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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building

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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building
 
Androstenedione Basic Info.
 
Product Name: Androstenedione
Synonyms: 4-Androstenedione;4AD;3,17-Dioxoandrost-4-Ene;delta-(sup4)-Androsten-3,17-dione;delta(Sup4)-Androstene-3,17-dione;delta4-androsten-3,17-dione;delta-4-androstenedione;SKF 2170;skf2170;4-AD
CAS: 63-05-8
MF: C19H26O2
MW: 286.41
EINECS: 200-554-5
Purity: 98.88%
Manufacturer: Kafen
Characters: Near white crystalline powder, soluble in ethanol, insoluble in water
 
Androstenedione Applications:
 
Testo-ster-one precursor and metabolite with androgenic activity. Controlled substance (anabolic steroid); Simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.
 
Androstenedione Description:
 
4-Androstenedione can be synthesized in one of two ways. The primary pathway involves conversion of 17-hydroxypregnenolone to dehydroepiandrosterone by way of 17,20-lyase, with subsequent conversion of dehydroepiandrosterone to 4-Androstenedione via the enzyme 3-β-hydroxysteroid dehydrogenase. The secondary pathway involves conversion of 17-hydroxyprogesterone, most often a precursor to cortisol, to 4-androstenedione directly by way of 17,20-lyase. Thus, 17,20-lyase is required for the synthesis of 4-androstenedione, whether immediately or one step removed.  
 
The production of adrenal 4-Androstenedione is governed by ACTH, whereas production of gonadal 4-Androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total 4-androstenedione(about 3 mg/day). After menopause, 4-androstenedione production is about halved, due primarily to the reduction of the steroid secreted by the ovary. Nevertheless, 4-androstenedione is the principal steroid produced by the postmenopausal.
 

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Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

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Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

Stanozolol Basic Info.

Product Name: Stanozolol (Stanazol)

Alias: Winstrol;Stromba;Stanozolol;Winny Depot;Stanazol.

CAS No: 10418-03-8

MF: C21H32N2O

MW: 328.49

Einecs No: 233-894-8

Purity: 99%

MOQ(minimum order quantity):10gram

Standard: Enterprise Standard

Appearance: White crystalline powder.

Usage: Stanazol Winstrol is the trade name for the anabolic steroid Stanazol. This is the third most popular and widely used anabolic steroid in all history and in the whole world;And is a very commonly used anabolic steroid for cutting cycles.

Stanozolol Description:

Winstrol - Stanazol  is a very commonly used anabolic steroid for cutting cycles. While many people will attempt to use Dianabol or even Anadrol for cutting cycles, Ive really never heard of anyone using Stanazol  for anything except a cutting cycle. Its a bit of a one-trick-pony in this respect. Let me repeat that: Stanazol  is a cutting drug. Not many people will argue for its use in a bulking cycle. Its certainly not a very effective compound for treating anemia (1) and thus, one could rightly assume that its role in bulking cycles is very limited. One novel use for Winstrol in any cycle (perhaps even bulking) would be to use it at a very limited dose, in order to lower SHBG. (2) One of the properties of Winstrol is its profound ability to lower SHBG much more than other steroids. A dose of .2mg/kg lowered SHBG significantly, which would in turn, raise the amount of free testosterone circulating in the body. As with 99% of steroids, however, its important to note that suppression of your natural hormonal levels will occur (though perhaps not to the extent that it will with many other steroids).(10) As with running virtually any compound, testosterone supplementation (i.e. running test in a cycle containing Winstrol) is warranted to avoid possible sexual dysfunction.

Stanozolol Applications:

Winstrol is the trade name for the anabolic steroid Stanazol . This is the third most popular and widely used anabolic steroid in all history and in the whole world. The first most popular anabolic steroid is Dianabol (Methandrostenolone), second most popular is Nandrolone Decanoate (Deca Durabolin), and the third most popular is Stanazol  In particular, Winstrol is the anabolic steroid best known for its supposed use by Canadian Olympic sprinter Ben Johnson when he was tested positive for this compound in the 1988 Seoul Summer Olympic Games. Winstrol's information was first documented, published, and released in 1959. Shortly thereafter, Winthrop Laboratories located in the United Kingdom manufactured it into a prescription drug for use, and in 1961 Sterling in the United States purchased the patent for the drug. Shortly thereafter, it was then released onto the North American market and given the brand name label of Winstrol.

