|
Volumn 8, Issue 1, 2013, Pages 125-135
|
Synthesis and Quantitative Structure-Activity Relationships of Selective BCRP Inhibitors
|
Author keywords
ABC transporter; Antitumor agents; BCRP; Drug design; Inhibitors; QSAR
|
Indexed keywords
2 (3 AMINOBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (3 CHLOROBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (4 AMINOBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (4 CHLOROBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (4 CYANOBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (4 HYDROXYBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (4 TERT BUTYLBENZAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 (CYCLOHEXANCARBOXAMIDO) N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
2 ACETAMIDO N [4 (2 HYDROXYETHYL)PHENYL]BENZAMIDE;
4 [2 [4 (2 HYDROXYETHYL)PHENYLCARBAMOYL]PHENYLCARBAMOYL]PHENYL ACETATE;
4 CHLORO N [4 (2 HYDROXYETHYL)PHENYL] 2 (4 NITROBENZAMIDO)BENZAMIDE;
5 CHLORO N [4 (2 HYDROXYETHYL)PHENYL] 2 (4 NITROBENZAMIDO)BENZAMIDE;
ANTINEOPLASTIC AGENT;
BREAST CANCER RESISTANCE PROTEIN;
FIRTECAN;
MITOXANTRONE;
N [2 [4 (2 HYDROXYETHYL)PHENYLCARBAMOYL]PHENYL] 3,4 DIMETHOXYBENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 2 (3 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 2 (4 ISOPROPOXYBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 2 (4 METHYLBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 2 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 2 [4 (TRIFLUOROMETHYL)BENZAMIDO]BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 3 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 4 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 4 METHOXY 2 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 4 METHYL 2 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 4,5 DIMETHOXY 2 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 5 METHOXY 2 (4 NITROBENZAMIDO)BENZAMIDE;
N [4 (2 HYDROXYETHYL)PHENYL] 5 METHYL 2 (4 NITROBENZAMIDO)BENZAMIDE;
PROTEIN INHIBITOR;
UNCLASSIFIED DRUG;
ARTICLE;
BINDING SITE;
CANCER CELL;
CELL VIABILITY;
CYTOTOXICITY;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG PROTEIN BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
HYDROGEN BOND;
PRIORITY JOURNAL;
QUANTITATIVE STRUCTURE ACTIVITY RELATION;
SUBSTITUTION REACTION;
ANTINEOPLASTIC AGENTS;
ATP-BINDING CASSETTE TRANSPORTERS;
BREAST NEOPLASMS;
CELL LINE, TUMOR;
CELL SURVIVAL;
DRUG DESIGN;
DRUG RESISTANCE, MULTIPLE;
DRUG RESISTANCE, NEOPLASM;
FEMALE;
HUMANS;
MITOXANTRONE;
NEOPLASM PROTEINS;
P-GLYCOPROTEIN;
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP;
QUINOLINES;
|
EID: 84871668993
PISSN: 18607179
EISSN: 18607187
Source Type: Journal
DOI: 10.1002/cmdc.201200377 Document Type: Article |
Times cited : (32)
|
References (21)
|