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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.



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add to favorites ... nanjing Other Email:teresa@chembj.com High Purity GMP Grade Sarms Powder CAS 317318-84-6 Gw610742/Gw-0742
High Purity GMP Grade Sarms Powder CAS 317318-84-6 Gw610742/Gw-0742 Email:teresa@chembj.com


 Quick Detail:

Product name GW0742
Synonyms GW0742;[4-[[[2-[3-FLUORO-4-(TRIFLUOROMETHYL)PHENYL]-4-METHYL-5-THIAZOLYL]METHYL]THIO]-2-METHYLPHENOXY]ACETIC ACID;4-[2-(3-FLUORO-4-TRIFLUOROMETHYL-PHENYL)-4-METHYL-THIAZOL-5-YLMETHYLSULFANYL]-2-METHYL-PHENOXY-ACETIC ACID
CAS No 317318-84-6
Alias Nolvadex,STERANABOL;TURINABOL,kessar; noltam
EINECS 259-415-2
MF C21H17F4NO3S2
MW 471.49
Appearance Light Yellow Solid
Assay 99%
Storage Shading, confined preservation
Drug Class Anabolic Androgenic Steroid 
Delivery time within 24 hours upon receipt of payment
Delivery EMS, DHL, TNT, FedEx, UPS
Brand NJBN STEROID
Usage A small molecule agonist of the human Peroxisome Proliferator-Activated Recept δ (PPAR δ). It shows an EC50 of 1.1 nM against PPAR δ with 100-fold selectivity over the other human subtypes.
 
Product Description:

1.GW0742 is a synthetic, potent and selective PPAR-β/δ agonist. PPARs are ligand-dependent transcription factors which are involved in many physiological processes, such as inflammation and energy homeostasis. PPAR-β/δ is one of three PPARs in the nuclear hormone receptor superfamily that are collectively involved in the control of lipid homoeostasis among other functions. GW0742 can attenuate the increase of PARP activity that caused by SAO shock. GW0742 is also able to prevent radiation-induced brain injury in C57Bl/6 wild-type (WT) and PPARδ knockout (KO) mice. Dietary GW0742 can prevent the acute increase in IL-1β mRNA and ERK phosphorylation measured at 3 h after a single 10-Gy dose of WBI as well as the increase in the number of activated hippocampal microglia 1 week after WBI.

2.GW0742 is a synthetic high affinity PPAR β/δ agonist, and its possible role in preventing the advance of inflammatory and apoptotic processes induced by bleomycin, that long-term leads to the appearance of pulmonary fibrosis. Our data showed that GW0742-treatment (0.3 mg/Kg, 10 percent DMSO, i.p.) has therapeutic effects on pulmonary damage, decreasing many inflammatory and apoptotic parameters detected by measurement of: 1) cytokine production; 2) leukocyte accumulation, indirectly measured as decrease of myeloperoxidase (MPO) activity; 3) IkBα degradation and NF-kB nuclear translocation; 4) ERK phosphorylation; 5) stress oxidative by NO formation due to iNOS expression; 6) nitrotyrosine and PAR localization; 7) the degree of apoptosis, evaluated by Bax and Bcl-2 balance, FAS ligand expression and TUNEL staining. Taken together, our results clearly show that GW0742 reduces the lung injury and inflammation due to the intratracheal BLEO--instillation in mice.

Applications:

According to our previous method,16 the stock solutions of agonist GW0742 (Tocris Bioscience, Bristol, UK) or antagonist GSK0660 (Tocris Bioscience) were prepared in dimethyl sulfoxide. A fresh solution diluted with 9% normal saline to the indicated dose was used to treat the animals. To rule out the pharmacokinetic factors, GW0742 was intravenously injected at the indicated dose into animals under anesthesia. Additionally, GSK0660 was similarly injected 30 minutes before the injection of GW0742. The changes were then used to compare with the control, which was treated with the same volume of vehicle.


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add to favorites ... nanjing Other Email:teresa@chembj.com Bodybuilders Peptide Powder 170851-70-4 Energy Homeostasis & Regulation of Bodyweight Ipamorelin
Bodybuilders Peptide Powder 170851-70-4 Energy Homeostasis & Regulation of Bodyweight Ipamorelin
Email:teresa@chembj.com


Quick Details :

Product Name:Ipamorelin
Alias : 696: PN:WO2004005342 PAGE: 46 claimed protein, Ipamorelin, NNC 26-0161
CAS: 170851-70-4
Formula: C38H49N9O5
MW:711.853
Appearance: White powder
Grade : Pharmaceutical Grade
Brand Name:NJBNSTEROID
purity:99%min
Usage :Growth hormone secretagogue receptor is a G protein-coupled receptorthat binds ghrelin and plays a role in energy homeostasis and regulation of bodyweight.

