ent-17-Hydroxykaur-15-en-19-oic acid
ent-17-Hydroxykaur-15-en-19-oic acid Basic information
- Product Name:
- ent-17-Hydroxykaur-15-en-19-oic acid
- Synonyms:
-
- ent-17-Hydroxykaur-15-en-19-oic acid
- 17-Hydroxy-ent-kaur-15-en-19-oic acid
- Kaur-15-en-18-oic acid, 17-hydroxy-, (4α)-
- CAS:
- 35030-38-7
- MF:
- C20H30O3
- MW:
- 318.46
- Mol File:
- 35030-38-7.mol
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ent-17-Hydroxykaur-15-en-19-oic acid Chemical Properties
- Melting point:
- 187-188 °C
- Boiling point:
- 477.9±38.0 °C(Predicted)
- Density
- 1.17±0.1 g/cm3(Predicted)
- pka
- 4.68±0.60(Predicted)
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ent-17-Hydroxykaur-15-en-19-oic acid Usage And Synthesis
Uses
ent-17-Hydroxykaur-15-en-19-oic acid is a ent-kaurene diterpene that can be isolated from the leaves of Laetia thamnia L.. ent-17-Hydroxykaur-15-en-19-oic acid was cytotoxic to human prostate LNCaP2 cells with IC50 17.63 mg/mL[1].
References
[1] Pugazhendhi, D et al. “Effect of sulphation on the oestrogen agonist activity of the phytoestrogens genistein and daidzein in MCF-7 human breast cancer cells.” The Journal of endocrinology vol. 197,3 (2008): 503-15. doi:10.1677/JOE-07-0384 DOI:10.1677/JOE-07-0384
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