 

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Male Hormone Fitness Anabolic Steroids Powder Nandrolone Undecylate / Dynabolon 862-89-5

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Male Hormone Fitness Anabolic Steroids Powder Nandrolone Undecylate / Dynabolon 862-89-5
 
Nandrolone Undecylate Basic Info.:
 
Product Name: Nandrolone Undecylate
Synonyms: Nandrolone Undecanoate; Nandrolone 17β-Undecanoate;Dynabolon
CAS: 862-89-5
MF: C29H46O3
MW: 442.68
EIENCS: 212-729-3
Assay: 99% min.
Packing: foil bag or tin.
Delivery: Express courier.
Usage: pharmaceutical material, Tibolone intermediate.
Standard: Enterprise standard
 
Nandrolone Undecylate Description: 
 
Nandrolone undecylate is an effective compound that produces quality, long-lasting muscle gains. This is because of the relatively long half-life of the drug (around 8 days). Users report mild side effects, with the biggest side effect being water retention. 
 
Nandrolone Undecylate Applications:
 
Nandrolone is most commonly found with a cypionate, laurate, decanoate or plenylpropionate ester. Briefly explained, the ester determines how much of the given hormone is released over a period of time. Longer esters such as decanoate peak slowly and can keep stable blood plasma levels up to ten days, shorter esters such as the phenylpropionate peak more rapidly but the half-live is shorter. Shorter esters usually release much more active hormone per mg than longer esters, and of course, allow the drugs effects to leave your system more quickly.
 

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Male Sex Hormone Androsta-3, 5-Diene-7, 17-Dione / Arimistane Powder Cortisol Inhibitor 1420-49-1

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Male Sex Hormone Androsta-3, 5-Diene-7, 17-Dione / Arimistane Powder Cortisol Inhibitor 1420-49-1
 
Androsta-3,5-Diene-7,17-Dione Basic Info.:
 
Product Name: Androsta-3,5-diene-7,17-dione
Synonyms: 3,5-Androstadiene-7,17-dione;Androsta-3,5-diene-7,17-dione;Androst-3,5-diene-7,17-dione;NSC 134910;Androst-3,5-dien-7,17-dione;Arimistane
CAS: 1420-49-1
MF: C19H24O2
MW: 0
Melting point: 167-168℃
Appearance: Pale yellow crystalline powder
 
Androsta-3, 5-Diene-7, 17-Dione Arimistane Profile:
 
Arimistane (Androsta-3,5-diene-7,17-dione) is a metabolite of 7-Keto DHEA, which does not convert into testosterone or estrogen. In fact, just like the drug Aromasin, arimistane is actually a suicide aromatase inhibitor (AI), so it will permanently bind to the aromatase enzyme and prevent any estrogen rebound. Furthermore, it has also been shown to reduce cortisol, raise LH (luteinizing hormone), and increase testosterone levels.
 
How Do You Use Androsta-3, 5-diene-7, 17-dione?
 
Before taking Androsta-3, 5-diene-7, 17-dione, make it a point to check with your doctor and discuss your medical condition and the possible side effects. People who are suffering from diabetes, psychiatric disease, heart disease, and liver and kidney problems must follow the prescribed dosage and medical guidelines to make sure that the supplement would not set off any adverse effects sooner or later.
 
The Recommended Dosage to Use:
 
The right amount of Androsta-3, 5-diene-7, 17-dione to be taken for first time users is 30 mg daily. Taking this AI in larger quantities may cause discomfort and other side effects such as muscle pain, vaginal dryness, and hot flashes. If you experience some side effects, call your doctor immediately.
 

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Manufacturer Terlipressin Acetate With High Quality 14636-12-5

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Manufacturer Terlipressin Acetate With High Quality 14636-12-5
 
Terlipressin Acetate Basic Info.:
 
Product Name: Terlipressin Acetate
Synonyms: Terlipressin;Terlipressin Acetate;Terilipressin;
CAS: 14636-12-5
MF: C52H74N16O15S2
MW: 1227.37
EINECS: 238-680-8
Product Categories: Amino Acid Derivatives;Peptide;hormones
Usage: Terlipressin is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. Terlipressin is used norepinephrine-resistant septic shock and hepatorenal syndrome. Terlipressin is also used in the treatment of acute variceal bleeding.
 