Description:

Ipamorelinis a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. Like the GHRP-6 peptide (growth hormone releasing hexapeptide), it is a synthetic peptide that has powerful Growth Hormone releasing properties. And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat.

Application :

1.Ipamorelin is an interesting peptide taken 300mcg twice daily or you could lower the dose for 3 times daily, side effects are head rushs, I would recommend taking this 30 minutes before workout ,with gear, Ipamorelin is a new and potent synthetic pentapeptide which has distinct and specific growth hormone (GH)-releasing properties. With the objective of investigating the effects on longitudinal bone growth rate , body weight , and GH release, Ipamorelin in different doses (0, 18, 90 and 450 μg/day) was injected three times daily for 15 days to test subjects, After intravital Tetracycline labelling on days 0, 6, and 13, LGR was determined by measuring the distance between the respective fluorescent bands in the proximal tibia metaphysis.

2.Ipamorelin dose-dependently increased LGR from 42 μm/day in the vehicle group to 44, 50, and 52 μm/day in the treatment groups . There was also a pronounced and dose-dependent effect on body weight gain. The treatment did not affect total IGF-I levels, or serum markers of bone formation and resorption. The number of tartrate-resistant acid phosphatase-positive multinuclear cells in the metaphysis of the tibia did not change significantly with treatment. The responsiveness of the pituitary to a provocative i.v. dose of Ipamorelin or GHRH showed that the plasma GH response was marginally reduced , after Ipamorelin, but unchanged after GHRH. The pituitary GH content was unchanged by Ipamorelin treatment. Whether Ipamorelin or other GH secretagogues may have a place in the treatment of children with growth retardation requires demonstration in future clinical studies. Before closing Ipamorelin is the most selective GH releaser you can get.

3.Ipamorelin doesn't create bumps in either prolactin or cortisol like GHRP-2 and -6. Ipa is a rifle bullet, not a shotgun blast like other GHRP's. Also it's great for those on relatively calorie restricted diets because it doesn't stimulate appetite

4.Ipamorelin and Peptides are the way of the future ,expect in the next 5 years or less a dramatic change in the way we train and take the bodybuilding world by storm.


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add to favorites ... nanjing Other Email:teresa@chembj.com CAS 317318-70-0 Anabolic Steroid Sarms Cardarine Hormone Gw-501516
CAS 317318-70-0 Anabolic Steroid Sarms Cardarine Hormone GW-501516 Email:teresa@chembj.com


Quick Detail:

Product Name GW-501516
Synonyms 2-(4-((2-(4-(TRIFLUOROMETHYL)PHENYL)-5-METHYLTHIAZOL-4-YL)METHYLTHIO)-2-METHYLPHENOXY)ACETIC ACID;2-[2-Methyl-4-[[[4-methyl2[4(trifluoromethyl)phenyl]-5thiazolyl]methyl]thio]phenoxy]acetic Acid;Methyl-methyl-trifluoromethylphenyl -thiazolyl-methylsulfanyl-phenoxy-acetic Acid;2-(4-((2-(4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methylthio)-2-methylphenoxy)acetic acid;GW 1516;2-(2-methyl-4-((5-methyl-2-(4-(trifluoromethyl)phenyl)thiazol-4-yl)methylthio)phenoxy)acetic acid;GW501516, Free Acid;GSK-516
CAS No 317318-70-0
Assay 99%
MF C21H18F3NO3S2
MW 453.5
Mol File 317318-70-0.mol
mp  134-136°C
storage temp Refrigerator
Stability Light Sensitive
Appearance White Solid
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
Usage An experimental drug meant to control lipids and increase the level of HDL, or good cholesterol, in the bloodstream. A cell-permeable, thiazolyl compound that acts as a potent, high affinity, PPARd agonist. Exhibits selectivity for PPARd compared 
 
 Product Description:

