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      KCI등재후보

      3D-QSAR Studies of 3,5-disubstituted Quinolines Inhibitors of c-Jun N-terminal Kinase-3 = 3D-QSAR Studies of 3,5-disubstituted Quinolines Inhibitors of c-Jun N-terminal Kinase-3

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      https://www.riss.kr/link?id=A105546466

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      다국어 초록 (Multilingual Abstract)

      c-Jun N-terminal kinase-3 (JNK-3) has been shown to mediate neuronal apoptosis and make the promising therapeutic target for neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and other CNS disorders. In order to better under...

      c-Jun N-terminal kinase-3 (JNK-3) has been shown to mediate neuronal apoptosis and make the promising therapeutic target for neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and other CNS disorders. In order to better understand the structural and chemical features of JNK-3, comparative molecular field analysis (CoMFA) was performed on a series of 3,5-disubstituted quinolines derivatives. The best predictions were obtained CoMFA model ($q^2$=0.707, $r^2$=0.972) and the statistical parameters from the generated 3D-QSAR models were indicated that the data are well fitted and have high predictive ability. The resulting contour map from 3D-QSAR models might be helpful to design novel and more potent JNK3 derivatives.

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      참고문헌 (Reference)

      1 Sybyl 8.1, "Tripos Inc., St. Louis, MO 63144, USA"

      2 M. A. Bogoyevitch, "The isoform-specific functions of the c- Jun N-terminal kinases (JNKs): differences revealed by gene targeting" 28 : 923-934, 2006

      3 A. M. Bode, "The functional contrariety of JNK" 46 : 591-598, 2007

      4 J. M. A. Siddiqui, "Small Molecule JNK (c-Jun N-Terminal Kinase) Inhibitors" 53 : 3005-3012, 2010

      5 R. J. Davis, "Signal transduction by the JNK group of MAP kinases" 103 : 239-252, 2000

      6 S. Gupta, "Selective interaction of JNK protein kinase isoforms with transcription factors" 15 : 2760-2770, 1996

      7 J. M. Kyriakis, "Pp54 microtubuleassociated protein 2 kinase" 265 : 17355-17363, 1990

      8 S. Wold, "PLSregression: a basic tool of chemometrics" 58 : 109-130, 2001

      9 J. M. Kyriakis, "Mammalian mitogen- activated protein kinase signal transduction pathways activated by stress and inflammation" 81 : 807-869, 2001

      10 M. Hibi, "Identification of an oncoprotein and UVresponsive protein kinase that binds and potentiates the c-Jun activation domain" 7 : 2135-2148, 1993

      1 Sybyl 8.1, "Tripos Inc., St. Louis, MO 63144, USA"

      2 M. A. Bogoyevitch, "The isoform-specific functions of the c- Jun N-terminal kinases (JNKs): differences revealed by gene targeting" 28 : 923-934, 2006

      3 A. M. Bode, "The functional contrariety of JNK" 46 : 591-598, 2007

      4 J. M. A. Siddiqui, "Small Molecule JNK (c-Jun N-Terminal Kinase) Inhibitors" 53 : 3005-3012, 2010

      5 R. J. Davis, "Signal transduction by the JNK group of MAP kinases" 103 : 239-252, 2000

      6 S. Gupta, "Selective interaction of JNK protein kinase isoforms with transcription factors" 15 : 2760-2770, 1996

      7 J. M. Kyriakis, "Pp54 microtubuleassociated protein 2 kinase" 265 : 17355-17363, 1990

      8 S. Wold, "PLSregression: a basic tool of chemometrics" 58 : 109-130, 2001

      9 J. M. Kyriakis, "Mammalian mitogen- activated protein kinase signal transduction pathways activated by stress and inflammation" 81 : 807-869, 2001

      10 M. Hibi, "Identification of an oncoprotein and UVresponsive protein kinase that binds and potentiates the c-Jun activation domain" 7 : 2135-2148, 1993

      11 J. H. Martin, "Developmental expression in the mouse nervous system of the p493F12 SAP kinase" 35 : 47-57, 1996

      12 C. Dong, "Defective T cell differentiation in the absence of Jnk1" 282 : 2092-2095, 1998

      13 S. J. Cho, "Cross-validated R2- guided region selection for comparative molecular field analysis: A simple method to achieve consistent results" 38 : 1060-1066, 1995

      14 R. D. Cramer, "Comparative molecular field analysis (CoMFA).1. Effect of shape on binding of steroids to carrier proteins" 110 : 5959-5967, 1988

      15 G. Y. Zhang, "Agents targeting c- Jun N-terminal kinase pathway as potential neuroprotectants" 14 : 1373-1383, 2005

      16 V. Adler, "Affinity-purified c-Jun amino-terminal protein kinase requires serine/threonine phosphorylation for activity" 267 : 17001-17005, 1992

      17 R. Jiang, "3,5-Disubstituted quinolines as novel c-Jun N-terminal kinase inhibitors" 17 : 6378-6382, 2007

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 신규평가 신청대상 (신규평가)
      2021-12-01 평가 등재후보 탈락 (계속평가)
      2020-12-01 평가 등재후보로 하락 (재인증) KCI등재후보
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2013-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2012-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2010-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.45 0.45 0.35
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.28 0.25 0.24 0.05
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