunitinib is used to treat certain types of advanced or progressive tumors of the digestive system, the pancreas, or the kidneys.Sunitinib may also be used for purposes not listed in this medication guide.


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add to favorites ... nanjing Other Email:teresa@chembj.com 2446-23-3 Anabolic Steroids 4-Chlorodehydromethyl Turinabol for Male Sexual Dysfunction Treatment
2446-23-3 Anabolic Steroids 4-Chlorodehydromethyl Turinabol For Male Sexual Dysfunction Treatment
Email:teresa@chembj.com


Quick Detail:
 
Product Name:Turinabol
Synonyms: 4-Chlorodehydromethyltestosterone
CAS NO.: 2446-23-3
EINECS: 200-551-9
Assay: 98%
Grade: Pharmaceutical Grade
Storage: Shading, confined preservation (usually packaging by foil bag or tin )
MOQ:10g
Delivery time: Within 6 days upon receipt of payment
Delivery: EMS, DHL, TNT, FedEx, UPS
Usage: pharmaceutical material, Steroid hormone, Anabolin. For the treatment of male hypogonadism and reduced sperm infertility.
 
Product Description:
 
1.Turinabol was the first original product of Jenapharm, an East German pharmaceutical company. The patent registration took place in 1961. The idea of combining the structures of 4-chlorotestosterone and methandrostenolone originated from the chemist Albert Stachowiak. At the time this represented a unique dissociation of anabolic and androgenic effects after oral administration. The product had been introduced for clinical use in 1965.
 
2.Turinabol was developed in the 1960's when East German's were looking for an edge for their Olympic and competitive athletes. It is currently only obtainable through underground labs.O-T, or T-bol as it's sometimes called, is a very nice strength and mass drug, and since it can't convert to estrogen, can even be used on a cutting diet. For this reason, it gets my "most versatile oral" award.
 
3.The user can obtain a hard look to their muscles due to limited water retention.
It is 17-alpha alkylated which means it can be toxic to the liver. Turinabol can also lower the clotting ability of blood.Most users do fairly well with doses between 40 and 60 milligrams per day, taken in divided doses. 
 
4.This is a slower acting steroid.  When using Turinabol, weight, strength and muscle mass increases will not be overly dramatic; however, they will be of good quality. Turinabol also does not typically create risk for estrogenic side effects, so there is limited water retention or risk for gynecomastia. Recently, Oral-Turinabol has found its way back into the hands of athletes all over the world. It's the "new" sexy drug that's actually very old. It was the East German secret weapon when their sports doping program was at it's height.


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add to favorites ... nanjing Other Email:teresa@chembj.com Building Muscle 3381-88-2 Prohormone Superdrol Powders Superdrol
Building Muscle 3381-88-2 Prohormone Superdrol Powders Superdrol 
Email:teresa@chembj.com



Quick Detail:

Product Name Superdrol
CAS 3381-88-2
Synonyms Methyldrostanolone;superdrol;(2alpha,5alpha,17beta)-17-Hydroxy-2,17-dimethylandrostan-3-one;Methasteron;NSC 40490;(2α,5α,17β)-17-Hydroxy-2,17-diMethylandrostan-3-one;17-Methyldrostanolone;17β-Hydroxy-2α,17-diMethyl-5α-androstan-3-one
EINECS 207-098-6
MF C21H34O2
MW 318.49346
mp  223-225ºC
Mol File 3381-88-2.mol
Appearance White crystalline powder
Storage Shading, confined preservation
Packing 1kg/aluminium foil bag or as required
Keywords bodybuilding , steroid hormone , raw material powder
Usage Methasterone is an anabolic androgenic steroid. Methasterone is one of the anabolic steroids screened by the World Anti-Doping Agency (WADA).
Related Substances Pharmaceutical Grade
Place of origin China
Delivery time Within 24 hours upon receipt of payment
Shippment EMS , DHL , TNT , FedEx , UPS
 
Product Description:

1.Superdrol is an anabolic steroid that carries a bit of a unique history compared to many anabolic steroids. Superdrol itself is merely a brand name of an over the counter anabolic steroid sold as a pro hormone or nutritional supplement by Anabolic Extreme. While an anabolic steroid, the active hormone Methyldrostanolone had never been placed on the controlled substance list in the U.S. and in 2005 it would hit the shelves of most major supplement companies and enjoyed massive success. However, in 2006 due to tremendous FDA pressure Superdrol would be discontinued. While the Superdrol brand was short lived, over the counter and black market Methyldrostanolone would continue to appear around the world until mid-2012. In 2012 Methyldrostanolone would be placed on the U.S. controlled substance list and classified as a Schedule III controlled substance along with all anabolic steroids.
2.Methyldrostanolone or Superdrol, while it did not appear on the market until 2005 is not a new anabolic steroid. Syntex first created the Methyldrostanolone hormone in 1959 at the same time as Drostanolone (Masteron) and Oxymetholone (Anadrol). However, the Methyldrostanolone hormone never received a pharmaceutical push like the other two hormones. The exception would be its inclusion in Dimethazine; a compound that metabolically dissolved and converted to Methyldrostanolone post administration. As we dive into the Superdrol compound, as you may have already guessed we will find it is very similar to Drostanolone or the popular anabolic steroid 

Applications:

1.When looking at the effects of Superdrol, the best way to describe the steroid as is a total body transforming product. Through its marketing campaign it was touted as being a more powerful mass builder than Anadrol, hence the name Superdrol; a play on words "Super Anadrol." However, athletes who have used both will attest the effects of Superdrol will in no way lead to mass gains even comparable to Anadrol. However, significant gains in lean tissue can be made so as long as adequate calories are consumed. A gain of 5-10lbs is more than possible and will not be accompanied by the water retention Anadrol often brings. The individual should also find he is able to make cleaner off-season gains due to the effects of Superdrol promoting a stronger metabolism. This is not to say body fat cannot be gained, but you should be able to make better use of your caloric surplus when Superdrol is in play.
2.The effects of Superdrol can also be very beneficial to the dieting athlete as a cutting steroid. This compound will greatly preserve lean tissue during a caloric deficit, a key component to successful dieting. In order to lose body fat we must burn more calories than we consume. This puts lean tissue at risk as the body will take what it needs to meet its energy demands from anywhere it can get it. Due to the body's natural survival instinct, it will often take energy from muscle tissue rather than body fat. The key to successful dieting is ensuring that not only is fat lost but the lean tissue we hold is preserved. The effects of Superdrol will ensure this goal is met. Through the effects of Superdrol the individual should also notice greatly improved conditioning in terms of a dryer, harder look. This isn't all that surprising when we consider this steroid is in many ways oral Masteron, a steroid well known for promoting such traits.
3.Regardless of your reason for use, bulking or cutting, the effects of Superdrol will improve recovery and muscular endurance. We cannot call it the strongest steroid in this regard but the improvements will be significant, and as with all steroids the most important. You will not tire out as fast allowing for work to be done at a maximal level for longer periods of time. This does not mean training time frames need to be increased, but rather they become more efficient. The entire point behind anabolic steroid use is to take what you're already doing right and to simply do it better. Then we have recovery, and this is where the effects of Superdrol as with many anabolic steroids become invaluable. Recovery is where progress is made. Progress isn't actually made in the gym when training. When training we are actually tearing our muscle tissue down, and when we recover this is where it is built, repaired and becomes stronger.


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add to favorites ... nanjing Other Email:teresa@chembj.com 100% Customs Losing Weight 515-69-5 Myrrh Extract Commiphora Momol Extract
100% Customs losing weight 515-69-5 Myrrh Extract Commiphora Momol
Extract  Email:teresa@chembj.com                                       


Quick Detail:

Product Name Myrrh Extract
CAS NO  515-69-5
Einecs No 202-509-5
MF  C15H26O
MW  208-205-9
Purity >99%
Appearance Brown powder
Packing  In fiber-drums with two-plastic bags inside. 
Lead time Within 24 hours upon receipt of payment
Shipment EMS, DHL, TNT, FedEx, UPS
Uses 1)antibacterial action
2) antiatheroscloresis effects
3)losing weight
 