1.GW501516 (GW1516 or GSK-516) is a drug that acts as a PPARδ modulator. GW 501516 activates AMP-activated protein kinase and stimulates glucose uptake in skeletal muscle tissue, and GW 501516 has been demonstrated to reverse metabolic abnormalities in obese men with pre-diabetic metabolic syndrome, most likely by stimulating fatty acid oxidation. It has been proposed as a potential treatment for obesity and related conditions, especially when used in conjunction with a synergistic compound AICAR, as the combination has been shown to significantly increase exercise endurance in animal studies.
2.How it works:GW501516 is a selective agonist (activator) of the PPARδ receptor. It displays high affinity (Ki = 1 nM) and potency (EC50 = 1 nM) for PPARδ with > 1000 fold selectivity over PPARα and PPARγ.In rats, binding of GW501516 to PPARδ recruits the co activator PGC-1a. The PPARδ/coactivator complex in turn up regulates the expression of proteins involved in energy expenditure. Furthermore in rats treated with GW501516, increased fatty acid metabolism in skeletal muscle and protection against diet-induced obesity and type II diabetes was observed. In obese rhesus monkeys, GW501516 increased high-density lipoprotein (HDL) and lowered very-low-density lipoprotein (VLDL). The mechanism by which PPARδ agonists increase HDL appears to be a result of increased expression of the cholesterol transporter ABCA1.
3.Uses:there are two main uses with GW-501516. The first and most common use is that of increased endurance. GW has been banned for professional athletes due to the unfair advantage it provides to endurance athletes. Anyone want a drastic increase in endurance will find that GW truly shines in this aspect. It takes effect very quickly and the results can be staggering. A common dose of 10 mg day will provide a significant increase in endurance.
4.The second common usage with GW is that of fat loss. Many users turn to GW as it has shown to melt off fat while still being non-catabolic. You will find that you can still hold on to some muscle as you are losing fat. It helps when you are running it in conjunction with SARMS Ostarine and S4, to hold on to as much muscle as possible. A dosage of 10 mg a day will provide good amounts of fat loss, but an increase to 20 mg a day will provide much more in this area.GW 501516 can be ran in 8 week cycles, but as with any other steroid or supplement, it should be cycled properly to avoid any possible side effects and the keep it as effective as possible.
 
  Applications:

1.GW has many benefits but has two primary uses. The most common use of GW consists of the extreme amount of endurance and recovery increase. The results with GW use regarding endurance increase are staggering. GW was banned by the WADA (World Anti Doping Association) in 2009 because it provided such a large advantage to its user over the competition. GW acts quickly and the results are drastic. A user can expect to see an endurance increase within a few days of use. The common dosage for these types of results are 10 mg a day but can be taken up to 20 mg a day. Either way, a significant increase in endurance will occur.
2.The other main use of GW is to aid in fat loss. GW has shown to melt away fat at a rapid pace. Another strong component of GW is that it is non catabolic, meaning it allows a user to lose fat and not have to sacrifice muscle. Many people that are on a diet burning fat are also sacrificing a lot of muscle, but GW allows a user to hold on to much more muscle than a standar fat lass diet or other fat loss compound would allow. GW also shines when ran in conjunction with other SARMS. When stacking GW with Ostarine and S4, users can add lean muscle while still losing weight and body fat. This makes GW highly desirable for many. The most optimal dosage for fat loss is 20 mg a day but users will still be able to receive this benefit at 10 mg a day.
3.GW 501516 can be ran in 8-12 cycles and can also b ran in conjunction with any SARM, steroid or supplement. As with any other steroid or supplement, it should be cycled properly to avoid any possible side effects and the keep it as effective as possible.


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add to favorites ... nanjing Other Email:teresa@chembj.com Best Peptide Top Purity CAS 60731-46-6 Elcatonin for Hypercalcemia & Osteoporosis
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Quick Details:

Product Name:Elcatonin
Alias:Calcinil,Carbicalcin,Carbocalcitonin,Elcatonin, Elcitonin, Turbocalcin,[Aminosuberic acid1,7]-eel calcitonin
CAS NO. : 60731-46-6
EINECS : 262-393-7
MF : C148H244N42O47
MW : 3363.82
Appearance : White powder
Manufacturer : Hezhong
Purity : 98%
Grade : Pharmaceutical Grade
Peptide Content(by %N): ≥80%
Water Content(Karl Fischer): ≤8.0%
Acetate Content(by HPLC): ≤12.0%
Amino Acid Composition: ±10% of theoretical
Purity(by HPLC): 98.0%min.
Single Impurity(by HPLC): 0.5%max.
Assay(By Anhydrous, Acetic Acid-free): 95.0~105.0%
MS: Consistent
Packing: plastic vial(dedicated for peptide packing) or glass vial, quantity according to customer's detail requirement.
Storage: Cool dry place(-20ºC, away from the light)
Usage : Elcatonin is used for Hypercalcemia, osteoporosis.
 
