Buy artificial human hormones | human hormones manufacturers | human hormones suppliers

chemical-categories

Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8
 
Trenbolone Enanthate Basic Info.
 
Product Name: Trenbolone Enanthate
Alias: Trenbolone Enanthate;Parabolan;Tren E;10161-33-8;Primobolan-depot;Primobolan-depot
CAS No.: 10161-33-8
Molecular Formula: C25H34O3
Molecular weight: 382.54
Assay: 99.02%
Appearance: pale yellow or yellow crystalline powder
Usage: Trenbolone Enanthate is only available from underground labs and was not designed for human consumption, although it is considered to be an ideal drug for bodybuilders who want to burn fat and gain muscle, although its long ester makes unwise for professional athletes who undergo testing to use.
 
Trenbolone Enanthate Description:
    
Trenbolone Enanthate also shines is in its ability to greatly preserve lean muscle tissue.When we diet, in-order to lose body fat, not weight but body fat we must be in a caloric deficit; we must burn more calories than we consume. As a result, as the body fights change with a desire to hang onto stored body fat due to its survival nature lean muscle tissue is often sacrificed in-order to meet its energy needs. As we lose more lean muscle tissue, this slows down the metabolic rate, and of course, it makes the physique look worse; Trenbolone Enanthate will prevent this. Of course, it gets even better; through its traits, Trenbolone Enanthate will provide the ultimate in visual conditioning effects.
 
Trenbolone Enanthate is a steroid that will greatly increase muscular endurance, more work can be done and you will not tire out as fast and it will also play an important role in recovery and healing.
 
Trenbolone Enanthate Applications:
 
Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.
 
Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds).
 

Properties Suppliers
Phenacetin Pharmaceutical Intermediates BP Grade Antipyretic Analgesic 62-44-2

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Phenacetin Pharmaceutical Intermediates BP Grade Antipyretic Analgesic 62-44-2
 
1. Phenacetin Quick Detail:
 
Product Name: Phenacetin
CAS: 62-44-2
EINECS Number: 200-533-0
Formula: C10H13NO2
MW: 179.2157
Density: 1.099g / cm3
Melting point: 133-138 °C
Boiling point: 355.1 °C at 760 mmHg
Flash Point: 168.5 °C
Water-soluble: 0.076 g / 100 mL
Vapor Pressure: 3.21E-05mmHg at 25 °C
Uses: Anti-inflammatory drugs
Assay: 99%
Appearance: White or almost white crystalline powder
 
2. Phenacetin Descriptions:
 
Phenacetin is a pain-relieving and fever-reducing drug, widely used from its introduction in 1887 until banned in the US by the FDA in 1983. Its use has declined because of its adverse effects, which include increased risk of certain cancers and kidney damage. It is metabolized into paracetamol, which replaced it in some over-the-counter medications following the ban on phenacetin.
 
3. Applications of Phenacetin:
 
Phenacetin was widely used until the third quarter of the twentieth century, often in the form of an "A.P.C." or aspirin-phenacetin-caffeine compound analgesic, as a remedy for fever and pain. An early formulation (1919) was Vincent's APC in Australia. However the U.S. Food and Drug Administration ordered the withdrawal of drugs containing phenacetin in November 1983, owing to its carcinogenic and kidney-damaging properties (Federal Register of October 5, 1983 (48 FR 45466)).
 
It was also banned in India.As a result some branded, previously phenacetin-based preparations continued to be sold, but with the phenacetin replaced by safer alternatives. A popular brand of phenacetin was Roche's Saridon, which was reformulated in 1983 to contain propyphenazone, paracetamol and caffeine. Coricidin was also reformulated without phenacetin. Paracetamol is a metabolite of phenacetin with similar analgesic and antipyretic effects, but the new formulation has not been found to have phenacetin's carcinogenicity.
 
Phenacetin is now being used as a cutting agent to adulterate cocaine in the UK and Canada, owing to the similar physical features of the two drugs.Due to low cost phenacetin is used for research into the physical and refractive properties of crystals. It is an ideal compound for this type of research.
 

