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Volumn 44, Issue 5, 2009, Pages 1900-1912
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Design, synthesis, and evaluation of biphenyl-4-yl-acrylohydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors
c
Sigma Tau SpA
(Italy)
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Author keywords
Antiproliferative activity; Histone deacetylase; Synthesis
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Indexed keywords
5 (BIPHENYL 4 YL)PENTANOIC ACID N HYDROXYAMIDE;
5 BIPHENYL 4 YL PENTA 2,4 DIENOIC ACID N HYDROXYAMIDE;
ALPHA TUBULIN;
HISTONE DEACETYLASE 2;
HISTONE DEACETYLASE INHIBITOR;
ISOENZYME;
N HYDROXY 3 (4' CYANOBIPHENYL 4 YL)ACRYLAMIDE;
N HYDROXY 3 (4' HYDROXYBIPHENYL 4 YL)ACRYLAMIDE;
N HYDROXY 3 (4' HYDROXYBIPHENYL 4 YL)PROPIONAMIDE;
N HYDROXY 3 (4' METHOXYBIPHENYL 4 YL)ACRYLAMIDE;
N HYDROXY 3 [4 (4 HYDROXYPHENYL)CYCLOHEXYL]ACRYLAMIDE;
N HYDROXY 3 [4 (4 HYDROXYPHENYL)CYCLOHEXYL]PROPIONAMIDE;
N HYDROXY 3 [4' HYDROXYBIPHENYL 3 YL]ACRYLAMIDE;
N HYDROXY 3 [4' HYDROXYMETHYLBIPHENYL 4 YL]ACRYLAMIDE;
PROTEIN P53;
UNCLASSIFIED DRUG;
VORINOSTAT;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
COLON CARCINOMA;
CONTROLLED STUDY;
DRUG ACETYLATION;
DRUG BINDING SITE;
DRUG DESIGN;
DRUG SCREENING;
DRUG SYNTHESIS;
DRUG TOLERABILITY;
FEMALE;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
LUNG CARCINOMA;
MOLECULAR DOCKING;
MOUSE;
NONHUMAN;
OVARY CARCINOMA;
ACETYLATION;
APOPTOSIS;
BINDING SITES;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DRUG DESIGN;
ENZYME INHIBITORS;
FEMALE;
HISTONE DEACETYLASES;
HUMANS;
HYDROXAMIC ACIDS;
OVARIAN NEOPLASMS;
PROTEIN BINDING;
TUBULIN;
TUMOR SUPPRESSOR PROTEIN P53;
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EID: 62749154929
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2008.11.005 Document Type: Article |
Times cited : (71)
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References (36)
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