Description:

Elcatonin is a Calcitonin derivative which is transformed from eel's calcitonin by changing the S-S bond into the stable C-N bond. It inhibits the absorption and autolysis of bones, thus leads to blood calcium descending. In addition, it inhibits the bone salts dissolving and transferring and promotes the excretion of calcium and phosphorus in urine. Meanwhile, it inhibits renal tubules reabsorbing calcium, phosphorus and sodium and keeps blood calcium at normal level. It is mainly used for remitting or eliminating the pain caused by Osteoporosis.
 
Application:
 
As a kind of Electrolyte supplement. Elcatonin is a calcitonin derivative used as an anti-parathyroid agent. Specific application ways are listed as following:
1.) Take an alcohol swab to the stopper of both your peptide vial and the vial of the dilutent.
2.) With a 1cc syringe and draw your preferred dilutent. Choose an amount that will make measuring the final product simple.
1ml(cc) per 10mg vial of Melanotan would mean each 10 mark on a U100 slin syringe would equal 1mg of Melanotan
1ml(cc) per 10 IU vial of would mean each 10 mark on a U100 slin syringe would equal 1 IU of HGH
2ml(cc) per 10mg vial of Melanotan would mean each 10 mark on a U100 slin syringe would equal 1mg of Melanotan
2ml(cc) added to a 10 IU vial of would mean that the 20 mark on a U100 syringe would equal 1 IU of HGH
3.) Take the syringe with the dilutent and push it into the vial of lyophilized powder letting the dilutent dissolve the peptide.
4.) After all of the dilutent has been added to the vial, gentling swirl (do NOT agitate or violently shake the vial) until the lyophilized powder has dissolved and you are left with a clear liquid. The peptide is now ready for use. Store your now reconstituted peptide in the refrigerator.


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add to favorites ... nanjing Other Email:teresa@chembj.com Ostarine Enhanced Libido 1202044-20-9 Anabolic Steroids Hormone Powder Mk-2866
Ostarine Enhanced Libido 1202044-20-9 Anabolic Steroids Hormone Powder MK-2866 Email:teresa@chembj.com


Quick Details:

Product Name MK-2866
Synonyms Ostarine(MK-2866);MK-2866 Ostarine;(2S)-3-(4-Cyanophenoxy-2,3,5,6-d4)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide;((2s)-3-(4-cyanophenoxy)-N-[4-cyano-3-(trifluoroMethyl)phenyl]-2-hydroxy-2-MethylpropanaMide);Ostarine (MK-2866, GTx-024)
CAS NO 1202044-20-9
Assay 99%
Appearance white crystalline power
MF C19H10D4F3N3O3
MW 247.2715
Storage Shading, confined preservation
Related Substances Pharmaceutical Grade
Brand NJBN STEROID
Usage  including enhanced libido, better endurance, and stronger gains
 
Product Description:

1.Ostarine is a SARM known for its ability to give you steroid-like benefits. Unlike with traditional anabolic steroids, SARMs target androgen receptors (they don't just flood your body with hormones). This raises your growth factor hormones in an indirect - but extremely effective - way.
2.Ostarine is arguably the most controversial SARM on the market today. It's controversial because it was the first SARM to be the subject of a lawsuit - one Ostarine retailer was sued by its competitor for marketing Ostarine supplements as nutritional supplements when they should probably be marketed as "drugs" and be under the jurisdiction of the FDA (see the lawsuit section below for more information).
3.Today, Ostarine can be taken in oral form or via injection. Chemically speaking, Ostarine's formula looks like this:((2S)-3-(4-cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide)
Depending on where you're looking, Ostarine can go by a number of different names, including:
- Enobasarm
- GTx-024
- MK-2866

 Applications:

Another reason why ostarine is so popular among bodybuilders and powerlifters, is that it has some noticeable abilities to strengthen bones and joints. This is a very important trait, since athletes may run into such nagging injuries as forearm or shin splints, neck pain, joint pain, back pain and many other injuries that never seem to go away. Unfortunately, many athletes make the mistake of taking harmful drugs to dull or kill the pain, which is merely a band aid, and on the long run this kind of abuse will make the injury go chronic and permanent.
However, ostarine can work its magic by increasing tendon strength, ligament strength, and bone density at a dose under 20 milligrams (mg) per day. Moreover, it doesn't merely cover up the problem - ostarine actually fixes it. Thus, athletes will be satisfied with ostarine's healing effects on their inflamed joints.