Properties Suppliers
Phenethylamine

Phenethylamine is a natural monoamine alkaloid, trace amine, and psychoactive drug with stimulant effects. It is biosynthesized from the amino acid phenylalanine by enzymatic decarboxylation. Phenethylamine is an amine, consisting of a benzene ring and an aminoethyl group. Phenethylamine is a natural compound biosynthesized from the amino acid phenylalanine by enzymatic decarboxylation. It is also found in many foods such as chocolate. Phenethylamine releases norepinephrine and dopamine. Phenethylamine's half-life is 5-10 minutes. First attraction in humans causes to produce more phenethylamine which results in those dizzying feelings associated with romantic love. It increase both physical and emotional energy and at the same time releases more dopamine.

Properties Suppliers
Plant Extract Whitening Cosmetic Arbutin Arbutoside 497-76-7

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Plant Extract Whitening Cosmetic Arbutin Arbutoside 497-76-7
 
Arbutin Basic information
 
Product Name: Arbutin
Synonyms: 4-hydroxyphenyl-beta-d-glucopyranosid; Arbutin; Arbutoside
CAS: 497-76-7
MF: C12H16O7
MW: 272.25
EINECS: 207-850-3
Melting point: 195-198 °C
Alpha: -64 º (c=3)
Refractive index: -65.5 ° (C=4, H2O)
Storage temp.: 2-8°C
Solubility: H2O: 50 mg/mL hot, clear
Water Solubility: 10-15 g/100 mL at 20 ºC
Sensitive: Hygroscopic
Merck: 14,773
BRN : 89673
Stability: Stable. Hygroscopic - store under dry nitrogen.
Chemical Properties: Crystalline powder
Uses: Diuretic and anti-infective drugs of urinary system. Color photographic developing stabilizer. Whitening, anti-freckle, hair care in cosmetics.
Product Categories: Biochemistry;Glucose;Glycosides;Sugars;Natural Plant Extract;Herb extract;chemical reagent;pharmaceutical intermediate;phytochemical;standardized herbal extract;Uva, Ursi, p-Arbutin, Hydroquinone β-D-glucopyranoside;natural product;Inhibitors.
 
Product Description:
 
Alpha-Arbutin is a synthetic compound derived from natural plant sources. It is a water-soluble, white powder that remains stable in a pH range between 3.5 to 6.5. According to Lotion Crafters, a company offering skin care products, a 1 percent solution in clinical tests resulted in faster and better skin lightening after testing against other products for one month. Epidermal melanin biosynthesis, the effects of melanin on the skin, is blocked by Alpha-Arbutin; it reportedly works best when used for a period of two to three months.
 
Application:
 
1. Cosmetic industry:
Alpha Arbutin protect the skin against damage caused by free radicals Alpha Arbutin is a skin whitening agent which is very popular in Japan and Asian countries for skin de-pigmentation, Alpha Arbutin inhibits the formation of melanin pigment by inhibiting Tyrosinase activity. Alpha Arbutin is very safe skin agent for external use which does not have toxicity, stimulation, unpleasant odor or side effect such as Hydroqinone.The encapsulation of Alpha Arbutin constitute a delivery system to potentialize the effect in time.
 
2. Medical industry:
Back in the 18th century, Alpha Arbutin was first used in medical areas as an anti-inflammatory and antibacterial agent. Alpha Arbutin was used particularly for cystitis, urethritis and pyelitis. These uses still until today where natural medicine uses only natural ingredients to treat any disease. Also Alpha Arbutin may be used to repress the virulence of bacterial pathogens and to prevent contaminating bacteria, Alpha Arbutin is also used for treating allergic inflammation of the skin.
 
Function :
 
1.Alpha arbutin will relieve and dispell chloasma, melanin, acne ect;
2. Alpha arbutin has good effects of sterilization and relieving cough;
3. It used to alleviate pain of burn and scald,enhancing immune fuction;
4.It can promote skin elasticity, retaining skin moisture and slowing down aging skin;
5.It has function of restraining the activity of tyrosinase; preventing the formation of melanin.
 

