RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재후보

      Hologram Based QSAR Analysis of Caspase-3 Inhibitors

      한글로보기

      https://www.riss.kr/link?id=A105453645

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Caspases, a family of cysteinyl aspartate-specific proteases plays a central role in the regulation and the execution of apoptotic cell death. Caspase-3 has been proven to be an effective target for reducing the amount of cellular and tissue damage because the activation of caspases-3 stimulates a signalling pathway that ultimately leads to the death of the cell. In this study, Hologram based Quantitative Structure Activity Relationship (HQSAR) models was generated on a series of Caspase-3 inhibitors named 3, 4-dihydropyrimidoindolones derivatives. The best HQSAR model was obtained using atoms, bonds, and hydrogen atoms (A/B/H) as fragment distinction parameter using hologram length 61 and 3 components with fragment size of minimum 5 and maximum 8. Significant cross-validated correlation coefficient ($q^2=0.684$) and non cross-validated correlation coefficients ($r^2=0.754$) were obtained. The model was then used to evaluate the eight external test compounds and its $r^2_{pred}$ was found to be 0.559. Contribution map show that presence of pyrrolidine sulfonamide ring and its bulkier substituent's makes big contributions for improving the biological activities of the compounds.
      번역하기

      Caspases, a family of cysteinyl aspartate-specific proteases plays a central role in the regulation and the execution of apoptotic cell death. Caspase-3 has been proven to be an effective target for reducing the amount of cellular and tissue damage be...

      Caspases, a family of cysteinyl aspartate-specific proteases plays a central role in the regulation and the execution of apoptotic cell death. Caspase-3 has been proven to be an effective target for reducing the amount of cellular and tissue damage because the activation of caspases-3 stimulates a signalling pathway that ultimately leads to the death of the cell. In this study, Hologram based Quantitative Structure Activity Relationship (HQSAR) models was generated on a series of Caspase-3 inhibitors named 3, 4-dihydropyrimidoindolones derivatives. The best HQSAR model was obtained using atoms, bonds, and hydrogen atoms (A/B/H) as fragment distinction parameter using hologram length 61 and 3 components with fragment size of minimum 5 and maximum 8. Significant cross-validated correlation coefficient ($q^2=0.684$) and non cross-validated correlation coefficients ($r^2=0.754$) were obtained. The model was then used to evaluate the eight external test compounds and its $r^2_{pred}$ was found to be 0.559. Contribution map show that presence of pyrrolidine sulfonamide ring and its bulkier substituent's makes big contributions for improving the biological activities of the compounds.

      더보기

      참고문헌 (Reference)

      1 D. K. Perry, "Zinc is a potent inhibitor of the apoptotic protease, caspase-3. a novel target for zinc in the inhibition of apoptosis" 272 : 18530-18533, 1997

      2 B. H. Han, "Selective, reversible caspase-3 inhibitor is neuroprotective and reveals distinct pathways of cell death after neonatal hypoxic-ischemic brain injury" 277 : 30128-30136, 2002

      3 J. Wang, "Roles of caspases in apoptosis, development and cytokine maturation revealed by homozygous gene deficiencies" 113 : 753-757, 2000

      4 M. Thirumurthy, "QSAR analysis on PfPK7 inhibitors using HQSAR, CoMFA and CoMSIA" 21 : 681-693, 2012

      5 D. V. Kravchenko, "Pyrrolo[3,4-c]quinoline-1,3-diones as potent caspase-3 inhibitors. Synthesis and SAR of 2-sub- stituted 4-methyl-8-(morpholine-4-sulfonyl)-pyrrolo [3,4-c]quinoline-1,3-diones" 40 : 1377-1383, 2005

      6 M. D. Jacobson, "Pro-grammed cell death in animal development" 88 : 347-354, 1997

      7 D. Lee, "Potent and selective non pep- tide inhibitors of caspase 3 and 7" 44 : 2015-2026, 2001

      8 C. W. Scott, "Novel small molecule inhibitors of caspase-3 block cellular and bio-chemical features of apoptosis" 304 : 433-440, 2003

      9 W. Chu, "N-Benzylisatin sulfonamide analogues as potent caspase-3 inhibitors: Synthesis, in vitro activity and molecular modeling studies" 48 : 7637-7647, 2005

      10 T. W Heritage, "Molecular Holo-gram QSAR;Rational Drug Design" American Chemical Society 719 : 212-225, 2000

      1 D. K. Perry, "Zinc is a potent inhibitor of the apoptotic protease, caspase-3. a novel target for zinc in the inhibition of apoptosis" 272 : 18530-18533, 1997

