Novel daidzein analogs and their in vitro anti-influenza activities

Chemistry and Biodiversity

Volumn 12, Issue 4, 2015, Pages 685-696

  Chung, Shu Ting ^a   Huang, Yi Ting ^a   Hsiung, Hsin Yi ^a   Huang, Wen Hsin ^a   Yao, Chen Wen ^b   Lee, An Rong ^a  

^a NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^b TRI SERVICE GENERAL HOSPITAL   (Taiwan)

Author keywords

Anti influenza virus; Daidzein; H1N1 Tamiflu resistant virus; Isoflavonoids

Indexed keywords

2 [[3 (1,3 BENZODIOXOL 5 YL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 2 [[3 (4 BROMOPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 2 [[3 (4 CHLOROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 2 [[3 (4 FLUOROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 2 [[3 (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETIC ACID; 2 [[3 (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 2 [[3 (4 NITROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY}ACETONITRILE; 2 [[4 OXO 3 (3,4,5 TRIMETHOXYPHENYL) 4H 1 BENZOPYRAN 7 YL]OXY]ACETIC ACID; 2 [[4 OXO 3 (3,4,5 TRIMETHOXYPHENYL) 4H 1 BENZOPYRAN 7 YL]OXY]ACETONITRILE; 3 (1,3 BENZODIOXOL 5 YL) 7 HYDROXY 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 3 (4 BROMOPHENYL) 7 HYDROXY 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 3 (4 CHLOROPHENYL) 7 HYDROXY 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 3 (4 FLUOROPHENYL) 7 HYDROXY 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 7 HYDROXY 3 (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 7 HYDROXY 3 (4 NITROPHENYL) 4 OXO 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; 7 HYDROXY 4 OXO 3 (3,4,5 TRIMETHOXYPHENYL) 4H 1 BENZOPYRAN 8 CARBOXALDEHYDE; ANTIVIRUS AGENT; DAIDZEIN; ETHYL 2 [[3 (4 BROMOPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; ETHYL 2 [[3 (4 CHLOROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; ETHYL 2 [[3 (4 FLUOROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; ETHYL 2 [[3 (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; ETHYL 2 [[3 (4 NITROPHENYL) 4 OXO 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; ETHYL 2 [[4 OXO 3 (3,4,5 TRIMETHOXYPHENYL) 4H 1 BENZOPYRAN 7 YL]OXY]ACETATE; FLAVONOID; FORMONONENTIN; ISOFLAVONOID; OSELTAMIVIR; RIBAVIRIN; UNCLASSIFIED DRUG; UNINDEXED DRUG; ISOFLAVONE DERIVATIVE;

ANTIINFLUENZA ACTIVITY; ANTIVIRAL ACTIVITY; ANTIVIRAL RESISTANCE; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; INFLUENZA VIRUS A H1N1; MDCK CELL LINE; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; ANIMAL; CHEMICAL STRUCTURE; CHEMISTRY; DOG; DRUG EFFECTS; INFLUENZA A VIRUS (H1N1); PRECLINICAL STUDY; PROCEDURES; SYNTHESIS; VIROLOGY;

ORTHOMYXOVIRIDAE;

ANIMALS; ANTIVIRAL AGENTS; CHEMISTRY TECHNIQUES, SYNTHETIC; DOGS; DRUG EVALUATION, PRECLINICAL; DRUG RESISTANCE, VIRAL; INFLUENZA A VIRUS, H1N1 SUBTYPE; ISOFLAVONES; MADIN DARBY CANINE KIDNEY CELLS; MOLECULAR STRUCTURE; OSELTAMIVIR; RIBAVIRIN; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84927750935     PISSN: 16121872     EISSN: 16121880     Source Type: Journal    
DOI: 10.1002/cbdv.201400337     Document Type: Article

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