Terlipressin Acetate Pharmacological Effects:
 
Terlipressin is a novel long-acting synthetic vasopressin reagent,its chemical name is three glycyl lysine vasopressin, it is a prodrug, itself has no activity ,in vivo  , it removes three glycyl residues in its N-terminus by aminopeptidase, and slowly "releases" the active lysine vasopressin. It is this "slow release" mechanism that makes it maintain the smooth muscle contraction up to 10 hours after a single administration, whereas the same dose of vasopressin, it can maintain its activity for 20-40 minutes. On the other hand,because of the slow digestion,  lysine vasopressin in the circulation cannot reach toxic levels, and usage of  terlipressin is safer.
Pharmacological effect of terlipressin is splanchnic vascular smooth muscle contraction, and reduction of visceral blood flow (such as reducing blood flow in the mesentery, spleen, uterus, etc.), thereby reducing portal vein blood flow,and reducing portal pressure, on the other hand it may also reduce plasma renin concentration, thereby increasing the renal blood flow in patients with hepatorenal syndrome, to improve kidney function, and increase urine output. Terlipressin is currently the only drug which is able to increase mortality in patients with esophageal varices bleeding , it is previously mainly used in clinical for the treatment of variceal bleeding, in addition,terlipressin now has also been successfully used for liver and kidney integrated syndrome and refractory shock, it is also likely to play a useful role in the cardiopulmonary resuscitation . Compared with vasopressin, it has a lasting effect, and it does not cause dangerous complications, including promoting  fibrinolysis and severe complications in the cardiovascular systems, and the use of it is simple (available intravenous injection), it is more suitable for rescue and treatment of emergent and critical  patients.
 
Terlipressin Acetate Mechanism of Action:
 
Terlipressin, a synthetic triglycyl-lysine derivative of vasopressin, is a inactive prodrug. It has pressor and antidiuretic effects. Following IV injection, lysine vasopressin are released following the enzymatic cleavage of 3 glycyl moieties.
Duration: 4-6 hr.
 

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Masteron

CAS: 521-12-0 MF: C23H36O3 MW: 360.53 EINECS: 208-303-1 Assay: 99% min. Usage: can be used as pharmaceutical material. Its main function is to promote metabolism. Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation. Tel:00862781331422 Fax:00862781685200 Cel:+8615337164625 Skype:leslie(at)carphetin(dot)com Email:leslie(at)carphetin(dot)com

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Masteron Raw Steroid Powder Drostanolone Propionate For Muscle Building 521-12-0

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Masteron Raw Steroid Powder Drostanolone Propionate For Muscle Building 521-12-0
 
Drostanolone Propionate Basic Info.
 
Product Name: Drostanolone Propionate 
Synonyms: Masteron; Dromostanolone Propionate 
CAS: 521-12-0 
Molecular formula: C23H36O3 
Molecular weight: 360.53 
EINECS: 208-303-1 
Assay: 99%
Packing: Foil bag or tin. 
Delivery: Express courier. 
Character: White crystalline powder. 
Min. order quantity: 100g
Payment: T/T, Western Union, Moneygram
Express: EMS, DHL, FeDex, etc(door-to-door)
Delivery : safe & timely, within 12 hours after payment
 
Drostanolone Propionate Description:
 
Masteron can be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass. It can also be successfully combined with other steroids for an enhanced effect. Mixing drostanolone with an injectable anabolic such as Deca-Durabolin or Equipoise can prove quite useful for example, the two providing notably enhanced muscle gain without excessive water retention. For greater mass gains, a stronger androgen such as Dianabol or an injectable testosterone would do the trick. The result here can be an extreme muscle gain, with a lower level of water retention & other estrogenic side effects than if these steroids were used alone (usually in higher doses). Masteron could of course be used during cutting phases of training as well. A cycle of this drug combined with Winstrol, Primobolan or Oxandrolone should provide great muscle retention and fat loss, during a period which can be very catabolic without steroids. It is an added benefit that none of these steroids aromatize, and therefore there is no additional worry of unwanted water and fat retention.
 
Drostanolone Propionate Applications:
 
Bodybuilders have a strong like for non-aromatizing androgens, and find Masteron very useful in a cutting phase. It is generally used for a number of weeks prior to a competition, in an effort to bring out an improved look of density and hardness to the muscles. As long as body fat percentage is low enough, considerably intensifies its anabolic effect. It can therefore be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass.
 
