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Volumn 20, Issue 4, 2012, Pages 1482-1493
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Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, dihydro analogues and photo-dimers
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Author keywords
Malaria; Natural product; Photochemical dimerisation; Pyran 2 one; Tuberculosis
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Indexed keywords
11,12,11'12' TETRAMETHOXY ANIBA DIMER;
4 METHOXY 6 (3 (4 TERT BUTYL PHENOXY) STYRYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (3 NITROSTYRYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (3 PHENOXY STYRYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (4 (4 DIMETHYLAMINOPHENYL) 1,3 BUTADIENYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (4 NITROSTYRYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (4 PHENYL 1,3 BUTADIENYL) 2H PYRAN 2 ONE;
4 METHOXY 6 (4 TERT BUTYL STYRYL) 2H PYRAN 2 ONE;
4 METHOXY 6 [2 (1 NAPHTHYL)ETHENYL] 2H PYRAN 2 ONE;
4 METHOXY 6 [2 (1 NAPHTHYL)ETHYL]2H PYRAN 2 ONE;
4 METHOXY 6 [2 (2 FURYL)ETHENYL] 2H PYRAN 2 ONE;
4 METHOXY 6 [2 (2 NAPHTHYL)ETHENYL] 2H PYRAN 2 ONE;
4 METHOXY 6 [2 (2 NAPHTHYL)ETHYL]2H PYRAN 2 ONE;
4 METHOXY 6 [2 (4 TERT BUTYLPHENYL)ETHYL] 2H PYRAN 2 ONE;
4 METHOXY 6 STYRYL 2H PYRAN 2 ONE;
4 METHOXY 6 STYRYL PYRAN 2 ONE DERIVATIVE;
6 [2 (1,3 BENZODIOXO 5 YL)ETHENYL] 4 METHOXY 2H PYRAN 2 ONE;
6 [2 (1,3 BENZODIOXO 5 YL)ETHYL] 4 METHOXY 2H PYRAN 2 ONE;
6 [2 (3 (4 TERT BUTYLPHENOXY)PHENYL)ETHYL]2H PYRAN 2 ONE;
6 [2 (3,4 DIMEHOXYPHENYL)ETHENYL] 4 METHOXY 2H PYRAN 2 ONE;
6 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 4 METHOXY 2H PYRAN 2 ONE;
6,6' (2,2' (1,4 PHENYLENE)BIS(ETHANE 2,1 DIYL))BIS (4 METHOXY 2H PYRAN 2 ONE);
6,6' (2,4 BIS (3,4 DIMETHOXYPHENYL)CYCLOBUTANE 1,3 DIYL)BIS (4 METHOXY 2H PYRAN 2 ONE);
6,6' (3,4 DIPHENYLCYCLOBUTANE 1,2 DIYL)BIS (4 METHOXY 2H PYRAN 2 ONE);
6,6' 2,2' (1,4 PHENYLENE)BIS(ETHENE 2,1 DIYL)BIS (4 METHOXY 2H PYRAN 2 ONE);
7,8 DIHYDRO 4 METHOXY 6 STYRYL 2H PYRAN 2 ONE;
ANTIMALARIAL AGENT;
NATURAL PRODUCT;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ANTIMALARIAL ACTIVITY;
ANTIPROTOZOAL ACTIVITY;
ANTITUBERCULOSIS ACTIVITY;
ARTICLE;
CYCLOADDITION;
DIMERIZATION;
DRUG ACTIVITY;
DRUG CYTOTOXICITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
LEISHMANIA DONOVANI;
MASS SPECTROMETRY;
MINIMUM INHIBITORY CONCENTRATION;
MYCOBACTERIUM TUBERCULOSIS;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PHOTOCHEMISTRY;
PLASMODIUM FALCIPARUM;
STRUCTURE ACTIVITY RELATION;
THIN LAYER CHROMATOGRAPHY;
TRYPANOSOMA CRUZI;
TRYPANOSOMA RHODESIENSE;
ANTIMALARIALS;
ANTITUBERCULAR AGENTS;
COUMARINS;
DIMERIZATION;
FATTY ACIDS, MONOUNSATURATED;
INHIBITORY CONCENTRATION 50;
LEISHMANIA DONOVANI;
LIGHT;
MOLECULAR STRUCTURE;
PLASMODIUM FALCIPARUM;
PYRONES;
ANIBA;
LEISHMANIA DONOVANI;
MYCOBACTERIUM TUBERCULOSIS;
PLASMODIUM FALCIPARUM;
TRYPANOSOMA BRUCEI RHODESIENSE;
TRYPANOSOMA CRUZI;
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EID: 84857035404
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2011.12.053 Document Type: Article |
Times cited : (52)
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References (30)
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