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    새로운 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one 유도체들의 제초활성에 관한비교 분자장 분석 모델과 선택성 = Comparative Molecular Field Analyses (CoMFA) Models and Their Selectivity for the Herbicidal Activities of New Novel 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7- ..

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    https://www.riss.kr/link?id=A104738560

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    The comparative molecular field analyses (CoMFA) models for the herbicidal activities against barnyardgrass (Echinochloa crus-galli) and rice plant (Orysa sativa L.) by the substituent (R) on the hexahydroisoindol-1-one ring in a series of new 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one derivatives were conducted and discussed for selectivity between both plants. The statistical results of the two best models (B2 & R7) showed the best predictability for the herbicidal activities based on the cross-validated value q2 (r2cv. = 0.529~ 0.755)and none cross-validated value (r2 ncv.= 0.937~0.945), respectively. Based on the findings, the predictability and fitness of the model (B2) for barnyard grass was better than that of the model (R7) for rice plant. From the two models and contour maps, it is revealed that the novel selective character for herbicidal activity between the two plants depend on the electrostatic field and steric field for the substituent of ortho-positions on the S-phenyl group as R-substituent in hexahydroisoindol-1-one ring.
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    The comparative molecular field analyses (CoMFA) models for the herbicidal activities against barnyardgrass (Echinochloa crus-galli) and rice plant (Orysa sativa L.) by the substituent (R) on the hexahydroisoindol-1-one ring in a series of new 2-(4-ch...

    The comparative molecular field analyses (CoMFA) models for the herbicidal activities against barnyardgrass (Echinochloa crus-galli) and rice plant (Orysa sativa L.) by the substituent (R) on the hexahydroisoindol-1-one ring in a series of new 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one derivatives were conducted and discussed for selectivity between both plants. The statistical results of the two best models (B2 & R7) showed the best predictability for the herbicidal activities based on the cross-validated value q2 (r2cv. = 0.529~ 0.755)and none cross-validated value (r2 ncv.= 0.937~0.945), respectively. Based on the findings, the predictability and fitness of the model (B2) for barnyard grass was better than that of the model (R7) for rice plant. From the two models and contour maps, it is revealed that the novel selective character for herbicidal activity between the two plants depend on the electrostatic field and steric field for the substituent of ortho-positions on the S-phenyl group as R-substituent in hexahydroisoindol-1-one ring.

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    국문 초록 (Abstract) kakao i 다국어 번역

    새로운 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one 유도체의 hexahydroisoindol-1-one 고리상 R-치환기 변화에 따른 논피(Echinochloa crusgalli)와 벼(Orysa sativa L.)에 대한 제초활성에 관한 비교 분자장 분석(CoMFA) 모델을 유도하고 두 초종에 대한 선택성에 관하여 논의하였다. 가장 양호한 두 모델(B2 및 R7)의 통계결과는 교차 확인값 q2(r2cv.= 0.529~0.755)과 비교차 확인값(r2ncv.=0.937~0.945)에 기초하여 가장 양호한 예측성을 보였다. 그리고 논피에 대한 모델(B2)의 예측성과 적합성이 벼에 대한 모델(R7) 보다도 통계적으로 양호하였다. 또한, 두 모델과 기여도로부터 정전기장과 hexahydroisoindol-1-one 고리상 S-phenyl 기의 ortho-위치에 있는 입체장이 두 초종 간 선택적인 제초활성에미치는 중요한 요소이었다.
    번역하기

    새로운 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one 유도체의 hexahydroisoindol-1-one 고리상 R-치환기 변화에 따른 논피(Echinochloa crusgalli)와 벼(Orysa sativa L.)에 대한 제...

    새로운 2-(4-chloro-5-(2-chloroallyloxy)-2-fluorophenyl)-3-thioalkoxy-2,3,4,5,6,7-hexahydroisoindol-1-one 유도체의 hexahydroisoindol-1-one 고리상 R-치환기 변화에 따른 논피(Echinochloa crusgalli)와 벼(Orysa sativa L.)에 대한 제초활성에 관한 비교 분자장 분석(CoMFA) 모델을 유도하고 두 초종에 대한 선택성에 관하여 논의하였다. 가장 양호한 두 모델(B2 및 R7)의 통계결과는 교차 확인값 q2(r2cv.= 0.529~0.755)과 비교차 확인값(r2ncv.=0.937~0.945)에 기초하여 가장 양호한 예측성을 보였다. 그리고 논피에 대한 모델(B2)의 예측성과 적합성이 벼에 대한 모델(R7) 보다도 통계적으로 양호하였다. 또한, 두 모델과 기여도로부터 정전기장과 hexahydroisoindol-1-one 고리상 S-phenyl 기의 ortho-위치에 있는 입체장이 두 초종 간 선택적인 제초활성에미치는 중요한 요소이었다.