Product Description:

With its smoky, earthy scent, myrrh has a long history as a favorite among all cultures going back to its first discovery in the far reaches of time. A native to Ethiopia and Somalia, it has been used as long ago as 3000 BCE by the Egyptians in embalming, and as an incense burned during cremations and funerals to disguise any foul odors up through the 15th century. Myrrh is said to be one of the key ingredients in the mythical Egyptian perfume Kyphi. It has also been used to anoint kings, and scent fabrics for those traveling to holy places. Myrrh has had a great value throughout time; the Romans even valued it as much as gold, using it as security for monetary debts.

Specification:


Appearance
Brown Powder 

Odor 
Characteristic 

Loss on Drying
≤5%

Assay
5:1, 10:1, 20:1, etc.

Ash
≤5%

Sieve Analysis
≥100mesh

Extract Solvent
Alcohol

Heavy Metal
≤10PPM

Total Plate Count
≤1000cfu/g

Yeast & Mold
≤100cfu/g

E.Coil
Negative

Salmonella
Negative

Application:

Applied in health care  field, it is mainly used health care products.Applied in the field of health care products, it was used in capsules, health food, oral liquid, health care wine and other alcoholic beverages, which has good health-care effect on human cardiovascular and endocrine system, delaying aging


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add to favorites ... nanjing Other Weight Loss API Powder Rimonabant 168273-06-1 Acomplia for Body Shape Email:teresa@chembj.com
Weight Loss API Powder Rimonabant 168273-06-1 Acomplia for Body Shape Email:teresa@chembj.com
 
 
 Quick Details:

Product Name Rimonabant
CAS No 168273-06-1
MF C22H21Cl3N4O
MW 463.79
Mol File 168273-06-1.mol
Assay 99%
Storage temp 2-8°C
Usage Rimonabant is a selective antagonist of CB1 with IC50 of 13.6 nM and EC50 of 17.3 nM in hCB1 transfected HEK 293 membrane
Shipping EMS , FedEx , TNT , DHL , UPS
Delivery Express Courier
Brand Name NJBN STEROID
Appearance White Crystalline Powder
Export Markets Global
Sample Free
Package Discreet and safe packages according to different countries
Product Categories Weight Loss;SR141716
 
 Description:
 
1.Rimonabant is an anorectic anti-obesity drug produced and marketed by Sanofi-Aventis. It is an inverse agonist for the cannabinoid receptor CB1. Its main avenue of effect is reduction in appetite. Rimonabant is the first selective CB1 receptor blocker to be approved for use anywhere in the world. Rimonabant is approved in 38 countries including the E.U., Mexico, and Brazil. It was rejected for approval for use in the United States. This decision was made after a U.S. advisory panel recommended the medicine not be approved because it may increase suicidal thinking and depression.

2.Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.8 nM) to be developed as an appetite suppressant, anti-obesity drug.1 It is widely used as a tool to investigate CB receptor properties and the mechanisms by which CB agonists exert their pharmacological effects. In rodent models and clinical trials, rimonabant effectively induces lipolysis, reduces hepatomegaly, decreases body weight, and improves dyslipidemia by reducing triglyceride, free fatty acid, and total cholesterol levels and by increasing HDL/LDL ratios.2 However, rimonabant reportedly produces adverse psychiatric and neurological effects (e.g., depression or anxiety) and therefore is not approved by the FDA for use as a weight control medication.

3.Rimonabant elicits antiproliferative and immunomodulatory effects (e.g., cell cycle arrest, increased expression of IκB and phosphorylated Akt, and decreased expression of NF-κB, phosphorylated ERK1/2, COX-2, and iNOS) in vitro.3.Rimonabant (Acomplia/Zimulti) is a new drug, the first in its class, indicated for weight loss in obese or overweight patients with co-morbidities. Different trials have also shown that it could improve HbA1c and lipid profiles (increased HDL and reduced triglyceride) in overweight or obese patients. Its use was associated with occurrence of psychiatric adverse events, although most of the patients with various kinds of depressive symptoms did eventually recover with or without anti-depressants drugs. Other common adverse events were anxiety, insomnia, mood alterations with depressive symptoms, depressive disorders, dizziness, nausea, diarrhoea, vomiting, and asthenia/fatigue.

