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Bioorganic and Medicinal Chemistry Letters

Volumn 22, Issue 8, 2012, Pages 2872-2876

Design, synthesis, synergistic antimicrobial activity and cytotoxicity of 4-aryl substituted 3,4-dihydropyrimidinones of curcumin

(4) Lal, Jaggi a Gupta, S K a Thavaselvam, D b Agarwal, D D a

a JIWAJI UNIVERSITY (India)

b DEFENCE RESEARCH AND DEVELOPMENT ESTABLISHMENT (India)

Author keywords

3,4 Dihydropyrimidinone analogues of curcumin; Cytotoxicity; IC 50; MIC; Zone of inhibition

Indexed keywords

3,4 DIHYDROPYRIMIDINONE DERIVATIVE; AMPICILLIN; ANTIINFECTIVE AGENT; CURCUMIN; CURCUMIN DERIVATIVE; CYTOTOXIC AGENT; DOXORUBICIN; FLUCONAZOLE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; ASPERGILLUS; BURKHOLDERIA PSEUDOMALLEI; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; COLON CARCINOMA; CONTROLLED STUDY; CURCUMA LONGA; CURVULARIA LUNATA; DRUG CYTOTOXICITY; DRUG DESIGN; DRUG SYNTHESIS; ESCHERICHIA COLI; FUNGUS; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; HUMAN; HUMAN CELL; IN VITRO STUDY; INFRARED SPECTROSCOPY; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; PSEUDOMONAS AERUGINOSA; SALMONELLA TYPHI; STAPHYLOCOCCUS AUREUS; TRICHODERMA VIRIDE;

ANTI-INFECTIVE AGENTS; ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL SURVIVAL; CURCUMIN; DRUG DESIGN; HUMANS; INHIBITORY CONCENTRATION 50; MICROBIAL SENSITIVITY TESTS; NEOPLASMS; PYRIMIDINONES;

FUNGI;

EID: 84862782023 PISSN: 0960894X EISSN: 14643405 Source Type: Journal
DOI: 10.1016/j.bmcl.2012.02.056 Document Type: Article

Times cited : (70)

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