      2 B. H. Han, "Selective, reversible caspase-3 inhibitor is neuroprotective and reveals distinct pathways of cell death after neonatal hypoxic-ischemic brain injury" 277 : 30128-30136, 2002

      3 J. Wang, "Roles of caspases in apoptosis, development and cytokine maturation revealed by homozygous gene deficiencies" 113 : 753-757, 2000

      4 M. Thirumurthy, "QSAR analysis on PfPK7 inhibitors using HQSAR, CoMFA and CoMSIA" 21 : 681-693, 2012

      5 D. V. Kravchenko, "Pyrrolo[3,4-c]quinoline-1,3-diones as potent caspase-3 inhibitors. Synthesis and SAR of 2-sub- stituted 4-methyl-8-(morpholine-4-sulfonyl)-pyrrolo [3,4-c]quinoline-1,3-diones" 40 : 1377-1383, 2005

      6 M. D. Jacobson, "Pro-grammed cell death in animal development" 88 : 347-354, 1997

      7 D. Lee, "Potent and selective non pep- tide inhibitors of caspase 3 and 7" 44 : 2015-2026, 2001

      8 C. W. Scott, "Novel small molecule inhibitors of caspase-3 block cellular and bio-chemical features of apoptosis" 304 : 433-440, 2003

      9 W. Chu, "N-Benzylisatin sulfonamide analogues as potent caspase-3 inhibitors: Synthesis, in vitro activity and molecular modeling studies" 48 : 7637-7647, 2005

      10 T. W Heritage, "Molecular Holo-gram QSAR;Rational Drug Design" American Chemical Society 719 : 212-225, 2000

      11 K. M. Boatright, "Mechanisms of caspase activation" 15 : 725-731, 2003

      12 J. Schoenberger, "Innovative strategies in in-vivo apoptosis imaging" 15 : 187-194, 2008

      13 Sathya. B, "Homology Modelling of Chemerin like Receptor-1 (CMKLR1): Potential Target for Treating Type II Diabetes" 기초과학연구원 10 (10): 20-26, 2017

      14 D. A Winkler, "Holographic QSAR of benzodiazepines" 17 : 224-231, 1998

      15 Sathya Babu, "Hologram Based QSAR Analysis of Xanthine Oxidase Inhibitors" 기초과학연구원 10 (10): 202-208, 2017

      16 Tripos Sybyl, "HQSAR manual"

      17 W. Tong, "Evaluation of quantitative structure-activity relationship methods for large-scale prediction of chemicals binding to the estrogen receptor" 38 : 669-677, 1998

      18 A. G. Porter, "Emerging roles of caspase 3 in apoptosis" 6 : 99-104, 1999

      19 Sathya Babu, "Docking Study of Corticotropin-Releasing Factor-1 Receptor with Its Antagonists" 기초과학연구원 11 (11): 19-24, 2018

      20 S. Wold, "Cross-validatory estimation of the num- ber of components in factor and principal component model" 20 : 397-405, 1978

      21 G. M. Cohen, "Caspases: the executioners of apoptosis" 326 : 1-16, 1997

      22 C. B. Thonberry, "Caspases: enemied within" 281 : 1312-1316, 1998

      23 D. W. Nicolson, "Caspase structure, proteolytic substrates, and function during apoptotic cell death" 6 : 1028-1042, 1999

      24 B. A. Callus, "Caspase inhibitors: viral, cellular and chemical" 14 : 73-78, 2007

      25 R. S. Hotchkiss, "Caspase inhibitors improves survival in sepsis: a critical role of the lymphocyte" 1 : 496-501, 2000

      26 H. Yaoita, "Attenuation of ischemia/reperfusion injury in rats by a caspase inhibitor" 97 : 276-281, 1998

      27 M. Endres, "Attenuation of delayed neuronal death after mild focal ischemia in mice by inhibition of caspase family" 18 : 238-247, 1998

      28 C. L. Waller, "A comparative QSAR study using CoMFA, HQSAR, and FRED/SKEYS paradigms for estrogen receptor binding affinities of structur- ally diverse compounds" 44 : 758-765, 2004

      29 L. M. Havran, "3.4-Dihydropyrimido (1,2-a indol-10(2H)-ones as potent non-peptidic inhibitors of caspase-3" 17 : 7755-7768, 2009

      더보기

      동일학술지(권/호) 다른 논문

      동일학술지 더보기

      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      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
      더보기

      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
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