SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 3, 2014, Pages 657-664

Design, synthesis, and biological activity of NCC149 derivatives as histone deacetylasea 8-selective inhibitors

(11) Suzuki, Takayoshi a,b Muto, Nobusuke c Bando, Masashige d Itoh, Yukihiro a Masaki, Ayako e Ri, Masaki e Ota, Yosuke a Nakagawa, Hidehiko c Iida, Shinsuke e Shirahige, Katsuhiko d Miyata, Naoki c

a KYOTO PREFECTURAL UNIVERSITY OF MEDICINE (Japan)

b JAPAN SCIENCE AND TECHNOLOGY AGENCY (Japan)

c NAGOYA CITY UNIVERSITY (Japan)

d UNIVERSITY OF TOKYO (Japan)

e NAGOYA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCES (Japan)

Author keywords

anticancer agents; histone deacetylase; inhibitors; isozyme selectivity; T cell lymphomas

Indexed keywords

2 (PHENYLTHIO) N HYDROXYETHANIMIDAMIDE; 2 (PHENYLTHIO)ACETAMIDE; 2 (PHENYLTHIO)ETHANETHIOAMIDE; 3 (3 BROMOMETHYLPHENYL)BENZOIC ACID METHYL ESTER; 3 (3 HYDROXYMETHYLPHENYL)BENZOIC ACID METHYL ESTER; 3 (3 PHENYLTHIOMETHYLPHENYL) N (TETRAHYDROPYRAN 2 YLOXY)BENZAMIDE; 3 (3 PHENYLTHIOMETHYLPHENYL) N HYDROXYBENZAMIDE; 3 (3 PHENYLTHIOMETHYLPHENYL)BENZOIC ACID; 3 (3 PHENYLTHIOMETHYLPHENYL)BENZOIC ACID METHYL ESTER; 3 (5 BROMOMETHYLTHIOPHEN 2 YL)BENZOIC ACID METHYL ESTER; 3 (5 METHYLTHIOPHEN 2 YL)BENZOIC ACID METHYL ESTER; 3 (5 PHENYLTHIOMETHYLTHIOPHEN 2 YL) N HYDROXYBENZAMIDE; 3 [2 (PHENYLTHIOMETHYL)THIAZOL 4 YL] N HYDROXYBENZAMIDE; 3 [2 (PHENYLTHIOMETHYL)THIAZOL 4 YL]BENZOIC ACID METHYL ESTER; 3 [3 (PHENYLTHIOMETHYL) 1,2,4 OXADIAZOL 5 YL] N HYDROXYBENZAMIDE; 3 [3 (PHENYLTHIOMETHYL) 1,2,4 OXADIAZOL 5 YL]BENZOIC ACID METHYL ESTER; 3 [4 (PHENYLTHIOMETHYL) 1H 1,2,3 TRIAZOL 1 YL] N HYDROXYBENZAMIDE; 3 [4 (PHENYLTHIOMETHYL) 1H 1,2,3 TRIAZOL 1 YL]BENZOIC ACID ETHYL ESTER; 3 ACETYLBENZOIC ACID METHYL ESTER; 3 AZIDO BENZOIC ACID ETHYL ESTER; ALPHA BROMO 3 ACETYLBENZOIC ACID METHYL ESTER; ALPHA TUBULIN; ANTINEOPLASTIC AGENT; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE 8; HISTONE DEACETYLASE INHIBITOR; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; COMPETITIVE INHIBITION; CONTROLLED STUDY; DRUG ACETYLATION; DRUG DESIGN; DRUG DETERMINATION; DRUG PURITY; DRUG SCREENING; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; FEMALE; HUMAN; HUMAN CELL; IN VITRO STUDY; PRIORITY JOURNAL; T CELL LYMPHOMA;

ANTICANCER AGENTS; HISTONE DEACETYLASE; INHIBITORS; ISOZYME SELECTIVITY; T-CELL LYMPHOMAS;

ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL PROLIFERATION; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG DESIGN; DRUG SCREENING ASSAYS, ANTITUMOR; HELA CELLS; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; HUMANS; HYDROXAMIC ACIDS; MOLECULAR STRUCTURE; REPRESSOR PROTEINS; STRUCTURE-ACTIVITY RELATIONSHIP; TRIAZOLES;

EID: 84896738946 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.201300414 Document Type: Article

Times cited : (63)

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