Properties Suppliers
Polypeptide Hormone Follistatin 315 Antibody Fst-315

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Polypeptide Hormone Follistatin 315 Antibody Fst-315
 
Follistatin 315 Basic Info.
 
Product Name: Follistatin 315 / Fst-315
Specification: 1mg/vial
Purity: 85%+
Appearance: White powder
Specific Optical Rotation (c=0.5,10% HAc): -50.0~-60.0°
Water Content(Karl Fischer): ≤5.0%
Acetate Content(by HPLC): ≤15.0%
Amino Acid Composition: ±10% of theoretical
Purity (by HPLC): ≥98.0%
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
Storage/Stability: Stored at -20 °C if preferred. Storage in frost-free freezers is not recommended.
Note: This product is furnished for LABORATORY RESEARCH USE ONLY. Not for diagnostic or therapeutic use.
 
Description of Follistatin 315:
 
Follistatin is being studied for its role in regulation of muscle growth in mice, as an antagonist to myostatin (also known as GDF-8, a TGF superfamily member) which inhibits excessive muscle growth. Lee & McPherron demonstrated that inhibition of GDF-8, either by genetic elimination (knockout mice) or by increasing the amount of follistatin, resulted in greatly increased muscle mass.In 2009, research with macaque monkeys demonstrated that regulating follistatin via gene therapy also resulted in muscle growth and increases in strength. This research paves the way for human clinical trials, which are hoped to begin in the summer of 2010 on Inclusion body myositis.
A study has also shown that increased levels of follistatin, by leading to increased muscle mass of certain core muscular groups, can increase life expectancy in cases of spinal muscular atrophy (SMA) in animal models.
It is also being investigated for its involvement in polycystic ovary syndrome (PCOS), though there is debate as to its direct role in this infertility disease.
 
Follistatin 315 Application:
 
Follistatin 315 primary function is the binding and bioneutralization of members of the TGF-β superfamily, with a particular focus on activin, a paracrine hormone.
 
Storage Instruction
Store at +4°C or at -20°C if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
 

Properties Suppliers
Polypeptide Human Growth Powder Hormone Peptide Selank CAS 129954-34-3

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Polypeptide Human Growth Powder Hormone Peptide Selank CAS 129954-34-3
 
Selank Basic Info.
 
Product Name: Selank
Alias: Selanc;Selank
Sequence: Thr-Lys-PRO-Arg-PRO-Gly-PRO
CAS: 129954-34-3
MF: C33H57N11O9
MW: 751.9
Purity: 99%
Specification: 5mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Use: Reduce stress, relieve depression, insomnia quit. Of course, with Selank a puzzle-anxiolytic
 
Descriptions Of Selank:
 
Selank was developed by the Russian Academy of Sciences. anxiolytic peptide based drugs. Selank is a heptapeptide with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. It is a synthetic analogue of a human tetrapeptide tuftsin.
 
it uses relief of anxiety and improved cognitive functioning alone. Selank used for : Stress reduction, the alleviation of depression, reversal of anhedonia, improvement in mood in emotionally stable individuals, and cessation of insomnia.
 
In fact,Selank more suitable for long-term use. for the large majority of researchers claiming that it is a "side effect free" compound. Some believe an overdose might cause fatigue.
 
Application Of Selank:
 
(1)Selank as a nootropic:
Recreationally Selank is used to improve one's ability to focus and concentrate, reduce mental fatigue, increase mental sharpness and increase memory and learning capacity. The first noticeable effect is usually stabilization of mood and general feeling of well-being.
 
(2)Selank as an antiviral agent:
Selank neuropeptide also expresses immunomodulatory effects. In 2009 a study by F. Ershov et all. has evaluated antiviral properties of Selank both in vitro and in vivo against the influenza virus strain A/Aichi 2/68 (H3N2). The pronounced antiviral effect of Selank was detected in both systems. The highest efficiency - completely supressed viral reproduction was shown when Selank was added to the cell culture 24 hours before inoculation.
 

