Hormone drugs used in treating deficient hormone levels in body, thyroid problems, ovulation

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8 
 
Raloxifene HCL Basic Info.:
 
Product Name: Raloxifene Hydrochloride
Synonyms: Raloxifene HCL;Raloxifene Hydrochloride;Ly156758;Piperidin;Keoxifene;Keoxifene Hydrochloride;Ly 139481;AKOS 92138
CAS: 82640-04-8
MF: C28H28ClNO4S
MW: 510.04
Melting Point: 250-253°C
Storage Temp.: -20°C Freezer
Solubility DMSO: 28 mg/mL, soluble
Chemical Properties: Light-Yellow Solid
Assay: 99%
Grade: Pharmaceutical Grade
Product Categories: Active Pharmaceutical Ingredients;Raloxifene;Intracellular receptor;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Pharmaceutical intermediate;API;Inhibitors;antifungal
Usage: amino acid, nutrient, Labeled Raloxifene, intended for use as an internal standard for the quantification of Raloxifene by GC- or LC-mass spectrometry.A nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic.
 
Product Description:
 
Raloxifene HCL(marketed as Evista) is an oral selective estrogen receptor modulator (SERM) that has estrogenic actions on bone and anti-estrogenic actions on the uterus and breast. It is used in the prevention of osteoporosis in postmenopausal women and to reduce the risk of invasive breast cancer in postmenopausal women with osteoporosis and in postmenopausal women at high risk for invasive breast cancer.
 
This drug is different from hormones (including estrogens and progestins). It works by acting like estrogen (as a selective estrogen receptor modulator or SERM) in some parts of the body. Raloxifene HCL helps to preserve bone mass, but it does not affect the breast and uterus like estrogen or relieve symptoms of menopause such as hot flashes.
 
Raloxifene HCL is indicated for the treatment and prevention of osteoporosis in postmenopausal women. It is also used for reduction of risk and treatment of invasive breast cancer, and it also reduces breast density.For either osteoporosis treatment or prevention, supplemental calcium and/or vitamin D should be added to the diet if daily intake is inadequate.
 
Raloxifene HCL is used to prevent and treat bone loss (osteoporosis) in women after menopause. Maintaining strong bones by slowing bone loss helps to reduce the risk of fractures.
 
Raloxifene HCL may also lower the chance of getting a certain type of breast cancer (invasive) in women after menopause.
 

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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0

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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0
 
Estradiol Enanthate Basic Info.
 
Product Name: Estradiol Enanthate
CAS Number: 4956-37-0
Purity: 99%
Molecular Weight: 384.556
Molecular Formula: C25H36O3
Appearance: Crystalline powder
Physical State: Solid
Solubility: Soluble in water (slightly).
Storage: Store at room temperature
Melting Point: 94-96 ° C
Boiling Point: ~509.5 ° C at 760 mmHg (Predicted)
Density: ~1.1 g/cm3 (Predicted)
 
Estradiol Enanthate Description:
 
Estradiol enanthate (INN, USAN), or estradiol enantate, is a synthetic ester, specifically the 17-heptanoyl ester, of the natural estrogen, estradiol. It is marketed under the brand names Anafertin, Deladroxate, Perlutan, and Topasel, which are combination formulations of estradiol enanthate and dihydroxyprogesterone acetophenide, as a once-monthly injectable hormonal contraceptive in Spain and Latin America, and has been used as such since at least the mid-1960s.
 
Estradiol, or more precisely, 17β-estradiol, is a human sex hormone and steroid, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species.
 
Estradiol or oestradiol (American or British English usages), derives from estra-, Gk. οστρο? (oistros, literally meaning "verve or inspiration") and -diol, a chemical name and suffix indicating that this form of steroid and sex hormone is a type of alcohol bearing two hydroxyl groups.
 
