SCOPUS 정보 검색 플랫폼

ChemMedChem

Volumn 9, Issue 3, 2014, Pages 627-637

Discovery of potent HDAC inhibitors based on chlamydocin with inhibitory effects on cell migration

(5) Wang, Shimiao a Li, Xiaohui a Wei, Yingdong a Xiu, Zhilong a Nishino, Norikazu b

a DALIAN UNIVERSITY OF TECHNOLOGY (China)

b KYUSHU INSTITUTE OF TECHNOLOGY (Japan)

Author keywords

cell migration; chlamydocin analogues; cyclic tetrapeptides; docking; HDAC inhibitors

Indexed keywords

CHLAMYDOCIN DERIVATIVE; GELATINASE A; HISTONE DEACETYLASE 4; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID DERIVATIVE; KY 2; PROTEIN P21; TISSUE INHIBITOR OF METALLOPROTEINASE 1; TRICHOSTATIN A; UNCLASSIFIED DRUG;

ANTIPROLIFERATIVE ACTIVITY; APOPTOSIS; ARTICLE; BINDING SITE; CELL CYCLE ARREST; CELL DEATH; CELL MIGRATION; CONTROLLED STUDY; DRUG DESIGN; ENZYME ACTIVITY; HUMAN; HUMAN CELL; HYDROPHOBICITY; MIGRATION INHIBITION; MOLECULAR DOCKING; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DOMAIN; PROTEIN MODIFICATION; SUBSTITUTION REACTION; WESTERN BLOTTING;

CELL MIGRATION; CHLAMYDOCIN ANALOGUES; CYCLIC TETRAPEPTIDES; DOCKING; HDAC INHIBITORS;

ANTINEOPLASTIC AGENTS; APOPTOSIS; CELL CYCLE; CELL MOVEMENT; CELL PROLIFERATION; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG DISCOVERY; DRUG SCREENING ASSAYS, ANTITUMOR; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; HUMANS; ISOENZYMES; K562 CELLS; MCF-7 CELLS; MOLECULAR STRUCTURE; PEPTIDES, CYCLIC; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84896727846 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.201300372 Document Type: Article

Times cited : (16)

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