SCOPUS 정보 검색 플랫폼

Volumn 69, Issue , 2013, Pages 77-89

Design, synthesis, and structure-activity relationships of novel 6,7-disubstituted-4-phenoxyquinoline derivatives as potential antitumor agents

(6) Tang, Qidong a Zhao, Yanfang a Du, Xinming a Chong, Lian'E a Gong, Ping a Guo, Chun a

a SHENYANG PHARMACEUTICAL UNIVERSITY (China)

Author keywords

Antiproliferative activity; c Met; Quinoline derivatives; Synthesis

Indexed keywords

ANTINEOPLASTIC AGENT; FORETINIB; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 (2 FLUORPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 (2,4 DIMETHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 (4 FLUORPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 [4 (METHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 [4 (TRIFLUOROMETHYL)PHENYL]PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 O TOLYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 P TOLYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 (3 MORPHOLINOPROPOXY)QUINOLIN 4 XYLOXY]PHENYL] 4 PHENYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 (2 FLUOROPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 (2,4 DIMETHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 (4 FLUOROPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 (4 METHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 [4 (TRIFLUOROMETHYL)PHENYL]PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 O TOLYPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 P TOLYPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (4 METHYLPIPERAZIN 1 YL) PROPOXY]QUINOLIN 4 YLOXY]PHENYL] 4 PHENYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PIPERIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 (4 FLUOROPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PIPERIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 P TOLYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PIPERIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 PHENYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 (2,4 DIMETHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 (4 FLUOROPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 (4 METHOXYPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 (4,2 FLUOROPHENYL)PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 [4 (TRIFLUOROMETHYL)PHENYL]PICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 O TOLYLPICOLINAMIDE; N [3 FLUORO 4 [6 METHOXY 7 [3 (PYRROLIDIN 1 YL)PROPOXY] QUINOLIN 4 YLOXYL]PHENYL] 4 P TOLYLPICOLINAMIDE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTINEOPLASTIC ACTIVITY; ANTIPROLIFERATIVE ACTIVITY; ARTICLE; CANCER CELL CULTURE; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG DESIGN; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; STRUCTURE ACTIVITY RELATION;

ANTIPROLIFERATIVE ACTIVITY; C-MET; QUINOLINE DERIVATIVES; SYNTHESIS;

ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL PROLIFERATION; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG DESIGN; DRUG SCREENING ASSAYS, ANTITUMOR; ENZYME ACTIVATION; HT29 CELLS; HUMANS; MOLECULAR STRUCTURE; PROTEIN KINASE INHIBITORS; PROTO-ONCOGENE PROTEINS C-MET; QUINOLINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84883262213 PISSN: 02235234 EISSN: 17683254 Source Type: Journal
DOI: 10.1016/j.ejmech.2013.08.019 Document Type: Article

Times cited : (54)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.