Molecular structure of Androst-16-en-3-ol, CAS Number: 7148-51-8
Androst-16-en-3-ol (CAS 7148-51-8)
Alternate Names:
3β-Androstenol
Application:
Androst-16-en-3-ol is A metabolite of 16-Androstene
CAS Number:
7148-51-8
Purity:
≥98%
Molecular Weight:
274.44
Molecular Formula:
C19H30O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Androst-16-en-3-ol is an organic compound that falls under the category of steroidal pheromones. Its structure is closely related to that of other androstane steroids, and it has been extensively studied for its role in olfactory communication among mammals. Researchers have concentrated on Androst-16-en-3-ol for its potential applications in understanding animal behavior, particularly in relation to reproductive signaling and territorial marking. In the agricultural sector, studies have been conducted to explore its influence on livestock and its potential to modify or influence animal husbandry practices. Additionally, Androst-16-en-3-ol has been a point of interest in the field of chemical ecology as a means to understand the evolutionary aspects of pheromonal communication.
Androst-16-en-3-ol (CAS 7148-51-8) References
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- The pheromone androstenol (5 alpha-androst-16-en-3 alpha-ol) is a neurosteroid positive modulator of GABAA receptors. | Kaminski, RM., et al. 2006. J Pharmacol Exp Ther. 317: 694-703. PMID: 16415088
- Relationship between the expression of hepatic but not testicular 3beta-hydroxysteroid dehydrogenase with androstenone deposition in pig adipose tissue. | Nicolau-Solano, SI., et al. 2006. J Anim Sci. 84: 2809-17. PMID: 16971583
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- Development of a candidate reference method for the simultaneous quantitation of the boar taint compounds androstenone, 3α-androstenol, 3β-androstenol, skatole, and indole in pig fat by means of stable isotope dilution analysis-headspace solid-phase microextraction-gas chromatography/mass spectrometry. | Fischer, J., et al. 2011. Anal Chem. 83: 6785-91. PMID: 21800819
- Expression of hepatic 3β-hydroxysteroid dehydrogenase and sulfotransferase 2A1 in entire and castrated male pigs. | Rasmussen, MK., et al. 2012. Mol Biol Rep. 39: 7927-32. PMID: 22544608
- Quantitative determination of the boar taint compounds androstenone, skatole, indole, 3α-androstenol and 3β-androstenol in wild boars (Sus scrofa) reveals extremely low levels of the tryptophan-related degradation products. | Fischer, J. and Wüst, M. 2012. Food Chem. 135: 2128-32. PMID: 22980780
- Regulation of 3β-hydroxysteroid dehydrogenase and sulphotransferase 2A1 gene expression in primary porcine hepatocytes by selected sex-steroids and plant secondary metabolites from chicory (Cichorium intybus L.) and wormwood (Artemisia sp.). | Rasmussen, MK. and Ekstrand, B. 2014. Gene. 536: 53-8. PMID: 24333270
- Metabolism of androstenone, 17β-estradiol and dihydrotestosterone in primary cultured pig hepatocytes and the role of 3β-hydroxysteroid dehydrogenase in this process. | Chen, G., et al. 2015. PLoS One. 10: e113194. PMID: 25590624
- The sulfoconjugation of androstenone and dehydroepiandrosterone by human and porcine sulfotransferase enzymes. | Laderoute, H., et al. 2018. Steroids. 136: 8-16. PMID: 29792900
- The synthesis of 16-androstene sulfoconjugates from primary porcine Leydig cell culture. | Laderoute, H., et al. 2019. Steroids. 146: 14-20. PMID: 30904503
- Nuclear Receptor Pathways Mediating the Development of Boar Taint. | Bone, C. and Squires, EJ. 2022. Metabolites. 12: PMID: 36144190
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Androst-16-en-3-ol, 1 mg | sc-210815 | 1 mg | $232.00 |