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Volumn 280, Issue 15, 2013, Pages 3563-3575

PARP inhibitors: Polypharmacology versus selective inhibition

Author keywords

ADP ribosyltransferases; cancer; drug design; PARP; poly(ADP ribose) polymerases; polypharmacology; promiscuity; selective inhibitors; selectivity; structure based drug design

Indexed keywords

AG 0 14699; ANTINEOPLASTIC AGENT; AZD 2461; BMN 673; BRCA1 PROTEIN; CAMPTOTHECIN; CEP 8983; CEP 9722; CISPLATIN; E 7016; E 7449; G 007LK; GEMCITABINE; GPI 21016; INIPARIB; INO 1001; IWR 2; LT 673; MULTIDRUG RESISTANCE PROTEIN; N (5,6 DIHYDRO 6 OXO 2 PHENANTHRIDINYL) 2 DIMETHYLAMINOACETAMIDE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 2; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE INHIBITOR; NIRAPARIB; OLAPARIB; RUCAPARIB; TEMOZOLOMIDE; UNCLASSIFIED DRUG; VELIPARIB; XAV 939;

EID: 84880329307     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/febs.12298     Document Type: Review
Times cited : (69)

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