Synthesis of feruloyl-myo-insitol derivatives and their inhibitory effects on phorbol ester-induced superoxide generation and Esptein-Barr virus activation

Bioorganic and Medicinal Chemistry

Volumn 10, Issue 6, 2002, Pages 1855-1863

  Hosoda, Asao ^a   Nomura, Eisaku ^a   Murakami, Akira ^b   Koshimizu, Koichi ^b   Ohigashi, Hajime ^c   Mizuno, Kazuhiko ^d   Taniguchi, Hisaji ^a  

^a INDUSTRIAL TECHNOLOGY CENTER OF WAKAYAMA PREFECTURE   (Japan)

^b KINKI UNIVERSITY   (Japan)

^c KYOTO UNIVERSITY   (Japan)

^d Osaka Prefecture University   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 O BIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 1,2,4,5 TETRA O ACETYL 3,6 O BIS[3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 1,2:4,5 DI O CYCLOHEXYLIDENE 3,6 O BIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 1,3,4,5,6 PENTA O ACETYL 2 O [3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 1,6 O BIS[3 (4' ACETYLOXY 3' METHOXYPHENYL) 2 PROPENOYL] 3,4 O (1,1,3,3 TETRAISOPROPYLDISILOXANEDI 1,3 YL)INOSITOL; 1,6 O BIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 2,3,4,5 TETRA O ACETYL 1,6 O BIS[3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 2,4,6 O TRIS[3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL 1,3,5 (2 FORMATE); 2,4,6 O TRIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL 1,3,5 (2 FORMATE); 3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL CHLORIDE; 3,4,5,6 TETRA O ACETYL 1,2 O BIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 3,4,5,6 TETRA O ACETYLINOSITOL; 3,6 O BIS[3 (4' ACETOXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; 3,6 O BIS[3 (4' HYDROXY 3' METHOXYPHENYL) 2 PROPENOYL]INOSITOL; ANTINEOPLASTIC AGENT; INOSITOL DERIVATIVE; PHORBOL 13 ACETATE 12 MYRISTATE; SUPEROXIDE; UNCLASSIFIED DRUG; DRUG DERIVATIVE; INOSITOL; PHORBOL ESTER; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ANTINEOPLASTIC ACTIVITY; ANTIVIRAL ACTIVITY; ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG EFFECT; DRUG STRUCTURE; DRUG SYNTHESIS; EPSTEIN BARR VIRUS; HUMAN; HUMAN CELL; HYDROPHOBICITY; STEREOCHEMISTRY; VIRUS ACTIVATION; VIRUS INHIBITION; CELL LINE; CELL STRAIN HL 60; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PHYSIOLOGY; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

HUMAN HERPESVIRUS 4;

CELL LINE; HERPESVIRUS 4, HUMAN; HL-60 CELLS; HUMANS; INOSITOL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; NADPH OXIDASE; PHORBOL ESTERS; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; SUPEROXIDES; VIRUS ACTIVATION;

EID: 0036009882     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00010-X     Document Type: Article

References (17)