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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5

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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5
 
Androstenediol Basic information:
 
Product Name: Androstenediol
Synonyms: Hermaphrodiol;5-Androstenediol;Androstenediol
CAS: 521-17-5
MF: C19H30O2
MW: 290.44
EINECS: 208-306-8
Product Categories: Steroids;API
Melting point: 178-182°C
Alpha: -52.2 º (c=0.4,2-propanol)
Storage temp.: 2-8°C
 
Androstenediol Description:
 
Androstenediol, commonly referred to simply as , and also known as androst-5-ene-3β,17β-diol, is an endogenous androgen and estrogen steroid hormone and intermediate in the biosynthesis of testosteronefrom dehydroepiandrosterone.
Androstenediol is a direct metabolite of the most abundant steroid produced by the human adrenal cortex. It is less androgenicthan the related compound, Δ4-androstenediol, and has been found to stimulate the immune system. When administered to rats, Δ5-diol, in vivo, has approximately 1.4% of the androgenicity , 0.54% of the androgenicity of androstenedione, and 0.21% of the androgenicity of testosterone.
 
1.People Use Androstenediol For:
 Orally, 5-Androstenediol is used to increase endogenous testosterone production to increase energy, enhance recovery and growth from exercise, heighten sexual arousal and function, and to promote a greater sense of well being.
 
2.Mechanism of Action:  
5-Androstenediol, a prohormone, is a weak steroid hormone and is a direct precursor of testosterone . Androstenediol can be converted to estradiol, estrone, dehydroepiandrosterone (DHEA), and testosterone; and may increase levels of these hormones. 
 

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Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8

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Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8
 
Epiandrosterone Basic Info.:
 
Product Name: Epiandrosterone
Synonyms: Trans-Androsterone;3beta-Androsterone;3-Epiandrosterone;3-Hydroxyandrostan-17-one;
CAS No.: 481-29-8
MF: C19H30O2
MW: 290.44
EINECS: 207-563-3
Purity: ≥ 99%
Melting point: 172-174 °C
Loss on drying: 0.23%
Alpha: 91°(c=1, CH3OH)
Storage temp.: Refrigerator
Water Solubility: practically insoluble
Appearance: White to off-white crystalline powder
Packaged by: 25kg/drum
Product Categories: Pharmaceutical Intermediates;Steroids;17-Ketosteroids;Biochemistry;Hydroxyketosteroids;Intermediates & Fine Chemicals;Pharmaceuticals;API;Inhibitors
Usage: For the steroid hormone drugs.
 
Epiandrosterone Description:
 
Epiandrosterone, or 3β-androsterone, also known as 3β-hydroxy-5α-androstan-17-one or 5α-androstan-3β-ol-17-one, is a steroid hormone with weak androgenic activity. It is a natural metabolite of dehydroepiandrosterone (DHEA) via the 5α-reductase enzyme. It was first isolated in 1931, by Adolf Friedrich Johann Butenandt and Kurt Tscherning.
 
They distilled over 17,000 litres of male urine, from which they got 50 milligrams of crystalline androsterone (most likely mixed isomers), which was sufficient to find that the chemical formula was very similar to estrone.
 
Epiandrosterone Applications:
 
Typical dosage is in the range of 300-400 mg/day, though some users may dose higher than this. This is best used in 4-6 week cycles. Although Epiandrosterone does not cause severe shut down of testosterone production like many other prohormones, it is still a good idea too use a mild over the counter post-cycle therapy. An over the counter anti-estrogen/test booster will do just fine for recovery from an epiandrosterone cycle.
 
As mentioned earlier, epiandrosterone and its 3-alpha isomer androsterone are completely legal and available over the counter. LG Sciences MMv3 uses the 3-alpha isomer of this compound because it is better for the special sublingual delivery system that this product utilizes. By placing a tablet under the tongue, the compound is absorbed directly through the tissues in that area and into the blood stream.
 

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9
 
Clomiphene Citrate Basic Info.:
 
Product Name: Clomiphene Citrate
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene.
 
