Open Access
Subscription Access
5α/5β Stereochemistry of Spirostanol and Furostanol Saponins
Steroidal saponins constitute an important class of plant secondary metabolites and are mostly found in monocotyledonous angiosperms. These compounds are known to possess a vast array of bioactivities, including anticancer, adjuvant, immunostimulant, anti-inflammatory, antimicrobial, hypocholesterolaemic, antimicrobial and antioxidant1,2. Structurally, steroidal saponins are classified as spirostanol and furostanol glycosides3. A third and relatively less common class of steroidal saponins is furospirostanols. The saponins of this class generally have a polyoxygenated A-ring and/or one or more double bonds present in the rings A and B4.
User
Font Size
Information
- Sparg, S. G., Light, M. E. and van Staden, J., J. Ethnopharmacol., 2004, 94, 219–243.
- Rao, A. V. and Gurfinkel, D. M., Drug Metab. Drug Interact., 2000, 17(1–4), 211–235.
- Munafo Jr, J. P. and Gianfagna, T. J., Nat. Prod. Rep., 2015, 32, 454–477.
- Xu, T. H. et al., J. Asian Nat. Prod. Res., 2008, 10(5), 415–418.
- Agrawal, P. K., Jain, D. C. and Pathak, A. K., Magn. Reson. Chem., 1995, 33(12), 923–953.
- Agrawal, P. K., Bunsawansong, P. and Morris, G. A., Phytochemistry, 1998, 47(2), 255–257.
- Agrawal, P. K., Steroids, 2005, 70(10), 715–724.
- Agrawal, P. K., Magn. Reson. Chem., 2003, 41(11), 965–968.
- Agrawal, P. K., Magn. Reson. Chem., 2004, 42(11), 990–993.
- Chen, P. Y., Chen, C. H., Kuo, C. C., Lee, T. H., Kuo, Y. H. and Lee, C. K., Planta Med., 2011, 77(9), 929–933.
- Yu, H. S. et al., Helv. Chim. Acta, 2011, 94(7), 1351–1358.
- Eskander, J., Lavaud, C. and Harakat, D., Fitoterapia, 2010, 81(5), 371–372.
- Zhang, C. L., Gao, J. M. and Zhu, W., Phytochem. Lett., 2012, 5(1), 49–52.
- Naveed, M. A., Riaz, N., Saleem, M., Jabeen, B., Ashraf, M., Ismail, T. and Jabbar, A., Steroids, 2014, 83, 45–51.
- Yokosuka, A. and Mimaki, Y., Phytochemistry, 2009, 70(6), 807–815.
- Da Silva, B. P., Valente, A. P. and Parente, J. P., Nat. Prod. Res., 2006, 20(04), 385–390.
- Jin, J. M., Liu, X. K. and Yang, C. R., J. Asian Nat. Prod. Res., 2003, 5(2), 95–103.
- Jin, J. M., Zhang, Y. J. and Yang, C. R., J. Nat. Prod., 2004, 67(1), 5–9.
- Mandal, D., Banerjee, S., Mondal, N. B., Chakravarty, A. K. and Sahu, N. P., Phytochemistry, 2006, 67(13), 1316–1321.
- Sharma, U., Saini, R., Kumar, N. and Singh, B., Chem. Pharm. Bull., 2009, 57(8), 890–893.
- Zhang, Y., Yang, C. R. and Zhang, Y. J., Helv. Chim. Acta, 2013, 96(9), 1807–1813.
- Guo-Lei, Z. H. U., Qian, H. A. O., RongTao, L. I. and Hai-Zhou, L. I., Chin. J. Nat. Med., 2014, 12(3), 213–217.
- Zhou, W. B. et al., J. Asian Nat. Prod. Res., 2010, 12(11), 955–961.
- Yokosuka, A., Jitsuno, M., Yui, S., Yamazaki, M. and Mimaki, Y., J. Nat. Prod., 2009, 72(8), 1399–1404.
Abstract Views: 414
PDF Views: 122