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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1
 
Andarine Basic Info:
 
Product name: Andarine
Synonyms: Andarine;S4;S-4;GTX-007
CAS No.: 401900-40-1
MF: C19H18F3N3O6
MW: 441.36
Purity: 99.92%
Product categories APIs; Amines; Aromatics; Chiral Reagents; Intermediates & Fine Chemicals; Pharmaceuticals; SARMS
Appearance: White crystalline powder
Natural Bodybuilding SARM Powder Andarine S4 GTX-007 High Purity CAS 401900-40-1
 
Andarine Description:
 
Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs like anabolic steroids but be much more selective in their action, allowing them to be used for many more clinical indications than the relatively limited legitimate uses that anabolic steroids are currently approved for.
 
S-4 is an experimental or investigation-stage proprietary SARM research chemical developed by GTx Inc for treatment of benign prostatic hypertrophy, muscle wasting, and osteoporosis. S-4 is considered a partial agonist of the androgen receptors in target tissue. S-4 has less pronounced anabolic and androgenic compared to other SARMs. In trials treating BPH induced in animal models, S-4 reduced prostate weight as effectively as finasteride and without producing any reduction in muscle mass or other side effects common with androgen receptor binding compounds. Gao et al suggest that by binding to androgen receptors, S-4 prevents DHT from binding and activating, but bypasses the expected anti-androgenic effects that would occur from occupying androgen receptors due to the fact that S-4 itself is a partial agonist of androgen receptors. S-4 has also been shown to prevent bone loss, reduce body fat, and improve muscle strength and body composition in orchidectomized and ovariectomized rats.
 
Andarine Application:
 
S4 Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.
 
Andarine Function:
 
1. 1/3 as androgenic as testosterone in muscle tissue.
2. Anabolic at doses above 50mg.
3. Great for strength.
4. Great for muscle hardness.
5. Great for enhanced vascularity.
6. Great for endurance (aerobic or anaerobic).
7. Accelerated fat loss above 50mg.
8. Joint healing effects.
 

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8
 
PT 141 Basic Info.
 
Product Name: PT-141; PT141
CAS: 32780-32-8
MF: C50H69N15O10
MW: 1040.17736
Appearance: White powder
Water Content(Karl Fischer): ≤ 5.0%
Acetate Content(by HPLC): ≤ 15.0%
Amino Acid Composition: ± 10% of theoretical
Purity(by HPLC): ≥ 97.0%
Single Impurity(by HPLC): ≤ 1.0%
Peptide Content(by %N): ≥ 80%
Assay(By Anhydrous, Acetic Acid-free): 95.0~105.0%
Bacterial Endotoxins: ≤ 5EU/mg
Grade: Pharmceutical Grade
Storage: Shading, confined preservation
 
PT 141 Description:
 
PT-141 is a synthetic amino acid protein discovered during clinical trials using the Melanotan 2 for sunless tanning, photo-protection results from melanotans. Participants were documented as having experienced aphrodisiac reactions, leading to the further development PT-141. The melanocortin system targets receptors associated with desire through the melanocyte stimulating hormone paths that cross the blood-brain-barrier. Potentially the powerful sex-drug results feeling an aphrodisiac experience amplifying arousal pt141 reviews have shown the ability to increase libido effects of both men and women.
 
PT 141 Application:
 
PT-141 functions by activating the melanocortin receptor and MC4R namely. Bremelanotide originally was tested for nasal spray delivery but was discontinued after concerns about side effects. Bremelanotide PT141, as Melanotan II, may cause spontaneous arousal enhancing effect. Unlike other supplements, PT-141 results do not act on the vascular body, but directly increases desires through the nervous system.
 

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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6

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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6
 
3,5-Diiodo-L-Thyronine Basic Information:
 
Product Name: 3,5-Diiodo-L-Thyronine
Synonyms: T2;Diiodothyronine;3,5-Diiodo-L-Thyronine;3,5-Diiodothyronine;
CAS: 1041-01-6
MF: C15H13I2NO4
MW: 525.08
EINECS: 213-867-7
Melting point: 255-260°C (dec.)
Storage temp.: 2-8°C
Chemical Properties: Off-White Solid
Product Categories: Medicine intermediate;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Intermediates;Labeling and Diagnostics Reagents
Usage: Of interest for the early detection and treatment of congenital or drug-induced hypothyroidism.
 

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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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Secretin

Secretin is a hormone that controls the secretions into the duodenum, and also separately, water homeostasis throughout the body. It is produced in the S cells of the duodenum in the crypts of Lieberkuhn.Its effect is to regulate the pH of the duodenal contents via the control of gastric acid secretion and buffering with bicarbonate from the centroacinar cells of the pancreas as well as intercalated ducts.Secretin is released into circulation and/or intestinal lumen in response to low duodenal pH that ranges between 2 and 4.5 depending on species.It increases watery bicarbonate solution from pancreatic duct epithelium,counteracts blood glucose concentration spikes by triggering increased insulin release from pancreas, following oral glucose intake.Secretin has been widely used in medical field especially in pancreatic functioning test because it increases pancreatic secretions.Secretin modulates water and electrolyte transport in pancreatic duct cells,liver cholangiocytes,and epididymis epithelial cells. It has also been recently been found to play a role in the vasopressin-independent regulation of renal water reabsorption.