Masteron is often an ideal choice for inclusion in a steroid stack, or in some cases for use as the sole injectable for a steroid cycle.Androgens and assimilation hormonal.
 
An enanthate ester version having a half-life of probably 5 days has become available. This version of Masteron may be injected as infrequently as twice per week.
 

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Melanocyte Stimulating Hormone

Melanocyte Stimulating Hormones are a class of peptide hormones that in nature are produced by cells in the intermediate lobe of the pituitary gland.It stimulate the production and release of melanin (melanogenesis) by melanocytes in skin and hair.It is generated through the cleavage of a precursor protein called proopiomelanocortin (POMC).It is known to influence behaviour, to suppress appetite, and to increase the total amount of pigment in the skin.Melanocyte-stimulating hormone reduces UV-induced DNA damage through the induction of pigmentation.

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2
 
Basic Info.
 
Product Name: 
Melanotan 2; MT2; Melanotan-II; Melanotan2
CAS: 121062-08-6
Molecular Formula: C50H69N15O9
Molecular weight: 1024.2
Purity (by HPLC): 99.00%
Appearance: White Powder
Sequence: Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-NH2
Storage Condition: away from light, cold storage (2-8 degree)
Usage: prevention sunlight-induce skin cancer; Sexual Dysfunction & Fat Decomposition
 
What is Melanotan 2 ?
Melanotan 2  Tanning Injections (otherwise known as MT2) was first synthesized at the University of Arizona.  Researches there knew that onc of the best defenses against skin cancer was melanin activated in the skin, a tan.  They hypothesized that an effective way to reduce skin cancer rates in people would be to induce the body's natural pigmentary system to produce a protective tan prior to UV exposure.  The body's naturally occuring hormone MSH causes melanogenesis, a process by which the skin's pigment cells (melanocytes) produce the skin's pigment (melanin).  They tested to see if administering this endogenous hormone to the body directly could be an effective method to cause sunless tanning.  What they found was that while it appeared to work, natural MSH had too short a half life in the body to be practical as a therapeutic drug.  So they decided to find a more potent and stable alternative, one that would be more practical.
 
After synthesizing and screening hundreds of molecules, the researchers headed by Victor J. Hruby and Mac E. Hadley, found a peptide, [Nle4, D-Phe7] MSH, that was approimately 1,000 times more potent than the natural MSH.  They dubbed this new peptide molecule, "Melanotan" (later Melanotan-1, now know as afamelanotide).  They subsequently developed another analog, Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2), which they called "Melanotan" Tanning Injections.  The scientists hoped to use these peptides to combat melanoma by stimulating the body's natural pigmentary mechanism to create a tan without first needing exposure to harmful levels of UV radiation.  This in turn, they hypothesized, could reduce the potential for skin damage that can eventually lead to skin cancer.
 
A pilot phase I clinical trial conducted on three males by the College of Medacine, Pharmacology Department, University of Arizona in Tuscon, Arizona pulished in 1996 reported that, "Melanotan" Tanning Injections has tanning activity in humans given only 5 low doses every other day by subcutaneous injection."  The side effects reported were mild nausea and a "stretching and yawning complex" that correlated with spontaneous penile erections.
 
The Department of Pharmacology, University of Arizona College of Medacin published in 1998 that involved 10 men who suffered from psychogenic erectile dysfunction.  Their trial concluded that, "Melanotan" Tanning Injections is a potent initiator of erections in men with pyschogenic erectile dydfunction and has manageable side effects at a dose of 0.025mg/kg.
 
A clinical study published in 2000 of 20 men with psychogenic and organic erectile dysfunction conducted at the Section of Urology of The University of Arizona College of Medacin concluded, "that Melanotan II Tanning Injections is a potent initiator of penile erection in men with ecrectile dysfunction.
 
