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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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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9

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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene
 
Clomid Basic Info.:
 
Product Name: Clomid (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
 
Clomid Description:
 
Clomid is a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, puts it in 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. Without the binding of the cofactor, the estrogen receptor is inactive. Different tissues use different cofactors. Some of these cofactors are able to bind to the estrogen receptor/Clomid complex, but others are blocked due to the change in shape. The result is that in some tissues Clomid acts as an antagonist - the cofactor used in that tissue cannot bind and so the receptor remains inactive - and in others Clomid acts as an agonist (activator), because the cofactors used in that tissue are able to bind. 
 
Clomid Applications:
 
Steroids Hormone Clomiphene Citrate/Clomid powders/CAS No: 50-41-9
Clomid is the anti-estrogen of choice for improving recovery of natural testosterone production after a cycle, improving testosterone production of endurance athletes, and is also effective in reducing risk of gynecomastia during a cycle employing aromatizable steroids. 
 

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GMP Standard Active Pharmaceutical Ingredient Bupivacaine HCl /Bupivacaine Hydrochloride 14252-80-3

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GMP Standard Active Pharmaceutical Ingredient Bupivacaine HCl /Bupivacaine Hydrochloride 14252-80-3
 
Bupivacaine HCL Basic Info.
 
Product Name: Bupivacaine Hydrochloride
Synonyms: Bupivacaine hydrochloride; Bupivocoine HCl; Sensorcaine;
CAS No.: 14252-80-3
EINECS No.: Bupivacaine Hydrochloride 
Molecular formula: C18H28N2O.ClH
Hydrochloride Molecular weight: 324.89
Hydrochloride Appearance: White crystalline powder
Hydrochloride Content: 99%Bupivacaine Hydrochloride Packing: 1KGS/Bag; 25KGS/DrumBupivacaine Hydrochloride Grade: Pharmaceutical gradeBupivacaine Hydrochloride Category: Pharmaceutical raw material
 
Bupivacaine HCL Description:
 
Anesthesia, local- Proparacaine and tetracaine are indicated to produce local anesthesia of short duration for ophthalmic procedures including measurement of intraocular pressure, removal of foreign bodies and sutures, and conjunctival and corneal scraping in diagnosis and gonioscopy.
 
Bupivacaine HCL Applications:
 
Proparacaine hydrochloride and tetracaine are also indicated to produce local anesthesia prior to surgical procedures such as cataract extraction and pterygium excision, usually as an adjunct to locally injected anesthetics.
Ophthalmic solutions used for intraocular procedures should be preservative-free. Preservatives may cause damage to the corneal epithelium if a significant quantity of solutionenters the eye through the incision.
 

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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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Treatment Receptor Metastatic Drug Fulvestrant / Faslodex 129453-61-8 Anti Cancer Steroids Raw Powder

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Treatment Receptor Metastatic Drug Fulvestrant / Faslodex 129453-61-8 Anti Cancer Steroids Raw Powder
 
Fulvestrant Basic Info.:
 
Product Name: Fulvestrant
Synonyms: Faslodex
Chemical Name: (7a,17b)-7-[9-[(4,4,5,5,5-Pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17-diol
CAS: 129453-61-8
Molecular Fomular: C32H47F5O3S
Molecular Weight: 606.77
Purity: 99%
Appearance: White powder
Density: 1.201 g/cm3
Melting Point: 104-106°C
Boiling Point: 674.8 °C at 760 mmHg
Package: 10g/foil bag
Usage: To treat estrogen receptor positive metastatic breast cancer in postmenopausal women, with disease progression following antiestrogen therapy.
 
Fulvestrant Description:
 
Fulvestrant also called Faslodex or AstraZeneca,is is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It works by blocking the actions of estrogen in the body. Fulvestrant is a complete estrogen receptor antagonist with no agonist effects, which in addition, accelerates the proteasomal degradation of the estrogen receptor. The drug has poor oral bioavailability, and is administered monthly via intramuscular injection.Certain types of breast cancer use estrogen to grow and multiply in the body.do not use fulvestrant if you are allergic to any ingredient in fulvestrant ,and Contact your doctor or health care provider right away if any of these apply to you.
 
Fulvestrant Applications:
 
Many breast cancers are stimulated to grow by the female sex hormones oestrogen and progesterone. These breast cancers are called hormone sensitive or hormone receptor positive. Drugs that block the effects of these hormones can slow or stop the growth of the breast cancer cells. Fulvestrant stops oestrogen getting to the cancer cells by blocking oestrogen receptors and reducing the number of receptors the cancer cell has.
 
Fulvestrant Acetate (Faslodex, AstraZeneca) is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It is an estrogen receptor antagonist with no agonist effects, which works by down-regulating the estrogen receptor.
 
Fulvestrant Acetate is a selective estrogen receptor down-regulator (SERD). Fulvestrant is indicated for the treatment of hormone receptor positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. The dosing schedule for fulvestrant remains under investigation in an attempt to optimize its effectiveness.
 

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