Indexed keywords
2 AMINO 4 (5 CHLORO 1 (4 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL) 5 OXO 1 (PYRAZOL 4 YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
2 AMINO 4 (5 CHLORO 1 (4 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
2 AMINO 4 (5 CHLORO 3 METHYL 1 4 TOLYL 1H PYRAZOL 4 YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
2 AMINO 4 (5 CHLORO 3 METHYL 1 4 TOLYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE;
ANTIINFECTIVE AGENT;
ANTINEOPLASTIC AGENT;
EPIDERMAL GROWTH FACTOR RECEPTOR;
ETHYL 2 AMINO 4 (5 CHLORO 1 (4 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
ETHYL 2 AMINO 4 (5 CHLORO 1 (4 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
ETHYL 2 AMINO 4 (5 CHLORO 3 METHYL 1 4 TOLYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
ETHYL 2 AMINO 4 (5 CHLORO 3 METHYL 1 4 TOLYL 1H PYRAZOL 4YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
ETHYL 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
ETHYL 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4YL) 5 OXO 1 (PYRIDIN 3 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBOXYLATE;
PYRAZOLE DERIVATIVE;
PYRIDINE DERIVATIVE;
QUINOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTIBACTERIAL ACTIVITY;
ANTINEOPLASTIC ACTIVITY;
ANTIPROLIFERATIVE ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CELL PROLIFERATION ASSAY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
ESCHERICHIA COLI;
HYDROGEN BOND;
MINIMUM INHIBITORY CONCENTRATION;
MOLECULAR DOCKING;
MOLECULAR HYBRIDIZATION;
MOLECULAR MODEL;
PROTON NUCLEAR MAGNETIC RESONANCE;
ANTAGONISTS AND INHIBITORS;
CELL PROLIFERATION;
CHEMISTRY;
DRUG EFFECTS;
HUMAN;
IC50;
MASS SPECTROMETRY;
MICROBIAL SENSITIVITY TEST;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TUMOR CELL LINE;
ANTI-BACTERIAL AGENTS;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
HUMANS;
INHIBITORY CONCENTRATION 50;
MAGNETIC RESONANCE SPECTROSCOPY;
MASS SPECTROMETRY;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR DOCKING SIMULATION;
PYRAZOLES;
PYRIDINES;
QUINOLINES;
RECEPTOR, EPIDERMAL GROWTH FACTOR;
STRUCTURE-ACTIVITY RELATIONSHIP;
3
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