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    참고문헌 (Reference)

    1 "and partial least squares comparedwith multiple regression in conventional QSAR studies" 198818-25

    2 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-structure-activity relationship (HQSAR) methodology" 47 : 351-356, 2004

    3 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenyl-isoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular similarity indices analysis (CoMSIA)methodology" 47 : 414-421, 2004

    4 "Understanding the protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular field analysis (CoMFA)methodology" 8 : 151-161, 2004

    5 "Toward its use with 3D-structuraldatabases" 47-59, 1990

    6 "Three dimensional quantitative structure-activity relationshipanalyses on the fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives usingthe comparative molecular similarity indices analyses(CoMSIA) methodology based on the different alignmentapproaches" 9 : 26-34, 2005

    7 "Three dimensional quantitative structure-activity relationship onthe fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives using the compar- ativemolecular field analyses methodology based on thedifferent alignment approaches" 48 : 82-88, 2005

    8 "The conformational parameter in drug design" In Computer-assisted drugdesign 205-226, 1979

    9 "Quantitative structure-activity relationships and molecular shapesimilarity of the herbicidal N-substituted phenyl-3, 4-dimethylmaleimideDerivatives" 7 : 100-107, 2003

    10 "New geration of protox-inhibitingherbicides" 19 : 533-535, 2000

    1 "and partial least squares comparedwith multiple regression in conventional QSAR studies" 198818-25

    2 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-structure-activity relationship (HQSAR) methodology" 47 : 351-356, 2004

    3 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenyl-isoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular similarity indices analysis (CoMSIA)methodology" 47 : 414-421, 2004

    4 "Understanding the protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular field analysis (CoMFA)methodology" 8 : 151-161, 2004

    5 "Toward its use with 3D-structuraldatabases" 47-59, 1990

    6 "Three dimensional quantitative structure-activity relationshipanalyses on the fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives usingthe comparative molecular similarity indices analyses(CoMSIA) methodology based on the different alignmentapproaches" 9 : 26-34, 2005

    7 "Three dimensional quantitative structure-activity relationship onthe fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives using the compar- ativemolecular field analyses methodology based on thedifferent alignment approaches" 48 : 82-88, 2005

    8 "The conformational parameter in drug design" In Computer-assisted drugdesign 205-226, 1979

    9 "Quantitative structure-activity relationships and molecular shapesimilarity of the herbicidal N-substituted phenyl-3, 4-dimethylmaleimideDerivatives" 7 : 100-107, 2003

    10 "New geration of protox-inhibitingherbicides" 19 : 533-535, 2000

    11 "Molecular shapesimilarity of cyclic imides and protoporphyrinogen IX" 22 : 314-320, 1997

    12 "In Rational Approaches to Structure andEcotoxicology of Agrochemicals Application of the Hansch-Fujita Method to the Design of Imide and carbamatefungicides" CRCPress chap : 1992

    13 "In PeroxidizingHerbicides" Springer-Verlag Berline Heidelberg 1999

    14 "In Chemistry andMode of Action of Crop Protection Agents" 1998

    15 "In Agrochemical Discovery, Insect, Weed, andFungal control: Similarities in bioanalogous structuraltransformation patterns" AmericanChemical Society (774) : 2002

    16 "Effect ofshape on the binding of steroids to carrier proteins" 5959-5967, 1988

    17 "Effect of 3-thioalkoxy groups on herbicidalactivities of 2-(5-alkoxyphenyl)-3-phenylthioisoindoline-1-oneDerivatives" Chung-nam National University 5-, 2002

    18 "Comparative molecular field analyses (CoMFA) on the growthinhibition activity of N-phenyl-3,4,5,6-tetra-hydrophtalimide andN-phenyl-3,4-dimethylmaleimide Derivatives" 7 : 75-82, 2003

    19 "A brief review and tableof semiempirical parameters used in the Huckel molecularorbital method" 235-246, 1967

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    학술지 이력
    연월일 이력구분 이력상세 등재구분
    2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
    2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
    2015-12-30 학술지명변경 한글명 : Journal of the Korean Society for Applied Biological Chemistry -> Applied Biological Chemistry
    외국어명 : Journal of the Korean Society for Applied Biological Chemistry -> Applied Biological Chemistry
    KCI등재
    2010-05-06 학술지명변경 한글명 : 한국응용생명화학회지 -> Journal of the Korean Society for Applied Biological Chemistry KCI등재
    2010-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2008-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2006-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2004-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2001-07-01 등재 등재학술지 선정 (등재후보2차) KCI등재
    1999-01-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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    기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
    2016 0.81 0.21 0.61
    KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
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