4.Rimonabant was approved in Europe and was first marketed in the UK in 2006. In July 2007, the Committee for Medicinal Products for Human Use (CHMP) recommended some changes to the prescribing information. CHMP recommended that rimonabant not be prescribed in patients with ongoing major depression or in patients taking antidepressants. CHMP also warned that treatment with rimonabant should be stopped if a patient develops depression, including additional information on the psychiatric safety of rimonabant.In November 2008, the marketing authorisation of rimonabant was suspended in all the Member States in which the product was being marketed; and in December 2008, the marketing authorisation holder (MAH) responsible for rimonabant, Sanofi-Aventis, voluntarily withdrew its marketing authorisation. In January 2009, the European Commission withdrew the marketing authorisation for rimonabant on the ground of negative benefit-risk balance based on post-marketing data.
 
 Application:

1.Rimonabant hydrochloride (SR-141716A) is a potent and selective CB1 cannabinoid inverse agonist/antagonist with a Ki of 1.6 nM, minimal affinity for CB2, and and some GPR55 agonist activity. Rimonabant was developed as an anti-obesity drug because of its appetite suppressant activity, but was taken off the market because of side effects of depression and anxiety.

2.Trials of Rimonabant over the last few years have shown it to be an effective weight loss aid for some people. It was found that, of those taking 20mg tablets of Rimonabant, a third lost over 10% of their initial body weight, while over 60% lost over 5%. Average waist measurements are reported to have reduced by between 6 and 9 cm (3-4 inches).Patients followed a low calorie diet while taking the drug, and achieved better results than a control group following a low calorie diet and taking a placebo.Participants in these trials also showed improved glucose control, cholesterol and triglyceride measurements from blood fats. These results show improvements of beyond what is expected from normal weight loss. For this reason, Rimonabant is believed to have positive effects on these measures. High-Density lipoprotein cholesterol (The good cholesterol) measures had also improved beyond expected levels.

3.Rimonabant is used complementary to diet and exercise to treat obese or overweight patients who suffer from Type 2 diabetes and abnormal levels of fat in the blood. It can also prevent the risk of cardiovascular disease.



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add to favorites ... nanjing Other Acromegaly & Gigantism CAS 83150-76-9 Newly Peptide Octreotide Acetate for Bodybuilding Email:teresa@chembj.com
Acromegaly & Gigantism CAS 83150-76-9 Newly Peptide Octreotide Acetate for Bodybuilding Email:teresa@chembj.com


Quick Details :

Product Name : Octreotide Acetate
CAS No. : 83150-76-9
Purity (HPLC) : 98.0%min.
Molecular Formula : C49H66N10O10S2
Molecular Weight : 1019.28
Appearance : White powder
Single Impurity (HPLC) : 1.0%max
Amino Acid Composition : ±10% of theoretical
Peptide Content (N%) : ≥80.0%
Water Content(Karl Fischer) : ≤7.0%
Acetate Content(HPIC)  : ≤12.0%
Specific Rotation (20/D)  : -45.0~-50.0°(c=0.5 95%HAc)
MS (ESI) : Consistent
Mass Balance : 95.0~105.0%
Grade : Pharmaceutical Grade
Storage: Closed, below 2 ~ 8ºC preservation 
Brand Name:NJBN STEROID
Usage : octreotide acetate, as an injectable depot formulation for the treatment of growth hormone producing tumors (acromegaly and gigantism).

Description :

Octreotide (brand name Sandostatin, Novartis Pharmaceuticals) is an octapeptide that mimics natural somatostatin pharmacologically, though it is a more potent inhibitor of hormone, glucagon, and insulin than the natural hormone. It was first synthesized in 1979 by the chemist Wilfried Bauer.

Application :

1.Octreotide has also been used off-label for the treatment of severe, refractory diarrhea from other causes. It is used in toxicology for the treatment of prolonged recurrent hypoglycemia after sulfonylurea and possibly meglitinides overdose. It has also been used with varying degrees of success in infants with nesidioblastosis to help decrease insulin hypersecretion.

