Pharmaceutical raw materials used in synthesizing new medications

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lymphocyte antigen 6 complex locus K (119-128) LAB GRADE 97%

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Hyaluronan mediated motility receptor (165-173) LAB GRADE 97%

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Muscle Building Steroids Powder Epistane Methyl E 4267-80-5

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Muscle Building Steroids Powder Epistane Methyl E 4267-80-5
 
Epistane Basic Info.
 
Product name: Epistane
Alias: Methyl Epitiostanol
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Sulfur & Selenium Compounds
CAS: 4267-80-5
M.F.: C20H32OS
Assay: 98%
M.P.: 168-169°C
Appearance: White powder
Package: foil bag
Usage: Epistane is a methylated derivative of the steroid epitiostanol (E588800). Epistane is a readily orally active compound that lacks the 3-ketone common to most anabolic steroids. Epistane greatly incr eases protein synthesis and build up in lean muscle mass
 
Epistane Description:
 
Epistane, exhibits a strong, long lasting anti-estrogen effect that is organ tissue specific. This means it works only where you want it to work. Broad range estrogen blockers and aromatase inhibitors can result in system shut down, aching joints, and decreased IGF-I expression. Epistane binds specifically to the 17-estradiol receptor protein in the target tissues. Because of its long lasting and strong effects on specific tissue,
 
Epistane can significantly reduce and reverse the effects of gynocomastia because not only does Epistane specifically block estrogen in breast tissue but it induces an estrogen-depleted condition which leads to apoptosis or the death of the breast tissue cells. Studies show that small doses of the parent compound, Epitiostanol, at just 10-20mg/week showed a complete disappearance of the mass and pain in 25% of the male patients in the clinical trail, while the other 75% of the patients showed at least a 50% reduction in the mass and complete loss of pain in just 4-8 weeks. Thats results in 100% of the male users with no side effects.
 
Epistane is more than an anti-estrogen, though, as it also binds to androgen receptors in skeletal muscle. As a PRO-Anabolic compound Epistane promotes increases in strength and lean body mass with an anabolic/androgenic value (Q ratio) of 12. With most powerful androgens there is a high risk of the natural suppression of the gonads. Epistane, unlike other PRO-Anabolic compounds that have recently been released, is relatively mild on the gonads and, due to the anti-estrogenic effects and the fact that Epistane keeps LH levels elevated, post cycle therapy becomes a breeze.
 
Application Of Epistane:
 
Epistane is a DHT derived prohormone that was brought to market by RPN with their product "Havoc. " Epistane is an anti-estrogenic dry compound that will aid users in adding lean muscle mass as well as cutting fat. In addition to this, Epistane does not aromatize and is non-progestagenic. This basically means that while on Epistane, estrogen related side effects like gyno and progesterone related side effects like sensitive breast tissue are virtually non-existent. Users will experience little to no side effects while on Epistane, making it an ideal beginner prohormone.
 
Epistane Function:
 
Epistane also binds to androgen receptors in skeletal muscle cells and muscle stem cells. This leads to changes in muscle cell function and protein synthesis. In the case of muscle stem cells, which will actually change and fuse with your active adult skeletal muscles increasing the muscles potential for growth and repair. On the opposite side, the presence of androgens actually decreases the ability of stem cells to form new fat cells. So now have increased stem cell conversion to muscle cells and decrease the conversion of stem cells to fat cells, giving you more positive effects of nutrition and training.
 

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NATNVIFSRCRDEMF M WD repeat domain 16 (145-175) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply NATNVIFSRCRDEMF M
WD repeat domain 16 (145-175).http://www.creative-peptides.com/product/natnvifsrcrdemf-m-wd-repeat-domain-item-ta-164-11311.html

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Polycystic kidney disease 1 protein (4192-4202) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Polycystic kidney disease 1 protein (4192-4202).http://www.creative-peptides.com/product/polycystic-kidney-disease-protein-item-ta-162-11173.html

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Receptor tyrosine-protein kinase erbB-2 (48-56) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Receptor tyrosine-protein kinase erbB-2 (48-56).http://www.creative-peptides.com/product/receptor-tyrosine-protein-kinase-erbb-item-ta-338-23124.html

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Receptor tyrosine-protein kinase erbB-2 (63-71) LAB GRADE 97%

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis 
 
Pirfenidone Basic information
 
Product Name: Pirfenidone
Synonyms: 5-methyl-1-phenyl-2(1h)-pyridon;amr-69;PIRFENIDONE;5-METHYL-1-PHENYL-1H-PYRIDIN-2-ONE;5-METHYL-1-PHENYL-2(1H)-PYRIDINONE;5-METHYL-1-PHENYL-2-(1H)-PYRIDONE;5-Methyl-N-phenyl-2-1H-pyridone;Pirfenidone also see 5-Methyl-1-Phenyl-2(1H)-Pyridinone
CAS: 53179-13-8
MF: C12H11NO
MW: 185.22
EINECS: N/A
Melting point: 96-97°C
Storage temp.: Store at RT
Solubility: DMSO: ≥10 mg/mL, Soluble
Chemical Properties: Off-White Solid
Usage: Pirfenidone has demonstrated activity in multiple fibrotic conditions, including those of the lung, kidney and liver
Product Categories: Aromatics Compounds;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Cytokine signaling;Inhibitors.
 
Pirfenidone Description:
 
Pirfenidone (INN, BAN) is an anti-fibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). It works by reducing lung fibrosis through downregulation of the production of growth factors and procollagens I and II.
 
It is a drug developed by several companies worldwide, including InterMune Inc. (now part of Roche), Shionogi Ltd., and GNI Group Ltd. In 2008, it was first approved in Japan for the treatment of IPF after clinical trials, under the trade name of Pirespa by Shionogi & Co. In October 2010, the Indian Company Cipla launched it as Pirfenex. In 2011, it was approved for use in Europe for IPF; it was approved in Canada in 2012 ; and was approved in the United States in October 2014 under the same name. In September 2011, the Chinese State Food and Drug Administration provided GNI Group Ltd with new drug approval of pirfenidone in China, and later manufacture approval in 2013 under the trade name of Etuary.
 
In 2014 it was approved in Mexico under the name KitosCell LP, indicated for pulmonary fibrosis and liver fibrosis.There is also a topical form created for the treatment of abnormal wound healing processes.
 
Pirfenidone Application:
 
In vitro, pirfenidone can inhibit the uterine flesh tumour cells and leiomyoma cells proliferation. Pirfenidone can inhibit the TGF - beta - 1 inducing fibroblast collagen formation. Inhibition of PDGF, FGF and TGF - beta - 1 inducing fibroblast proliferation. In hamster model, pirfenidone, taken by mouth, that can the prevention and treatment of pulmonary fibrosis . Pirfenidone can prevent the sclerosing peritonitis in rats induced by chemical, can also be keloid grafting for the treatment of nude mice. Pirfenidone 0.01 1 mg/ml can suppress the matrix and dose dependent manner serum stimulate uterine fibroids and leiomyoma cell DNA synthesis, the compound has no cytotoxic effect, has no effect on collagen mRNA level also. Pirfenidone in hamster pulmonary fibrosis model can reduce the disease before the collagen I mRNA level enhancement, reduce the level of the lung hydroxyproline and malondialadehyde and lung preserved ammonia acyl hydroxylase activity.
 

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Serine/threonine-protein kinase B-raf (586-614) LAB GRADE 97%

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Tau Peptide (255-314) (Repeat 2 Domain) (human) LAB GRADE 98%

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