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Boldenone was synthesized in an attempt to create a long-acting injectable methandrostenolone (Dianabol), but in reality boldenone acts nothing like methandrostenolone. It has a very long half-life, and can show up on a steroid test for up to 1.5 years, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use. Although commonly compared to nandrolone, boldenone lacks progesterone receptor interaction and all the associated progestogenic side effects. Tel:00862781331422 Fax:00862781331422 Cel:+8615337164625 Skyepe:leslie(at)carphetin(dot)com Email:leslie(at)carphetin(dot)com
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Product Name: Stanozolol/Winstrol
Chemical name:17-alpha-methyl-5-alpha-androstano(3,2-c)pyrazol-17-beta-ol
CAS No.: 10418-03-8
MF: C21H32N2O
MW: 328.49
EINECS: 233-894-8
Appearance: White crystalline powder
USP31/BP2007
Assay: 98% min
Storage: Ventilation low temperature drying Delivery: priority to the use of DHL, TNT, FedEx, HKEMS, UPS,TOll etc.
Arimidex (generic name is anastrozole) is a newer drug developed for the treatment of advanced breast cancer in women. It is manufactured by Zenica Pharmaceuticals and was approved for use in the United States at the end of December 1995. Specifically, Arimidex is the first in a new class of third-generation selective oral aromatase inhibitors. It acts by blocking the enzyme aromatase, subsequently blocking the production of estrogen. Since many forms of breast cancer cells are stimulated by estrogen, it is hoped that by reducing amounts of estrogen in the body the progression of such a disease can be halted. This is the basic premise behind Nolvadex, except this drug blocks the action and not production of estrogen. The effects of Arimidex can be quite dramatic to say the least. A daily dose of one tablet (1 mg) can produce estrogen suppression greater than 80 % in treated patients. With the powerful effect this drug has on hormone levels, it is only to be used (clinically) by post-menopausal women whose disease has progressed following treatment with Nolvadex (tamoxifen citrate). Side effects like hot flushes and hair thinning can be present, and would no doubt be much more severe in pre-menopausal patients. There are some concerns with using an aromatase inhibitor such as this during prolonged steroid treatment however. While it will effectively reduce estrogenic side effects, it will also block the beneficial properties of estrogen from becoming apparent (namely its effect on cholesterol values). Studies have clearly shown that when an aromatase inhibitor is used in conjunction with a steroid such as testosterone, suppression of HDL (good) cholesterol becomes much more pronounced. Apparently estrogen plays a role in minimizing the negative impact of steroid use. Since the estrogen receptor antagonist Nolvadex is shown not to display an anti-estrogenic effect on cholesterol values, it is certainly the preferred from of estrogen maintenance for those concerned with cardiovascular health. Tel:00862781331422 Fax:00862781331422 Cel:+8615337164625 Skyepe:leslie(at)carphetin(dot)com Email:leslie(at)carphetin(dot)com
Norgestimate is a molecule used in hormonal contraceptives. It is a form of progesterone, which is a female hormone important for the regulation of ovulation and menstruation. It is used with estradiol, to treat the symptoms of menopause.
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Trimegestone is a steroidal progestin of the 19-norprogesterone group related to promegestone. Trimegestone has very high affinity for the progesterone receptor, only weak affinity for the mineralocorticoid receptor, and little or no affinity for other steroid hormone receptors. It is used as a hormonal contraceptive and in hormonal replacement therapy for postmenopausal symptoms.
Levothyroxine is a synthetically prepared levo isomer of thyroxine, the major hormone secreted from the thyroid gland. It is used as a hormone replacement for patients with thyroid problems. It is used to treat hypothyroidism, goiter, chronic lymphocytic thyroiditis, myxedema coma, and stupor.
Norethindrone is a synthetic progestational hormone with actions similar to those of progesterone but functioning as a more potent inhibitor of ovulation. It has weak estrogenic and androgenic properties.It is a molecule used in some combined oral contraceptive pills, progestogen only pills and is also available as a stand-alone drug. It is a progestogen and can be used to treat premenstrual syndrome, painful periods, abnormal heavy bleeding, irregular periods, menopausal syndrome (in combination with oestrogen), or to postpone a period. It is also commonly used to help prevent uterine hemorrhage in complicated non-surgical or pre-surgical gynecologic cases. Norethindrone was the first orally highly active progestin to be synthesized.
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