![structure of [3,2-c]Pyrazole-5α-androstan-17β-ol](https://molwiki.oss-cn-hongkong.aliyuncs.com/structure/No structure.png)
[3,2-c]Pyrazole-5α-androstan-17β-ol
CAS No.:
99996-65-3
M. Wt:
314.465
M. Fa:
C20H30N2O
InChI Key:
-
Names and Identifiers of [3,2-c]Pyrazole-5α-androstan-17β-ol
CAS Number |
99996-65-3 |
|---|
Physical and chemical properties of [3,2-c]Pyrazole-5α-androstan-17β-ol
Boiling Point |
491.4±45.0 °C at 760 mmHg |
|---|---|
Density |
1.2±0.1 g/cm3 |
Exact Mass |
314.235809 |
Flash Point |
251.0±28.7 °C |
Index of Refraction |
1.585 |
LogP |
4.99 |
Molecular Formula |
C20H30N2O |
Molecular Weight |
314.465 |
Vapour Pressure |
0.0±1.3 mmHg at 25°C |
Applications of [3,2-c]Pyrazole-5α-androstan-17β-ol
17alpha-Demethylated stanozolol has various applications:
- Medical Use: Initially developed for treating conditions like muscle wasting and osteoporosis.
- Athletic Performance: Widely used in sports for its performance-enhancing properties despite being banned by most sports organizations due to its potential for abuse.
- Veterinary Medicine: Utilized in veterinary practices to promote growth in livestock and enhance recovery from injury.
Interaction Studies of [3,2-c]Pyrazole-5α-androstan-17β-ol
Studies have shown that 17alpha-Demethylated stanozolol interacts with various biological systems:
Similar CompoundsSeveral compounds share structural similarities with 17alpha-Demethylated stanozolol. Here are some notable examples:
| Compound Name | Structural Features | Unique Aspects |
|---|---|---|
| Testosterone | Natural androgen; not alkylated | Strong androgenic effects; aromatizes to estrogen |
| Nandrolone | 19-nor derivative of testosterone | Lower androgenic activity; commonly used in therapy |
| Methandienone | 17α-alkylated; similar anabolic properties | Known for rapid muscle gain but higher side effects |
| Oxandrolone | Mild anabolic steroid; less potent | Often used for cutting cycles due to lower weight gain |
| Mesterolone | Dihydrotestosterone derivative; less anabolic | Primarily used for male hormone replacement therapy |
Biological Activity of [3,2-c]Pyrazole-5α-androstan-17β-ol
17alpha-Demethylated stanozolol exhibits notable biological activities, including:
- Anabolic Effects: It promotes muscle growth and strength gains by enhancing protein synthesis and nitrogen retention.
- Androgenic Effects: While it has some androgenic activity, its effects are significantly milder than those of testosterone, minimizing side effects such as hair loss and acne.
- Diuretic Properties: The compound has been noted for its diuretic effects, which can lead to temporary weight loss through fluid reduction.
- Non-aromatization: Unlike many anabolic steroids, 17alpha-Demethylated stanozolol does not convert to estrogen, reducing the risk of estrogenic side effects such as gynecomastia.