cheminform abstract: synthesis, spectral characterization, and biological activity of some new...

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ChemInform 2010, 41, issue 41 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Phenothiazine derivatives R 0630 DOI: 10.1002/chin.201041166 Synthesis, Spectral Characterization, and Biological Activity of Some New Sub- stituted 10H-Phenothiazines, Its Ribofuranosides, and Sulfones. — The title com- pounds (IIa), (IIIa), (Va), and (VIII) exhibit strong radical scavenging activity in the DPPH assay. (IIa) and (IIIa) also show good antibacterial activity against Coagulase negative staphylococci strain. (VIII) shows good results against Candida albicans. — (GAUTAM, N.; AJMERA*, N.; GUPTA, S.; GAUTAM, D. C.; Nucleosides, Nucleotides Nucleic Acids 29 (2010) 3, 178-189, DOI:10.1080/15257771003708538 ; Dep. Chem., Univ. Rajasthan, Jaipur 302 055, India; Eng.) — K. Woydowski 41- 166

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Page 1: ChemInform Abstract: Synthesis, Spectral Characterization, and Biological Activity of Some New Substituted 10H-Phenothiazines, Its Ribofuranosides, and Sulfones

www.cheminform.wiley-vch.de

Phenothiazine derivativesR 0630 DOI: 10.1002/chin.201041166

Synthesis, Spectral Characterization, and Biological Activity of Some New Sub-stituted 10H-Phenothiazines, Its Ribofuranosides, and Sulfones. — The title com-pounds (IIa), (IIIa), (Va), and (VIII) exhibit strong radical scavenging activity in the DPPH assay. (IIa) and (IIIa) also show good antibacterial activity against Coagulase negative staphylococci strain. (VIII) shows good results against Candida albicans. — (GAUTAM, N.; AJMERA*, N.; GUPTA, S.; GAUTAM, D. C.; Nucleosides, Nucleotides Nucleic Acids 29 (2010) 3, 178-189, DOI:10.1080/15257771003708538 ; Dep. Chem., Univ. Rajasthan, Jaipur 302 055, India; Eng.) — K. Woydowski

41- 166

ChemInform 2010, 41, issue 41 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim