SYNTHESIS AND PHARMACOLOGICAL EVALUTION OF PYRAZOLO BENZOHIAZOLES AND THIAZOLIDINE DERIVATIVATES
2
Author(s):
S.K.SHARMA . R,S.V.MURALIMOHAN RAO
Vol - 4, Issue- 1 ,
Page(s) : 312 - 334
(2013 )
DOI : https://doi.org/10.32804/IRJMST
Abstract
Synthesis and pharmacological evaluation and characterization of thiazolidine derivatives asanti
hyperglycemic agents. The chemistry of these systems involves considerable biological interest as Thiazolidin-4-one nucleus has many pharmacological properties.that thiazolidin-4-ones derivativesexhibited potent anti-HIV, analgesic, anti-tubercular, anti-histaminic, anti-viral, hypoglycemic, anti-hyperlipidemic, anti-Inflammatory and CNS activities.
- Eicher, T.; Hauptmann, S. (2nd ed. 2003). The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications. Wiley-VCH.
- Tan et al., 2006.
- Review article (properties, biological activities, syntheses of pyrazoles): A. Schmidt, A.Dreger (2011). "Recent Advances in the Chemistry of Pyrazoles. Properties, ".
- Fowden; Noe, Ridd and White, (1959). Proc. Chem. SOC. 131.
- T. E. Gilchrist "Heterocyclic Chemistry" 3rd Edition, Longman, 1992.
- International Journal of Natural Product Science 2012; Spl Issue 1: 247.
- Tweit, R. C., J. Chem. Soc., 1970, 687.
- Rawal, R. K., Srivastava, T., Haq, W., Katti, S. B., J. Chem. Res., 368 (2004).
- Yadav, R., Srivastava, S. D., Srivastava, S.K., Ind.J. Chem44B: 1262-1266 (2005).
- Kidwai, M., Negi, N., Misra, P., J. Ind. Chem. Soc., 77: 46-47 (2000).
- Kidwai, M., Negi, N., Misra, P., J. Ind. Chem. Soc., 77: 46-47 (2000).Srivastava, V. K., Palit,
- G., et al, J. Indian Chem. Soc., 67: 335- 338 (1990).
- Amato.A.A.,Neves.F.A., 2012. Idealized PPARgamma-Based Therapies: Lessons from Bench and Bedside. PPAR Res., (2012).
- Shinkai.H, et al., Isoxazolidine-3,5-dione and Noncyclic 1,3-Dicarbonyl Compounds as
- Hypoglycemic Agents, J. Med. Chem. (1998), 41, 1927-1933.
- Sriram, D., Yogeeswari, P., Ashok kumar T. G., J. Indian Pharm. Sci., 67(4): 496-499, (2005).
- Omaima Mohamed AbdElhafez et al., Arch. Pharm. Res., 26(8):686-696 (2003).
|