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Volumn 25, Issue 19, 2015, Pages 4097-4103
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Catechols and 3-hydroxypyridones as inhibitors of the DNA repair complex ERCC1-XPF
a a a a a a a a a a a b a |
Author keywords
3 Hydroxypyridone; Catechol; Cisplatin potentiation; DNA repair; ERCC1 XPF
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Indexed keywords
3 HYDROXYPYRIDONE DERIVATIVE;
CATECHOL DERIVATIVE;
CISPLATIN;
DEOXYRIBONUCLEASE I;
DNA BINDING PROTEIN;
EXCISION REPAIR CROSS COMPLEMENTING PROTEIN 1;
HISTONE H2AX;
PYRIDONE DERIVATIVE;
UNCLASSIFIED DRUG;
XERODERMA PIGMENTOSUM GROUP F PROTEIN;
ENDONUCLEASE;
ERCC1 PROTEIN, HUMAN;
FEN1 PROTEIN, HUMAN;
FLAP ENDONUCLEASE;
ARTICLE;
DNA REPAIR;
DRUG POTENCY;
EXCISION REPAIR;
HIGH THROUGHPUT SCREENING;
HUMAN;
HUMAN CELL;
IC50;
MELANOMA;
STRUCTURE ACTIVITY RELATION;
ANTAGONISTS AND INHIBITORS;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
METABOLISM;
TUMOR CELL LINE;
CATECHOLS;
CELL LINE, TUMOR;
DEOXYRIBONUCLEASE I;
DNA REPAIR;
DNA-BINDING PROTEINS;
DOSE-RESPONSE RELATIONSHIP, DRUG;
ENDONUCLEASES;
FLAP ENDONUCLEASES;
HUMANS;
MOLECULAR STRUCTURE;
PYRIDONES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84945480180
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2015.08.031 Document Type: Article |
Times cited : (26)
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References (8)
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