CAS 1424-00-6
:mesterolone
Description:
Mesterolone, with the CAS number 1424-00-6, is an anabolic androgenic steroid that is derived from dihydrotestosterone (DHT). It is characterized by its chemical structure, which includes a 17α-methyl group that enhances its oral bioavailability. Mesterolone is known for its relatively mild anabolic properties compared to other steroids, making it less effective for muscle mass gain but useful for enhancing strength and physical performance. It is often utilized in the treatment of male hypogonadism and certain types of infertility, as it can improve sperm production. Additionally, mesterolone has anti-estrogenic properties, which can help mitigate estrogen-related side effects in users. The substance is typically administered orally and is not commonly associated with significant water retention or aromatization to estrogen. However, like other anabolic steroids, it can have side effects, including potential impacts on liver function and hormonal balance. Its use is regulated in many countries, and it is classified as a controlled substance in various jurisdictions.
Formula:C20H32O2
InChI:InChI=1S/C20H32O2/c1-12-10-14(21)11-13-4-5-15-16-6-7-18(22)19(16,2)9-8-17(15)20(12,13)3/h12-13,15-18,22H,4-11H2,1-3H3/t12-,13-,15-,16-,17-,18-,19-,20-/m0/s1
InChI key:InChIKey=UXYRZJKIQKRJCF-TZPFWLJSSA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3)[C@@H](O)CC4)[H])(CC[C@]1(CC(=O)C[C@@H]2C)[H])[H])[H]
Synonyms:- (1Alpha,5Alpha,17Beta)-17-Hydroxy-1-Methylandrostan-3-One
- (1α,5α,17β)-17-Hydroxy-1-methylandrostan-3-one
- 17-Beta-Hydroxy-1-Alpha-Methyl-5-Alpha-Androstan-3-One
- 17β-Hydroxy-1α-methyl-5α-androstan-3-one
- 1α-Methyl-17β-hydroxy-5α-androstan-3-one
- 1α-Methyl-5α-androstan-17β-ol-3-one
- 1α-Methyl-5α-dihydrotestosterone
- 5α-Androstan-3-one, 17β-hydroxy-1α-methyl-
- Androstan-3-one, 17-hydroxy-1-methyl-, (1α,5α,17β)-
- Androviron
- Mesteranum
- Mesteronlone
- Mestoranum
- NSC 75054
- Proviron
- Provirone 25
- Sh 723
- See more synonyms
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Found 10 products.
MESTEROLONE CRS
CAS:<p>MESTEROLONE CRS</p>Formula:C20H32O2Color and Shape:Crystalline Powder. White. Light Yellow. Powder.Molecular weight:304.46691α-Methylandrostan-17β-ol-3-one
CAS:Formula:C20H32O2Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:304.47Mesterolone
CAS:Controlled Product<p>Applications Mesterolone is a synthetic androgen and a dihydrotestosterone derivative. Mesterolone is rarely used for replacement therapies due to its weak androgenic activity.<br>References Sisci, D. et al.: Adv. Contracep. Deliv. Sys., 9, 239 (1993); Petry, R. et al.: Acta Endocrinol., 59, 497 (1968); Stroemme, S.B. et al.: Med. Sci. Sports, 6, 203 (1974);<br></p>Formula:C20H32O2Color and Shape:White To Off-WhiteMolecular weight:304.47Mesterolone (1.0mg/ml in Acetonitrile)
CAS:Controlled ProductFormula:C20H32O2Color and Shape:ColourlessMolecular weight:304.4711α-Methylandrostan-17β-ol-3-one
CAS:Controlled Product<p>11alpha-Methylandrostan-17beta-ol-3-one is a pharmacological agent that belongs to the group of androgens. It is an oral preparation and has been used in the treatment of infectious diseases, autoimmune diseases, and metabolic disorders. It has also been used as a matrix effect control in biological samples. The biological effects of 11alpha-Methylandrostan-17beta-ol-3-one are mediated by its direct action on cells or through conversion to testosterone or dihydrotestosterone (DHT). These effects include increasing protein synthesis, promoting bone formation, lowering cholesterol levels, stimulating the production of red blood cells, and decreasing fat deposition. The main side effects are acne vulgaris, male pattern baldness, prostate enlargement, increased risk for prostate cancer, and increased risk for developing breast cancer.</p>Formula:C20H32O2Purity:Min. 95%Color and Shape:PowderMolecular weight:304.47 g/mol
