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Volumn 15, Issue 10, 2007, Pages 3356-3367

Synthetic chalcones, flavanones, and flavones as antitumoral agents: Biological evaluation and structure-activity relationships

Author keywords

Antitumoral; Comet assay; Flavonoids; QSAR

Indexed keywords

1 (2 HYDROXYPHENYL) 3 (2 PYRIDINYL) 2 PROPEN 1 ONE; 1 (2 HYDROXYPHENYL) 3 (4 BENZYLOXYPHENYL) 1 PROPANONE; 1 (2 HYDROXYPHENYL) 3 (4 METHYLTHIOPHENYL) 2 PROPEN 1 ONE; 1 (2 HYDROXYPHENYL) 3 (4 NONYLOXYPHENYL) 2 PROPEN 1 ONE; 1 (2 HYDROXYPHENYL) 5 PHENYL 2,4 PENTADIEN 1 ONE; 1 (4 BENZYLOXY 2 HYDROXYPHENYL) 3 (2 BROMOPHENYL) 2 PROPEN 1 ONE; 1 (4 BUTOXY 2 HYDROXYPHENYL) 3 (4 BUTOXYPHENYL) 2 PROPEN 1 ONE; 2 (2 BROMOPHENYL) 4H CHROMEN 4 ONE; 2 (4 BROMOPHENYL) 2,3 DIHYDROCHROMEN 4 ONE; 2 (4 CHLOROPHENYL) 4H CHROMEN 4 ONE; 3 (2 BROMOPHENYL) 1 (2 HYDROXY 4,6 DIMETHOXYPHENYL) 2 PROPEN 1 ONE; 3 (2 BROMOPHENYL) 1 (2 HYDROXYPHENYL)PROP 2 EN 1 ONE; 3 (2 BROMOPHENYL) 1 PHENYL 2 PROPEN 1 ONE; 3 (4 AMINOPHENYL) 1 (2 HYDROXYPHENYL) 2 PROPEN 1 ONE; 3 (4 BENZYLOXY 3 IODOPHENYL) 1 (2 HYDROXYPHENYL) 2 PROPEN 1 ONE; 3 (4 BROMOPHENYL) 1 PHENYL 2 PROPEN 1 ONE; 3 (4 CHLOROPHENYL) 1 (2 HYDROXYPHENYL)PROP 2 EN 1 ONE; 3 (4 CHLOROPHENYL) 1 PHENYL 2 PROPEN 1 ONE; 3 (4 HEXYLOXYPHENYL) 1 (2 HYDROXYPHENYL) 2 PROPEN 1 ONE; 3 (4 METHOXYPHENYL) 1 PHENYL 2 PROPEN 1 ONE; 3 (4 METHYLTHIOPHENYL) 1 PHENYL 2 PROPEN 1 ONE; 3 HYDROXY 1 (2 HYDROXYPHENYL) 3 (4 METHYLTHIOPHENYL) 1 PROPANONE; ANTINEOPLASTIC AGENT; CHALCONE; FLAVANONE; FLAVONE; N [4 (3 OXO 3 PHENYL 1 PROPENYL)PHENYL]ACETAMIDE; N [4 [3 (2 HYDROXYPHENYL) 3 OXO 1 PROPENYL]PHENYL]ACETAMIDE; UNCLASSIFIED DRUG;

EID: 34047185373     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2007.03.031     Document Type: Article
Times cited : (299)

References (72)
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    • In derivative 44 the phenyl C-C distances in the range from 1.371(6) to 1.410(6) Å correspond to formally resonant C-C bonds. Single C1-C2 and C2-C3 bond lengths in the fused chromane cycle are 1.519(6) and 1.504(6) Å, respectively. π-delocalization at the C3-C4 bond leads to a slightly shorter C-C distance of 1.480(6) Å. Similarly, π-delocalization at the O1-C9 bond makes the O1-C9 length slightly shorter than the O1-C1 distance (1.367(5) and 1.452(5) Å, respectively). The phenyl rings are tilted to each other subtending a dihedral angle of 57.0(2)° (atomic coordinates, bond distances and angles, crystal data, data collection procedure, structure determination method, and refinement results are given as Supplementary information).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.