How to use Melanotan 2 Mixing the solutionv:
 
Flip off the cap from the Melanotan 2 Tanning Injection vial.
Wipe the surface of the top of the vial with the enclosed alcohol wipe and discard the wipe.
Wipe the surface of the injectable water tube (or glass water vial depending on the pack ordered) with the enclosed alcohol wipe and discard the wipe.
Remove the enclosed syringe from the packaging. Making sure the injectable water tube is upright, insert the needle of the syringe into the sidewall of the water.
Now pull back the plunger of the syringe so you withdraw 1ml of water and slowly pull the syringe out.
Insert the syringe into the Melanotan 2 Tanning Injection vial and depress the plunger so you completely empty the syringe of the water and slowly remove the syringe from the vial.  Do not shake the solution.
Place the Melanotan 2 solution in the fridge for storage until ready for use.
Make sure you put the syringe caps on and carefully dispose of it.
You have now mixed your Melanotan 2 Tanning Injection solution. Please store the solution in the fridge.
 
How to use Melanotan II for tanning?
 
Melanotan II is typically provided in vials containing 10 mg of lyophilized (freeze-dried) powder. The vials are reconstituted with a convenient amount of bacteriostatic or sterile water, added to the vial by syringe. An example convenient amount of water is 2.5 mL. When this amount of water is used, the resulting solution contains 4 mg of MT-II per mL. If for example wishing to take a dose of 1 mg, a volume of 0.25 mL, or "25 IU" as marked on an insulin syringe, would be taken by injection. Injection may be subcutaneous, intramuscular, or intravenous, according to personal preference.
 
Injection typically is only once per day, but where a person is first trying the drug and judging tolerance, injection may be divided into two smaller amounts per day.
Typical dosage range is 0.5 to 2.0 mg/day, with a preferred range of 0.5 to 1.0 mg/day. However, it's best to first assess tolerance with lower dosing of 0.25 mg at a time.
After reconstitution, a Melanotan II vial should preferably be consumed entirely within 30 days. Prior to reconstitution, MT-II should be stored in the refrigerator or freezer, but it's acceptable for it to be shipped without refrigeration.
 
Use generally should be discontinued if MT-II, in the individual case, causes problems with increased growth, number, or darkness of moles.
 
Melanotan II's effect is fairly long-lasting. It can even be the case that it takes a year or more for a cycle's effect to largely disappear. Use of maintenance cycles can maintain effect indefinitely. As a rule of thumb, maintenance typically requires about 2 to 3 times as much MT-II per year as was needed for the first cycle. This can be taken either as a total of 2 to 3 cycles per year done in the same way as the initial cycle, or any more frequent dosing pattern providing this total amount of MT-II per year.
 

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Mesterolone USP 99%

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Androviron 99% Purity Raw Steroid Powders Mesterolone For Bodybuilding Steroids 1424-00-6
 
Mesterolone Basic Info.
 
Product Name: Mesterolone
Synonyms: 17-beta-hydroxy-1-alpha-methyl-5-alpha-androstan-3-on; 1-alpha-methyl-17-beta-hydroxy-5-alpha-androstan-3-one; Androviron; Mesteranum; Mesterolon
CAS: 1424-00-6
MF: C20H32O2
MW: 304.47
Assay: 99% min.
Packing: 1kg foil bag
Characteristic: White crystalline powder.
Categories: Biochemistry; Hydroxyketosteroids; Steroids
Usage: Pharmaceutical material, Steroid hormone, Anabolin. For the treatment of male hypogonadism and reduced sperm infertility. 
 
Mesterolone Description:
 
Mesterolone is an oral anabolic steroid, a synthetic product of the male hormone testosterone. The drug has shown value in treating men with mental health issues, such as depression, anxiety and bipolar disorders. The drug also is commonly used to treat sexual dysfunction, including low sperm count. Additionally, mesterolone may enhance the effectiveness of other steroids. Interestingly, unlike other steroids, the drug shows little value for bodybuilding, but has the same health risks involved in steroid use for that purpose.
 
Mesterolone Applications:
 
Mesterolone is often used as an antiestrogenic treatment and may be used by those who have had a poor reaction to testosterone treatments. The drug has shown to be beneficial in treating sexual dysfunction, impotency and low libido. Mesterolone binds to estrogen receptors, reducing their activity, which not only reduces estrogen production, but also encourages natural testosterone production in the body.
During the late 1970s, doctors who performed studies on mesterolone concluded that the drug could be used to treat depression in some men. Patients with symptoms of anxiety and low sex drive reported improvement with low doses of the steroid. During the study, higher doses proved helpful to patients with dysthymia and bipolar depression as well. Since this time, newer studies have shown that patients taking a placebo improved at the same rate as patients taking mesterolone, leading medical professionals to believe that better drug options exit.
 

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