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anabolic steroid hormones
Cabergoline Dostinex Caber Anti Estrogen Supplements Muscle Building Steroids 81409-90-7
Cabergoline is used to treat different types of medical problems that occur when too much of the
Hormone prolactin is produced. It can be used to treat certain menstrual problems, fertility problems
In men and women, and pituitary prolactinomas (tumors of the pituitary gland). It works by stopping
The brain from making and releasing the prolactin hormone from the pituitary
Cabergoline use is usually stopped when prolactin levels are normal for 6 months. It may be given
Again if symptoms of too much prolactin occur again.
Originally introduced by the anti-aging community to the bodybuilding world, this dopamine receptor agonist has the chemical name of 1-[(6-allylergolin-8? -yl)-carbonyl]-1-[3-(dimethylamino) propyl]-3-ethylurea and tablets of this drug include 0.5 mg of cabergoline and the list of inactive ingredients includes leucine, USP, lactose, and NF.
Dostinex-Cabergoline has a chemical name of 1-[(6-allylergolin-8? -yl)-carbonyl]-1-[3-(dimethylamino) propyl]-3-ethylurea. The empirical formula for this drug is C26H37N5O2 and its molecular weight is 451.62.
Dostinex, also called cabergoline (or just caber), is a dopamine agonist drug used in medicine, which is also popular in the bodybuilding world, where it is used to keep prolactin low during steroid cycles. Medically, it is used in males with hyperprolactinemia, reduced sperm production, impotency, and low sex drive.
Cabergoline is a dopamine agonist designed to reduce prolactin. In medical circles it is commonly used to combat prolactinomas, a benign tumor of the pituitary gland that may cause an excess production of prolactin. It is also used by athletes who supplement with anabolic steroids that may increase prolactin levels such as Nandrolone and Trenbolone.
Cabergoline, most commonly sold under the brand name Dostinex, is not a new drug as it was first developed in 1981 by the Italian drug manufacture Farmitalia-Carlo Erba Spa. The drug was later acquired by Pharmacia and then found its resting place with Pfizer in 2002.
Dexamethaslo Application :
Cabergoline is used to treat high levels of prolactin hormone in your body. High levels of prolactin in women can cause symptoms such as unwanted breast milk and missed periods and can cause difficulty becoming pregnant. High levels of prolactin in men can cause symptoms such as enlarged breasts and decreased sexual ability/desire. Cabergoline is an ergot medication and works by blocking the release of prolactin from the pituitary gland.
Cabergoline will help you reduce the chance of any of these prolactin related side-effects. It has actually been shown in numerous studies to have a very high success rate in lowering prolactin and prolactin related conditions and side-effects. In fact, for management of hyperprolactinemia and it's symptoms.
As a dopamine agonist, Cabergoline directly correlates with the long acting D2 receptor thereby inhibiting the secretion of prolactin in the body and in turn lowering serum prolactin levels. As a dopamine agnonist, Cabergoline is used to treat Parkinson’s disease, hyperprolactinaemia (abnormally high levels of prolactin in the blood), Cushing’s disease and as mentioned prolactinomas.
Cabergoline’s direct function (specifics) is in that it inhibits prolactin secretion in the pituitary’s lactotroph cells. It really is a very simple drug and what’s simpler or perhaps interesting is that the simple medication was discovered almost accidently during experiments with ergot alkaloids
|Description||White or almost white crystarlline powder||Conforn|
|Identify||1. IR complies
2. X-Ray complies
3. HPLC complies
|Water||No more than 0.5%||0.2%|
|Reiated substances||1. Allylamide (USP, rel, D) no more than 0.10%
2. Allyl DHLA(USP, rel, D) no more than 0.15%;
3. Cabergoline oxide no more than 0.10%;
4. Other impurities individually no more than 0.10%;
5. Total no more than 0.50%;
Less than 0.02%
Less than 0.02%
Less than 0.02%
|Opdical rotation||-83.0-- -77.0||-78|
|Residual Solvents||1. Dichloromethane no more than 100ppm;
2. Acetone no more than200ppm;
3. Tert-butylmethylether no more than 200ppm;
4. Xylene no more than 1500ppm;
5. HEptane no more than 1000ppm;
|Residue on ignition||NO more than0.10 %||0.02%|
|Heavy metals||NO more than 20ppm||2ppm|
|Partcle size||90%af particles no mone than 80μm||Conform|
|Conclusion||Conforn with EP6.0/ USP38|
|SARM (Raw Powder)|
|GHRP-6||IGF-1 LR3||Anastrozole (Arimidex)|
|CJC-1295 with DAC||IGF-1 DES||Boldenone|
|CJC-1295 NO DAC||Follistatin||Boldenone undecylenate (EQ)|
|Thymosin β4 (TB500)||EPO||Nolvadex|
|Melanotan-II (MT-II)||Tadalafil (Cialis)|
|Melanotan-I (MT-I)||SARM||Letrozole (Femara)|
|Triptorelin||LGD-4033 (Ligandrol)||Methenolone Acetate|
|GHRH||YK-11||Stanozolol Coarse (Winstrol)|
|Tesamorelin||Aicar||Stanozolol Micronized (Winstrol)|
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