2.Octreotide has been used experimentally to treat obesity, particularly obesity caused by lesions in the hunger and satiety centers of the hypothalamus, a region of the brain central to the regulation of food intake and energy expenditure. The circuit begins with an area of the hypothalamus, the arcuate nucleus, that has outputs to the lateral hypothalamus (LH) and ventromedial hypothalamus (VMH), the brain's feeding and satiety centers, respectively.The VMH is sometimes injured by ongoing treatment for acute lymphoblastic leukemia (ALL) or surgery or radiation to treat posterior cranial fossa tumors.


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add to favorites ... nanjing Other 50-41-9 Bodybuilding Steroid Hormone Powder Drostanolone Enanthate for Fat Loss Email:teresa@chembj.com
50-41-9 Bodybuilding Steroid Hormone Powder Drostanolone Enanthate for Fat Loss Email:teresa@chembj.com


Quick Detail:

Product Name Drostanolone Enanthate
Alias Dromostanolone Enanthate
CAS NO 50-41-9
Appearance White crystalline powder
MW 598.08
MF 416.64
Storage Shading, confined preservation
Purity 99%
Synonyms DROSTANOLONE ENANTHATE;Inhouse;Mast E;DroMostanolone Enanthate
Place of origin China
Brand Name NJBN STEROID
Package 1kg/aluminium foil bag or as required
Shipping EMS , DHL , TNT , FedEx , UPS
Delivery time within 24 hours upon receipt of payment.
Usage Pharmaceutical material, Steroid hormone, Anabolic. As a male hormone
and anabolic hormones.
Product Categories Steroid and Hormone
 
Product Description:

1.Drostanolone Enanthate, is a commonly used steroid that has properties similar to dihydrotestosterone and does not lead to aromatization. Drostanolone Enanthate is very popular among sportsmen and fitness-conscious individuals who want to retain strength while losing body fat. Drostanolone enanthate, which also may be called Masteril or Masteron, is an anabolic steroid. Drostanolone enanthate is used primarily by athletes who need to retain strength while losing mass. It is beneficial to runners and athletes who must remain in a certain weight class. Drostanolone enanthate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.
2.Drostanolone enanthate is one of the best anabolic steroids for promoting muscle function and definition and inhibiting the transformation of free testosterone to estrogen, which enhances the rate of free testosterone circulating in the body.Drostanolone Enanthate is the anabolic steroid that is slow acting, but is acts for longer period of time. In fact, Masteron Enanthate comes with an ester, Enanthate attached to the drostanolone, and Enanthate is responsible for slower, but longer release of hormone.

Applications:

1.Drostanolone enanthate is one of the best anabolic steroids for promoting muscle function and definition and inhibiting the transformation of free testosterone to estrogen, which enhances the rate of free testosterone circulating in the body.Since the propionate ester is used with this compound, injections need to be repeated at least every 3 or 4 days in order to maintain a consistent level of hormone in the blood. The weekly dosage is in the range of 300-500mg.Since estrogen is not an issue, side effects are generally mild with this steroid. As discussed earlier, gynecomastia, water retention, and high blood pressureare not a problem. Masteron is also not liver toxic, so there is little concern stress will be placed on this organ, even during longer cycles. The only real side effects would be from the basic androgenic properties of dihydrotestosterone. Drostanolone enanthate, which also may be called Masteril or Masteron,is an anabolic steroid.
2.Drostanolone enanthate is used primarily by athletes who need to retain strength while losing mass. It is beneficial to runners and athletes who must remain in a certain weight class.Drostanolone enanthate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.Drostanolone enanthate can promote increased strength while keeping body fat the same or even lowering it, something can help to prevent muscle loss while dieting.



Hi,I'm teresa,everybody is taking the similar words,what I want to say is:Just give me a chance,Just have a try on me,maybe you will get a big surprise on me,come to join us,Buddy!


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Whatsapp:+86-17327095740

Email:teresa@chembj.com
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