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add to favorites ... nanjing Other Email:teresa@chembj.com CAS 859-18-7 Pharmaceutical Raw Materials Lincomycin Hydrochloride of Veterinary Medicine
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CAS 859-18-7 Pharmaceutical Raw Materials Lincomycin Hydrochloride of  Veterinary Medicine Email:teresa@chembj.com


Quick Details:

Product Name:Lincomycin hydrochloride
Alias: Lincomycin HCL, Lincomycin, Lincocin
CAS Registry Number:859-18-7
Assay:99%
Formula:C18H34N2O6S.HCl
Molecular Weight:443.06
EINECS: 212-726-7
Appearance:white powder
Related Substances : Pharmaceutical Grade
Storage: Shading, confined preservation
Brand Name:NJBN STEROID
Usage:Anesthetic Agents, Anti-Allergic Agents
 
Applications:

1.Lincomycin is a lincosamide antibiotic that comes from the actinomyces Streptomyces lincolnensis.A related compound,  is derived from lincomycin by using thionyl chloride to replace the 7-hydroxy group with a chlorine atom with inversion of chirality.A two-hour intravenous infusion of 600 mg of Lincomycin achieves average peak serum levels of 15.9 micrograms/ml and yields therapeutic levels for 14 hours for most susceptible gram-positive organisms. Urinary excretion ranges from 4.9 to 30.3 percent (mean: 13.8 percent).
 
2.Although similar in structure, antibacterial spectrum, and mechanism of action to macrolides, lincomycin is also effective against other organisms including actinomycetes, mycoplasma, and some species of Plasmodium.Intramuscular administration of a single dose of 600 mg of Lincomycin produces average peak serum levels of 11.6 micrograms/ml at 60 minutes, and maintains therapeutic levels for 17 to 20 hours, for most susceptible gram-positive organisms. Urinary excretion after this dose ranges from 1.8 to 24.8 percent (mean: 17.3 percent).
 
3.The biological half-life after IM or IV administration is 5.4 ± 1.0 hours. The serum half-life of lincomycin may be prolonged in patients with severe impairment of renal function, compared to patients with normal renal function. In patients with abnormal hepatic function, serum half-life may be twofold longer than in patients with normal hepatic function. Hemodialysis and peritoneal dialysis are not effective in removing lincomycin from the serum.Tissue level studies indicate that bile is an important route of excretion. Significant levels have been demonstrated in the majority of body tissues. Although lincomycin appears to diffuse in the cerebrospinal fluid (CSF), levels of lincomycin in the CSF appear inadequate for the treatment of meningitis.


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add to favorites ... nanjing Other Factory Direct Sales 112568-12-4 Liomyoma Extracellular Matrix Potential Application Antide Email:teresa@chembj.com
Factory Direct Sales 112568-12-4 Liomyoma Extracellular Matrix Potential Application Antide 


Quick details :

Product Name:Antide
Alias: D 21074, Iturelix, ORF 23541
CAS NO.: 112568-12-4
MF : C82H108ClN17O14
MW : 1591.29
Appearance : Sterile Filtered White lyophilized (freeze-dried) powder.
Grade :Pharmaceutical Grade
Brand Name:NJBN STEROID
Formulation : The Antide peptide was lyophilized with no additives.
Solubility : It is recommended to reconstitute the lyophilized Antide in sterile water + acetonitrile not less than 100 µg/ml, which can then be further diluted to other aqueous solutions.
Stability : Lyophilized Antide although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon reconstitution Antide should be stored at 4°C between 2-7 days and for future use below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
Please prevent freeze-thaw cycles.
Purity : ≥94.0% as determined by RP-HPLC.
Amino acid sequence : Antide has a molecular formula of C82H108N17O14 Cl1, a.a. sequence of Ac-D-2-Nal-D-Phe(4-CL)-3-D-Pal-Ser-Lys(nicotinoyl)-D-Lys(nicotinoyl)-Leu-Lys(Isopropyl)-Pro-D-Ala-Nh2.
Usage: ProSpec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
 
Description :
 
1.Antide acetate (Ac-AA10-NH2) is an LHRH antagonist and represses LH and FSH release from the pituitary gland. Antide.Antide acetate is a peptide which acts as an LHRH antagonist in 'natural settings' and can be utilized by an animal's body to represses FSH and LH releases that stem from the pituitary gland. Synthetic versions of this chemical have been developed as a means of controlling these reactions in a laboratory setting, both as a means to determine a potential medical use for antide acetate and to help researchers better understand the role of this chemical in an animal's body when it is naturally produced.
 
Application :
 
Antide acetate that is prepared for use in a laboratory setting is provided in a lyophilized sterile condition that can be reconstituted or diluted with an aqueous solution as necessary for the given application. Researchers are encouraged to seek out a supply that is prepared without additives, to ensure accurate and reliable testing results once the chemical is in use.Protein quantitation via analysis of the calibrated solution of the chemical or UV spectroscopy set to 280 nm is recommended when applicable.


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