Clomiphene Citrate Description:
 
Clomiphene Citrateis a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, putsClomiphene Citratein a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. As for women, the only real use for Clomiphene Citrate is the possible management of endogenous estrogen levels near contest time. This can increase fat loss and muscularity, particularly in female trouble areas such as this HIPS and thighs. Clomiphene Citrate however often produces troubling side effects in women (discussed below), and is likewise not in very high demand among this group of athletes. Clomid are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time.
 
Clomiphene Citrate Application:
 
As for toxicity and side effects, Clomiphene Citrateis considered a very safe drug. Bodybuilders seldom report any problems, but listed possible side effects do include hot flashes, nausea, dizziness, headaches and temporarily blurred vision. Clomifene citrate is a drug treatment that stimulates your ovaries to release eggs. Ovulation stimulation using clomifene citrate is a well-established, effective treatment. Clomifene citrate is the most widely used of all fertility drugs. Other drugs that may be used to treat ovulation disorders include metformin and bromocriptin.
 

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Human Chorionic Gonadotropin

Human Chorionic Gonadotropin is a glycoprotein hormone produced during pregnancy that is made by the developing embryo after conception and later by the syncytiotrophoblast.It is a glycoprotein composed of 244 amino acids.It is heterodimeric, with an α (alpha) subunit identical to that of luteinizing hormone (LH), follicle-stimulating hormone (FSH), thyroid-stimulating hormone (TSH), and β (beta) sub unit.It interacts with the LHCG receptor and promotes the maintenance of the corpus luteum during the beginning of pregnancy, causing it to secrete the hormone progesterone.Human chorionic gonadotropin can be used as a tumor marker, as its β subunit is secreted by some cancers including seminoma, choriocarcinoma, germ cell tumors, hydatidiform mole formation, teratoma with elements of choriocarcinoma, and islet cell tumor.It is extensively used parenterally as an ovulation inducer in lieu of luteinizing hormone.

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Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin 33515-09-2

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Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin 33515-09-2
 
Gonadorelin Basic Info.:
 
Product Name: Gonadorelin
Other Name: LH-RH, human, Gonadoreline
CAS: 33515-09-2
Purity (HPLC): 98.0%min.
Appearance: White powder
Molecular Formula: C59H83N17O17
Molecular Weight: 1302.39
Single Impurity (HPLC): 0.5%max
Amino Acid Composition: ±10% of theoretical
Peptide Content (N%): ≥80.0% 
Water Content(Karl Fischer): ≤8.0%
Acetate Content(HPIC): ≤10.0%
Specific Rotation (20/D): -55.0~-65.0°(c=1 1%HAc)
MS (ESI): Consistent
Mass Balance: 95.0~105.0%
 
Gonadorelin Description:
 
Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.
GnRH is available as gonadorelin hydrochloride(Factrel®)and gonadorelin diacetate tetrahydrate(Cystorelin®)for injectable use. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. It is also used in veterinary medicine as a treatment for cattle with cystic ovarian disease.
 
Gonadorelin Application:
 
Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use.
 

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Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin Acetate 71447-49-9

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Human Growth Peptides IGF-1 IGF1 Human Des1-3

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Human Growth Peptides IGF-1 IGF1 Human Des1-3
 
IGF-1 Basic Info.
 
Product Name: IGF1 Human Des1-3 (IGF-1)
Molar Mass: 7,372 Da
Synonyms: IGF-1Des(1-3); Des1-3; Des 1-3; Des (1-3)
Compound: Thr-Leu-Cys-Gly-Ala.
Purity: 99.21%
 
IGF-1 IGF-1DES Dose:
 
DES IGF-1 can be dosed at 50-150mcg multiple times a day (prior to training) into specific target areas. since DES has such a short half life (20-30 minutes), desensitization was not noticed at all . Injection sites should be localized; preferably, at the muscle group you want to grow. In simple terms, if you want to grow your biceps, inject IGF-1DES right into your bicep.
 
