11a-Hydroxy-16,17a-epoxyprogesterone
97%
- Product Code: 96608
CAS:
19427-36-2
| Molecular Weight: | 344.44 g./mol | Molecular Formula: | C₂₁H₂₈O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 508.7±50.0℃(Predicted) | |
| Density: | 1.25±0.1g/ml(Predicted) | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
11a-Hydroxy-16,17a-epoxyprogesterone is primarily utilized in the field of pharmaceutical research and development, particularly in the study of steroid hormones and their derivatives. Its unique structure makes it a valuable intermediate in the synthesis of more complex steroid compounds, which are often explored for their potential therapeutic effects. Researchers investigate its role in modulating hormonal pathways, which can lead to the development of drugs targeting conditions such as hormonal imbalances, reproductive disorders, and certain types of cancers. Additionally, its epoxy and hydroxyl groups provide reactive sites for further chemical modifications, enabling the creation of novel analogs with enhanced biological activity or specificity. This compound is also of interest in understanding the biochemical mechanisms of steroid metabolism and receptor interactions, contributing to advancements in endocrinology and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | Ft38,592.85 |
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| 0.050 | 10-20 days | Ft115,390.70 |
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| 0.250 | 10-20 days | Ft349,081.10 |
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11a-Hydroxy-16,17a-epoxyprogesterone
11a-Hydroxy-16,17a-epoxyprogesterone is primarily utilized in the field of pharmaceutical research and development, particularly in the study of steroid hormones and their derivatives. Its unique structure makes it a valuable intermediate in the synthesis of more complex steroid compounds, which are often explored for their potential therapeutic effects. Researchers investigate its role in modulating hormonal pathways, which can lead to the development of drugs targeting conditions such as hormonal imbalances, reproductive disorders, and certain types of cancers. Additionally, its epoxy and hydroxyl groups provide reactive sites for further chemical modifications, enabling the creation of novel analogs with enhanced biological activity or specificity. This compound is also of interest in understanding the biochemical mechanisms of steroid metabolism and receptor interactions, contributing to advancements in endocrinology and drug discovery.
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