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Sell Pharmaceutical Grade Plant Extract Glabridin Powder In Cosmetic Industry 59870-68-7

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Sell Pharmaceutical Grade Plant Extract Glabridin Powder In Cosmetic Industry 59870-68-7
 
Glabridin Basic Info.:
 
Product name: Glabridin
CAS No.: 59870-68-7
Molecular Formula: C20H20O4
Molecular Weight: 324.37
Appearance: Light-yellow powder
Package: 5kg/drum, or at customer's requirements
Storage: Store in a cool, dry place and keep away from direct strong light.
Shelf Life: 2 years
 
Product Functions Of Glabridin:
 
Glabridin is a chemical compound that is found in the root extract of licorice (Glycyrrhiza glabra). It is used as an ingredient in cosmetics and is listed in International Nomenclature of Cosmetic Ingredients (INCI). Glabridin is a flavonoid molecule, this product is a larger family of plant-derived phenols.
 
Glabridin (glycyrrhiza glabra extract) in its main function as a potent, natural skin-whitening agent It is known for its beneficial effects on the skin due to its anti-inflammatory and antioxidant properties. In addition, glabridin inhibits melanogenesis. Some researchers have established that this effect may be due to the inhibition of tyrosinase activity. Glabridin whitens skin without being cytotoxic (destruction of pigment cells).
 

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Serilesine 1

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Sex Enhancement Medicine Avanafil For Treating Male Sexual Dysfunction 330784-47-9

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Sex Enhancement Medicine Avanafil For Treating Male Sexual Dysfunction 330784-47-9
 
Avanafil Basic Info:
 
Product Name: Avanafil
CAS: 330784-47-9
Molecular Formula: C23H26ClN7O3
Molecular Weight: 483.9506
Character: White to Off-White Cyrstalline Solid.
Assay: 99% min.
Store: Store at room temperature away from moisture, heat, and light.
Product Categories: Aromatics;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitor;Avanafil;Inhibitors
Usage: Used for the treatment of erectile dysfunction. A phosphodiesterase 5 inhibitor.
 
Avanafil Description:
 
Avanafil is a PDE5 inhibitor approved for erectile dysfunction by the FDA and EMA,it acts by inhibiting a specific phosphodiesterase type 5 enzyme which is found in various body tissues, but primarily in the corpus cavernosum penis and retina.Avanafil works the same way as the three other ED drugs currently on the market: Viagra, Cialis, and Levitra. All these drugs target an enzyme called PDE5,and avanafil appears to inhibit this enzyme more selectively than the other. It is absorbed quickly, reaching a maximum concentration in about 30-45 minutes. About two-thirds of the participants were able to engage in sexual activity within 15 minutes.Avanafil's most frequent side effect was headache, and the other common side effects included flushing and nasal congestion,this new drug may have fewer side effects.
 
Avanafil Application:
 
Avanafil is used to treat male sexual function problems such as impotence or erectile dysfunction,it is in a class of medications called phosphodiesterase inhibitors.Avanafil works by increasing blood flow to the penis to help a man get and keep an erection.This drug does not protect against sexually transmitted diseases such as HIV, gonorrhea and syphilis.To decrease your risk of infection, always use an effective barrier method during all sexual activity.
 

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Skin Lightening Hormone Peptide Nonapeptide-1 For Whitening 158563-45-2

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Skin Lightening Hormone Peptide Nonapeptide-1 For Whitening 158563-45-2
 
Nonapeptide-1 Basic Infor:
 
Product Name: Nonapeptide-1
Synonyms: Melanostatine-5;Nonapeptide-1;Melanostatine
CAS: 158563-45-2
MF: C61H87N15O9S
MW: 0
Product Categories: birth-giving pharm;Beauty peptide
 
Nonapeptide-1 Description:
 
Nonapeptide-1, also called Melanostatine 5, is a propriety peptide that was originally developed for its antimicrobial activities. Animal research has revealed, however, that nonapeptide-1 can inhibit the synthesis of melanin, which makes it of interest for treating certain skin conditions. Animal models suggest that nonapeptide-1 can reduce synthesis of melanin and help decrease skin pigmentation to a substantial degree.
 
Nonapeptide-1 is a skin lightening peptide, derived from the melanocyte stimulating hormone (MSH). It prevents the activity of tyrosine in the melanocytes, melanin synthesis inhibition and helps to even out your skin tone by lessening hyper-pigmentation. This process reduces the formation of unwanted pigmentation, allowing for the control over skin tone and brown spots.
 
Nonapeptide-1 Application:
 
Nonapeptide-1 is of primary research interest for its ability to reduce hyperpigmentation by inhibiting the action of tyrosinase in melanin-producing cells. The ability to regulate melanin production has potential application in a number of conditions, including photodamage of the skin.
 
Research also suggests that nonapeptide-1 may play a role in the central nervous system where it may act on both dopaminergic receptors and opioid receptors to modify pain signaling as well as behavior. Studies in mice support the idea that nonapeptide-1 may have central actions that affect behavior and pain.
 

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Somatostatin

Somatostatin is a 14-amino acid peptide. Somatostatin is produced by neuroendocrine neurons of the periventricular nucleus of the hypothalamus. It is also produced by several other populations that project centrally, and somatostatin receptors are expressed at many different sites in the brain. It regulates the endocrine system and affects neurotransmission and cell proliferation via interaction with G-protein-coupled somatostatin receptors and inhibition of the release of numerous secondary hormones. It is an inhibitor of growth hormone release from the anterior pituitary and hence an antagonist of GRF. Somatostatin suppresses the release of a variety of other hormones involved in the regulation of important physiological functions of the gastrointestinal tract. Somatostatin also inhibits TSH production.

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