Estradiol is produced especially within the follicles of female ovaries, but also in other endocrine (i.e., hormone-producing) and non-endocrine tissues (e.g., including fat, liver, adrenal, breast, and neural tissues). Estradiol is biosynthesized from progesterone (arrived at in two steps from cholesterol, via intermediate pregnenolone). One principle pathway then converts progesterone to its 17-hydroxy-derivative, and then to androstenedione via sequential cytochrome P450-catalyzed oxidations.Action of aromatase on this dione generates estrone, and action of a dehydrogenase on this gives the title compound, 17β-estradiol.
 
Estradiol Enanthate Function:
 
Hormones and Regulation of Endocrine Function of Drug, Nutritional Therapeutics, Antibiotic and Antimicrobial Agents, Antiparasitic, Original Drug Resistant Microbes, Immune System Drugs, Specialist Drugs, Drug Detoxification, Diagnostic Agents, Blood System Agents, Visceral System Medication, Central Nervous System Agents, Cardiovascular Agents, Urinary System Agents, Respiratory System Agents.
 
A chemical derivative of estradiol, ethinyl estradiol with maximum dosage 200 µg, is a major component of hormonal contraceptive devices. Combined forms of hormonal contraception contain ethinyl estradiol and a progestin, which both contribute to the inhibition of GnRH, LH, and FSH, which accounts for the ability of these birth control methods to prevent ovulation and thus prevent pregnancy. Other types of hormonal birth control contain only progestins and no ethinyl estradiol.
 

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High Quality Legal Anabolic Steroids Trestolone For Muscle Growth 3764-87-2

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High Quality Legal Anabolic Steroids Trestolone For Muscle Growth 3764-87-2
 
Trestolone Basic Info.
 
Product Name: Trestolone
Synonyms: 19-Nor-7A-Methyltestosterone;7-Alpha-Methyl-19-Nortestosterone;
CAS: 3764-87-2
Molecular formula: C19H28O2
Molecular weight: 288.42
Appearance: white crystalline powder
Product Categories: Steroid and Hormone.
Usage: Trestolone is a synthetic androgen used as a potential hormonal male contraceptive method that induces a state of termporary infertility.
 
Trestolone Description:
 
Trestolone is a synthetic androgen taken to build muscle rapidly, and is a theoretical candidate drug for use in hormonal male contraceptive methods. In males, regular administration of sufficient quantities of trestolone induces a state of temporary infertility
 
Trestolone is an experimental contraceptive treatment and is not yet available commercially. It is currently being evaluated for safety and effectiveness in scientific studies, supported by the Population Council.
 
As a derivative of the anabolic steroid hormone nandrolone, trestolone's viability as a male contraceptive is twofold.
 
Trestolone Usage:
 
Trestolone is a synthetic androgen used as a potential hormonal male contraceptive method that induces a state of termporary infertility.
 

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High Quality Local Anesthetic Prilocaine Hydrochloride Prilocaine HCl 1786-81-8

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High Quality Local Anesthetic Prilocaine Hydrochloride Prilocaine HCl 1786-81-8
 
Prilocaine HCL Basic Info.:
 
Product Name: Prilocaine HCL
CAS: 1786-81-8
English name: Propitocaine hydrochloride
Other name: Prilocaine hydrochloride; 2 - propylamine base - o C amide toluene hydrochloride; Prilocaine hydrochloride; Prilocaine hydrochloride
Molecular formula: C13H21ClN2O
EINECS: 217-244-0
Molecular Weight: 256.7716
 
Prilocaine HCL Description:
 
Propitocaine hydrochloride is a local anesthetic of the amino amide type first prepared by Claes Tegner and Nils Lö Fgren. In its injectable form, it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used forintravenous regional anaesthesia.
 
In some patients, a metabolite of prilocaine may cause the unusual side effect of methemoglobinemia, which may be treated with methylene blue.
 
Local anesthetic is a substance that causes loss of sensation only to the area to which it is applied without affecting consciousness. Most local anesthetics structures have amino-ester or an amino-amide group which are linked to hydrophilic (secondary or tertiary amine) and to hydrophobic group (aromatics) on the other side.
 
Local anesthetics, long duration, lower toxicity, chemicals that are also small Suitable for epidural anesthesia, block anesthesia and infiltration anesthesia, etc.
 

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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 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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