Effects of positional and geometrical isomerism on the biological activity of some novel oxazolidinones
…, M Roshaiah, PG Sankar, A Khadeer, MS Kumar…
Index: Das, Jagattaran; Rao, C.V. Laxman; Sastry; Roshaiah; Sankar, P. Gowri; Khadeer, Abdul; Kumar, M. Sitaram; Mallik, Arundhuti; Selvakumar; Iqbal, Javed; Trehan, Sanjay Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 2 p. 337 - 343
Full Text: HTML
Citation Number: 26
Abstract
Some novel oxazolidinone derivatives with benzotriazole as pendant have been synthesized and tested for antibacterial activity. Linearly attached benzotriazole derivative showed more potency compared to angular one in vitro. Out of E/Z-isomers of angularly attached derivatives E-isomer was found to be more potent than Z-isomer. Either less active or inactive molecules were obtained, when benzotriazole was replaced with ...
Related Articles:
Reaction of 2-hetaryl-2-(tetrahydro-2-furanylidene) acetonitriles with aldehydes
[Khilya; Baglay; Volovenko Chemistry of Heterocyclic Compounds, 2010 , vol. 46, # 8 p. 934 - 937]
[Dekhane, Deepak V.; Pawar, Shivaji S.; Gupta, Sunil V.; Shingare, Murlidhar S.; Thore, Shivaji N. Chinese Chemical Letters, 2010 , vol. 21, # 5 p. 519 - 523]
[Fairley; Tidwell; Donkor; Naiman; Ohemeng; Lombardy; Bentley; Cory Journal of Medicinal Chemistry, 1993 , vol. 36, # 12 p. 1746 - 1753]