Properties Suppliers
Progesterone

Progesterone is a C-21 steroid hormone involved in the female menstrual cycle, pregnancy and embryogenesis of humans and other species. Progesterone belongs to a class of hormones called progestogens, and is the major naturally occurring human progestogen.Progesterone is commonly manufactured from the yam family, Dioscorea.It is synthesized from pregnenolone.It can be synthesized within the central nervous system and also serves as a precursor to another major neurosteroid, allopregnanolone.Progesterone has a number of physiological effects that are amplified in the presence of estrogen.It aids in immunity, reduces swelling and inflammation, stimulates and regulates the production of the thyroid gland, and keeps blood-clotting levels at normal values. Progesterone also can be said to be an anti-aging hormone. It keeps bones strong, produces collagen, and helps keep nerves functioning at appropriate levels. Progesterone has key effects via non-genomic signalling on human sperm as they migrate through the female tract before fertilization occurs.Progesterone modulates the activity of CatSper (cation channels of sperm) voltage-gated Ca2+ channels.Progesterone converts the endometrium to its secretory stage to prepare the uterus for implantation.Progesterone is used to support pregnancy in Assisted Reproductive Technology cycles such as In-vitro Fertilization,used to control persistent anovulatory bleeding. It is also used to prepare uterine lining in infertility therapy and to support early pregnancy.

Properties Suppliers
Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3 
 
Gestodene Basic Info.:
 
Product name: Gestodene
Other names: Gestinol;13-Ethyl-17-hydroxy-18,19-dinor-17alpha-pregna-4,15-dien-20-yn-3-one;SHB 331;Gestodeno.
CAS: 60282-87-3
EINECS: 262-145-8
Molecular Formula: C21H26O2
Molecular Weight: 310.43
Melting point: 190-192 degree centigrade
Boiling Point: 462.7 degree centigrade at 760 mmHg
Flash Point: 196.9 degree centigrade
Refractive index:1.588
Density: 1.15 g/cm3
Vapour pressure: 1.66E-10mmHg at 25 degree centigrade
Appearance: White crystalline solid. 
Function: Used as resisting pregnant hormone pills.
 
Gestodene Description:
 
Gestodene is a synthetic version of a female sex hormone. When combined with other synthetic hormones, it interferes with a woman's menstrual cycle, decreasing the symptoms of severe menstruation and preventing pregnancy. Used correctly, it is more than 99% effective at preventing unwanted pregnancies.
 
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect. Oral absorption quickly and completely, after 1 to 2 hours of peak blood concentration, bioavailability 100%, eliminating t1 / 28 hours. Clinical and ethinyl estradiol or a composite sheet consisting of three photo used for short-acting oral contraceptives. Due to its reliable contraceptive effect, good cycle control, on lipid metabolism can produce beneficial effects, improve hdl, it is the most ideal one oral contraceptives.
 
Gestodene Applications:
 
Gestodene is asoral contraceptive. It mimics the naturally occurring female sex hormone progesterone, 
which is partially responsible for regulating the menstrual cycle. 
 
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect.
 

Properties Suppliers
Prohormones Steroids White Powder Misoprostol For Terminate Pregnancy 59122-46-2

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Prohormones Steroids White Powder Misoprostol For Terminate Pregnancy 59122-46-2
 
Misoprostol Basic Info.
 
Product Name: Misoprostol
Synonyms: Misoprostol;Cytotec;SC-29333
CAS: 59122-46-2
Molecular Formula: C22H38O5
Molecular Weight: 382.60
Assay: 99%
Chemical Properties: White Solid
Solubility: Soluble to 100 mM in Ethanol
Safety: Poison by ingestion, intramuscular, and intraperitoneal routes. When heated to decomposition it emits acrid smoke and irritating fumes.
Package: Aluminium foil bag packing 
Storage: Keep in cool and dry place, away from light
 
Misoprostol Description:
 
Misoprostol is a medication used to start labor, induce abortions, prevent and treat stomach ulcers, and treat postpartum bleeding due to insufficient contraction of the uterus. For abortions it is used with mifepristone or methotrexate. It is a synthetic prostaglandin E1 (PGE1).
 
