Syntheses and Antimicrobial Activities of 4-Aryl-5-phenylimino-3-S-(hepta-O-acetyl lactosyl)-1,2,4-thiadiazolines

Autor:	Shirish P. Deshmukh, Dattatraya V. Mangte
Rok vydání:	2007
Předmět:	chemistry.chemical_compound chemistry Elemental analysis Aryl Heteroatom medicine Organic chemistry General Chemistry General Medicine Candida guilliermondii Antimicrobial Chloride medicine.drug
Zdroj:	ChemInform. 38
ISSN:	1522-2667 0931-7597
DOI:	10.1002/chin.200738130
Popis:	A series of 4-aryl-5-phenylimino-3-S-(hepta-O-acetyl lactosyl)-1,2,4-thiadiazolines have been synthesized by the interaction of S-(hepta-O-acetyl lactosyl)-1-arylisothiocarbamides and S-chloro-N-phenyl isothiocarbamoyl chloride. The title compounds were characterized on the basis of elemental analysis and IR, NMR, mass spectral studies. The title compounds exhibited comparable antimicrobial activities against pathogens such as E. coli, S. aureus, P. vulgaris, S. typhi, A. niger, and Candida guilliermondii. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:390–392, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20310
Databáze:	OpenAIRE
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