Synthesis, stereochemistry and biological activity of some novel long alkyl chain substituted thiazolidin-4-ones and thiazan-4-one from 10-undecenoic acid hydrazide

European Journal of Medicinal Chemistry

Volumn 40, Issue 2, 2005, Pages 173-184

  Rahman, V P Mujeebur ^a   Mukhtar, Sayeed ^a   Ansari, Wajid Husain ^a   Lemiere, Guy ^b  

^a ALIGARH MUSLIM UNIVERSITY   (India)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Acylhydrazone; Antimicrobial activity; Cytotoxic activity; Terminal carboxymethyl ethylthio acylhydrazones; Tetrahydro 1,3 thiazin 4 one; Thiazolidin 4 ones

Indexed keywords

10 UNDECENOIC ACID; 2 [[11 [[5 METHYL 2 (3 NITROPHENYL) 4 OXO 1,3 THIAZOLIDIN 3 YL]AMINO] 11 OXOUNDECYL]SULFANYL]PROPANOIC ACID; 3 [[11 [2 (3 NITROBENZYLIDENE)HYDRAZINO] 11 OXOUNDECYL]SULFANYL]PROPANOIC ACID; 3 [[11 [[2 (3 NITROPHENYL) 4 OXO 1,3 THIAZINAN 3 YL]AMINO] 11 OXOUNDECENYL]SULFANYL]PROPANOIC ACID; 3 NITROBENZALDEHYDE 10 UNDECENOHYDRAZONE; [[11 [2 (3 NITROBENZYLIDENE)HYDRAZINO] 11 OXOUNDECYL]SULFANYL]ACETIC ACID; [[11 [[2 (3 NITROPHENYL) 4 OXO 1,3 THIAZOLIDIN 3 YL]AMINO] 11 OXOUNDECYL]SULFANYL]ACETIC ACID; ACETIC ACID DERIVATIVE; BENZALDEHYDE DERIVATIVE; CHLORAMPHENICOL; FLUCONAZOLE; HYDRAZIDE DERIVATIVE; N [5 METHYL 2 (3 NITROPHENYL) 4 OXO 1,3 THIAZOLIDIN 3 YL]UNDEC 10 ENAMIDE; PROPIONIC ACID DERIVATIVE; THIAZOLIDINE DERIVATIVE; THIOGLYCOLIC ACID; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTINEOPLASTIC ACTIVITY; ARTICLE; BIOASSAY; CARBON NUCLEAR MAGNETIC RESONANCE; CONTROLLED STUDY; CYTOTOXICITY TEST; DRUG SYNTHESIS; HUMAN; HUMAN CELL; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

ACETIC ACIDS; ANTI-INFECTIVE AGENTS; ANTINEOPLASTIC AGENTS; BACTERIA; BIOLOGICAL ASSAY; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; HYDRAZINES; HYDRAZONES; MICROBIAL SENSITIVITY TESTS; MODELS, CHEMICAL; NITROBENZENES; STEREOISOMERISM; SULFUR COMPOUNDS; THIAZOLES; TUMOR CELLS, CULTURED;

EID: 13444302530     PISSN: 02235234     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmech.2004.10.003     Document Type: Article

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