최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기농약과학회지 = The Korean journal of pesticide science, v.15 no.1, 2011년, pp.68 - 85
초록이 없습니다.
성낙도 (2003) 정량적인 구조-활성상관(QSAR) 기법에 의한 새로운 농약의 개발 - IV. 국내의 연구 동향과 전망, Journal of the Korean Society for Applied Biological Chemistry, 46(3), pp. 155-164.
성낙도, 송선섭 (2003a), 제초제의 활성성분에 대한 물리화학 파라미터의 범위, 학국농약과학회지 7(1), 58-65.
성낙도, 송선섭 (2003b) 작물보호제로서 살군제와 살충제의 활성성분에 대한 물리-화학 파라미터의 범위, J. Korean Soc. for Agric. Chem. Biotechnol. 46(4), 280-284.
Akinori Hirashim, Eiichi Kuwano, Morifusa Eto (2003), Com-parative receptor surface analysis of octopaminergic antagonists for the locust neuronal octopamine receptor, Computational Biology and Chemistry 27:531-540.
Andrade, C.; Salum, L.B.; Castilho, M.; Pasqualoto, K.; Ferreira, E.; Andricopulo, A. (2008), Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Mol. Divers. 12, 47-59.
Casalegno M.; Sello G. Benfenati E. (2006), Top-Priority Frag-ment QSAR Approach in Predicting Pesticide Aquatic Toxicity. Chem. Res. Toxicol. 19, 1533-1539.
Chunyan Zhao, Elena Boriani, Antonio Chana, Alessandra Roncaglioni, Emilio Benfenati (2008), A new hybrid system of QSAR models for predicting bioconcentration factors (BCF), Chemosphere 73:1701-1707.
Cramer, R.; Patterson, D.; Bunce, J. 1988, Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins. J. Am. Chem. Soc. 110, 5959-5967.
D. J. de Ridder, L. Villacorte, A.R.D. Verliefde, J.Q.J.C. Verberk, S.G.J. Heijman, G.L. Amy, J.C. van Dijk (2010), Modeling equilibrium adsorption of organic micropollutants onto activated carbon, water research 44:3077-3086
Frank E. Blaney, Dorica Naylor, and John Woods (1993), MAMBAs: A real-time graphics environment for QSAR, J. Mol. Graphics 11: September 157-165.
Hopfinger, A.J.; Wang, S.; Tokarski, J.S.; Jin, B.; Albuquerque, M.; Madhav, P.J.; Duraiswami, C. (1997), Construction of 3D-QSAR models using the 4D-QSAR analysis formalism. J. Am. Chem. Soc. 119, 10509-10524.
Joop Hermens (1995), Prediction of environmental toxicity based on structure-activity relationships using mechanistic information, The Science of the Total Environment 171: 235-242.
Klebe, G.; Abraham, U., Mietzner, T. (1994), Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity. J. Med. Chem. 37, 4130-4146.
Kyaw Zeyar Myint, Xiang-Qun Xie, (2010) Recent Advances in Fragment-Based QSAR and Multi-Dimensional QSAR Methods, Int. J. Mol. Sci., 11: 3846-3866.
Linnan He, Peter C. Jurs (2005), Assessing the reliability of a QSAR model's predictions, Journal of Molecular Graphics and Modelling 23:503-523.
Luis G. Valerio Jr. (2009), In silico toxicology for the phar-maceutical sciences, Toxicology and Applied Pharmacology 241:356-370.
Mark T.D. Cronin, T. Wayne Schultz (2003), Pitfalls in QSAR, Journal of Molecular Structure (Theochem) 622:39-51.
Markus A. Lill (2007), Multi-dimensional QSAR in drug discovery, Drug Discovery Today 12(23/24), pp. 1013-1017.
Markus Boehm (2011), Virtual Screening of Chemical Space: From Generic Compound Collections to Tailored Screening Libraries, pp. 5.
Matthew S. Sigman, Jeremie J. Miller (2009), Examination of the Role of Taft-Type Steric Parameters in Asymmetric Catalysis, J. Org. Chem. 74:7633-7643.
Nicholas E. Jewell, David B. Turner, Peter Willett, Graham J. Sexton (2001), Automatic generation of alignments for 3D QSAR analyses, Journal of Molecular Graphics and Modelling 20:111-121.
Ourania Peristera, Morena Spreafico, Martin Smiesko, Beat Ernst, Angelo Vedani (2009), Mixed-model QSAR at the human mineralocorticoid receptor: Predicting binding mode and affinity of anabolic steroids, Toxicology Letters 189:219-24.
Ourania Peristera, Morena Spreafico, Martin Smiesko, Beat Ernst, Angelo Vedani. (2009) Mixed-model QSAR at the human mineralocorticoid receptor: Predicting binding mode and affinity of anabolic steroids, Toxicology Letters 189, 219- 224.
Pastor, M.; Cruciani, G.; McLay, I.; Pickett, S.; Clementi, S. (2000), GRid-INdependent descriptors (GRIND): A novel class of alignment-independent three-dimensional molecular descriptors. J. Med. Chem. 43, 3233-3243.
Robinson, D.D.; Winn, P.J.; Lyne, P.D.; Richards, W.G. (1999), Self-organizing molecular field analysis: A tool for structure-activity studies. J. Med. Chem. 42, 573-583.
Shane Weaver, M. Paul Gleeson (2008), The importance of the domain of applicability in QSAR modeling, Journal of Molecular Graphics and Modelling 26:1315-1326.
Shunlai Li, Yan Zheng (2006), Self-Organizing Molecular Field Analysis on a New Series of COX-2 Selective Inhibitors: 1,5-Diarylimidazoles, Int. J. Mol. Sci. 7, 220-229.
Silverman, B.D.; Platt, D.E. (1996), Comparative molecular moment analysis (CoMMA): 3D-QSAR without molecular superposition. J. Med. Chem. 39, 2129-2140.
Supratik Kar, Kunal Roy (2010), QSAR modeling of toxicity of diverse organic chemicals to Daphnia magna using 2D and 3D descriptors, Journal of Hazardous Materials 177 : 344-351
Vivek VYAS, Anurekha JAIN, Avijeet JAIN, Arun GUPTA (2008), Virtual Screening: A Fast Tool for Drug Design, Sci Pharm. 76:333-360.
Wagener, M.; Sadowski, J.; Gasteiger, J. (1995), Autocorrelation of molecular surface properties for modeling corticosteroid binding globulin and cytosolic ah receptor activity by neural networks. J. Am. Chem. Soc. 117, 7769-7775.
Yovani Marrero Ponce (2004), Total and local (atom and atom type) molecular quadratic indices: significance interpretation, comparison to other molecular descriptors, and QSPR/QSAR applications Bioorganic & Medicinal Chemistry 12:6351-6369.
Zhokhova, N.; Baskin, I.; Palyulin, V.; Zefirov, A.; Zefirov, N. (2007), Fragmental descriptors with labeled atoms and their application in QSAR/QSPR studies. Doklady Chem. 417, 282-284.
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
Free Access. 출판사/학술단체 등이 허락한 무료 공개 사이트를 통해 자유로운 이용이 가능한 논문
※ AI-Helper는 부적절한 답변을 할 수 있습니다.