5α-Androstane-3α,17β-diol
98%,100UG/MLINMETHANOL｜1ML
- Product Code: 92885
CAS:
1852-53-5
| Molecular Weight: | 292.46 g./mol | Molecular Formula: | C₁₉H₃₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00003676 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the field of endocrinology and hormone research. It serves as a key intermediate in the study of steroid metabolism, particularly in understanding the pathways and mechanisms of androgen biosynthesis and degradation. Researchers utilize it to investigate the role of androgens in various physiological processes, including male sexual development, muscle growth, and the regulation of secondary sexual characteristics. Additionally, it is employed in the development of diagnostic assays and therapeutic agents targeting androgen-related disorders, such as hypogonadism, prostate cancer, and androgen insensitivity syndrome. Its role in modulating hormone receptors also makes it valuable in studying receptor-ligand interactions and designing hormone-based treatments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $925.66 |
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5α-Androstane-3α,17β-diol
This chemical is primarily used in the field of endocrinology and hormone research. It serves as a key intermediate in the study of steroid metabolism, particularly in understanding the pathways and mechanisms of androgen biosynthesis and degradation. Researchers utilize it to investigate the role of androgens in various physiological processes, including male sexual development, muscle growth, and the regulation of secondary sexual characteristics. Additionally, it is employed in the development of diagnostic assays and therapeutic agents targeting androgen-related disorders, such as hypogonadism, prostate cancer, and androgen insensitivity syndrome. Its role in modulating hormone receptors also makes it valuable in studying receptor-ligand interactions and designing hormone-based treatments.
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