IGF-1 IGF-1DES Half-life:
 
DES IGF-1 is the shorter version of the IGF-1 chain. It is five (5) times more powerful than IGF-1LR3 and ten (10) times more powerful than regular base IGF-1. The half-life for DES is about 20-30 minutes, which means this is a very delicate chain. Therefore, administration should only be done at the site where you want to see muscle growth. DES has the ability to stimulate muscle hyperplasia better than LR3. In simple terms, it's best used for site injections, rather than overall growth.
In addition, DES is known to bind to receptors that have been deformed by lactic acid, which is often present during workouts. This allows the DES to attach itself to a mutated receptor and signal tissue growth during training. DES can be used longer and more frequently than LR3.
 

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Human Growth SR9009 Powder SR-9009 1379686-30-2

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Human Growth SR9009 Powder SR-9009 1379686-30-2
 
SR 9009 Basic Info.
 
Product Name: SR 9009
SR9009 Prohormone Steroids SARMS
CAS: 1379686-30-2
MF: C20H24ClN3O4S
MW: 437.94
Purity: 99%
Appearance: White powder
Solubility: DMSO
Application: SR9009 increase exercise endurance and loss weight.
 
SR 9009 Description:
 
SR9009 also known as Stenabolic,is a synthetic Rev-Erb ligand and PPAR alpha modifier drug,which is taken orally.This is a very unique compound. By stimulating the Rev-Erb protein, SR9009 has the ability to greatly influence a lot of regulatory mechanisms in the human body.it can affect the circadian rhythms, lipid and glucose metabolism, fat-storing cells, as well as macrophages. SR9009 will allow the user to lose fat and drastically increase endurance, both of which are very desirable effects for an athlete.
 
How SR 9009 Works?
 
By binding and activating the Rev-Erb protein, Stenabolic triggers a very wide range of processes in the body. The most prominent being the increase of mitochondria count in the muscles and an enhanced metabolism.That causes a drastic improvement in endurance and muscle strength.And thanks to the increase in number of macrophages, defective mitochondria are removed from the muscles and replaced with new ones.
 
Furthermore, the change in metabolic rates increases energy expenditure by 5% even when the user is resting.It burns excess calories and doesn’t allow them to convert into fat.Coupled with enhanced metabolism of glucose, helps effectively burn fat, which makes the body act is if it were in a constant state of exercise.
 
This means that less fat is stored, less cholesterol is developed by the liver, and more fat and glucose is burned in the muscles.
 

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Human Placental Lactogen

Human Placental Lactogen is a polypeptide placental hormone.It is originate in the syncytiotrophoblasts.Its structure and function is similar to that of human growth hormone. It modifies the metabolic state of the mother during pregnancy to facilitate the energy supply of the fetus.It has anti-insulin properties.It affects the metabolic system of the maternal organism.Human Placental Lactogen decreases maternal insulin sensitivity, and, therefore, raises maternal blood glucose levels, whilst decreasing maternal glucose utilization, which helps ensure adequate fetal nutrition.

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Hydrocortisone

Hydrocortisone is a steroid hormone, or glucocorticoid, produced by the adrenal gland. It is released in response to stress and a low level of blood glucocorticoids. Its primary functions are to increase blood sugar through gluconeogenesis, suppress the immune system, and aid in fat, protein and carbohydrate metabolism.Hydrocortisone counteracts insulin, contributes to hyperglycemia-causing hepatic gluconeogenesis and inhibits the peripheral utilization of glucose (insulin resistance) by decreasing the translocation of glucose transporters (especially GLUT4) to the cell membrane,stimulates gastric-acid secretion.It acts as a diuretic hormone, controlling one-half of intestinal diuresis.It reduces bone formation, favoring long-term development of osteoporosis. It transports potassium out of cells in exchange for an equal number of sodium ions,increases blood pressure by increasing the sensitivity of the vasculature to epinephrine and norepinephrine,inhibits secretion of corticotropin-releasing hormone.

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