Common side effects include diarrhea and abdominal pain. It is pregnancy category X meaning that it is known to result in negative fetal outcomes if taken during pregnancy. Uterine rupture may occur.
 
It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system. Misoprostol was invented and marketed by G.D. Searle & Company under the trade name Cytotec, but other trade names and generic formulations are available.
 
Misoprostol Usage
 
Misoprostol is approved for use in the prevention of NSAID-induced gastric ulcers. It acts upon gastric parietal cells, inhibiting the secretion of gastric acid by G-protein coupled receptor-mediated inhibition of adenylate cyclase, which leads to decreased intracellular cyclic AMP levels and decreased proton pump activity at the apical surface of the parietal cell. Because other classes of drugs, especially H2-receptor antagonists and proton pump inhibitors, are more effective for the treatment of acute peptic ulcers, misoprostol is only indicated for use by people who are both taking NSAIDs and are at high risk for NSAID-induced ulcers, including the elderly and people with ulcer complications. Misoprostol is sometimes coprescribed with NSAIDs to prevent their common adverse effect of gastric ulceration (e.g. with diclofenac in Arthrotec).
 
Misoprostol has other protective actions, but is only clinically effective at doses high enough to reduce gastric acid secretion. For instance, at lower doses, misoprostol may stimulate increased secretion of the protective mucus that lines the gastrointestinal tract and increase mucosal blood flow, thereby increasing mucosal integrity. However, these effects are not pronounced enough to warrant prescription of misoprostol at doses lower than those needed to achieve gastric acid suppression.
However, even in the treatment of NSAID-induced ulcers, omeprazole proved to be at least as effective as misoprostol,but was significantly better tolerated, so misoprostol should not be considered a first-line treatment. Misoprostol-induced diarrhea and the need for multiple daily doses (typically four) are the main issues impairing compliance with therapy.
 
The most commonly reported adverse effect of taking a misoprostol orally for the prevention of stomach ulcers is diarrhea. In clinical trials, an average 13% of patients reported diarrhea, which was dose-related and usually developed early in the course of therapy (after 13 days) and was usually self-limiting (often resolving within 8 days), but sometimes (in 2% of patients) required discontinuation of misoprostol.
 
The next most commonly reported adverse effects of taking misoprostol orally for the prevention of gastric ulcers are: abdominal pain, nausea, flatulence, headache, dyspepsia, vomiting, and constipation, but none of these adverse effects occurred significantly more often than when taking placebos. In practice, fever is almost universal when multiple doses are given every 4 to 6 hours.
 
Misoprostol should not be taken by pregnant women to reduce the risk of NSAID-induced gastric ulcers because it increases uterine tone and contractions in pregnancy, which may cause partial or complete abortions, and because its use in pregnancy has been associated with birth defects.
 

Properties Suppliers
Prostacyclin

Prostacyclin is a member of the family of lipid molecules known as eicosanoids. Prostacyclin is produced in endothelial cells from prostaglandin H2 by the action of the enzyme prostacyclin synthase. Prostacyclin chiefly prevents formation of the platelet plug involved in primary hemostasis. It does this by inhibiting platelet activation. It is also an effective vasodilator. Prostacyclin has a half-life of 42 seconds, is broken down into 6-keto-PGF1. It is released by healthy endothelial cells and performs its function through a paracrine signaling cascade that involves G protein-coupled receptors on nearby platelets and endothelial cells .It unifies and strengthens contractions during pregnancy and decreases tumor growth in some forms of cancer. It also appears to exert a protective action against allergic inflammation by decreasing the ability of inflammatory white blood cells to attach and move between the endothelial tissue lining blood vessels. Prostacyclin is not stored, instead it is created on-demand by endothelial cells that line blood vessels.

Properties Suppliers