SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 3, 2014, Pages 523-536

Towards selective inhibition of histone deacetylase isoforms: What has been achieved, where we are and what will be next

(2) Thaler, Florian a Mercurio, Ciro b

a EUROPEAN INSTITUTE OF ONCOLOGY (Italy)

b Genextra Group (Italy)

Author keywords

drug discovery; histone deacetylases; isoform selectivity; oncology; X ray crystallography

Indexed keywords

BORTEZOMIB; ENTINOSTAT; HISTONE DEACETYLASE; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 10; HISTONE DEACETYLASE 11; HISTONE DEACETYLASE 2; HISTONE DEACETYLASE 3; HISTONE DEACETYLASE 4; HISTONE DEACETYLASE 5; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE 7; HISTONE DEACETYLASE 8; HISTONE DEACETYLASE 9; HISTONE DEACETYLASE INHIBITOR; INTERLEUKIN 10; METHYL CPG BINDING PROTEIN 2; MOCETINOSTAT; OCTAMER TRANSCRIPTION FACTOR 4; PANOBINOSTAT; QUISINOSTAT; RICOLINOSTAT; ROMIDEPSIN; SILENCING MEDIATOR OF RETINOID AND THYROID HORMONE RECEPTOR; THALIDOMIDE; TUBACIN; UNCLASSIFIED DRUG; VORINOSTAT;

CANCER CELL; CARBONYLATION; CELL CYCLE REGULATION; CRYSTAL STRUCTURE; DNA DAMAGE; DRUG DESIGN; DRUG SCREENING; DRUG SYNTHESIS; ENZYME ACTIVITY; ENZYME INHIBITION; ENZYME PHOSPHORYLATION; HIGH THROUGHPUT SCREENING; HISTONE ACETYLATION; HUMAN; MOLECULAR MODEL; NITROSYLATION; NONHUMAN; PHASE 1 CLINICAL TRIAL (TOPIC); PRIORITY JOURNAL; PROTEIN PROCESSING; REVIEW; SUMOYLATION; X RAY CRYSTALLOGRAPHY;

DEPSIPEPTIDES; DRUG DISCOVERY; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; HUMANS; HYDROXAMIC ACIDS; ISOENZYMES; MOLECULAR STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84896703864 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.201300413 Document Type: Review

Times cited : (87)

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