참고문헌
- Akamatsu, M. (2002) Current state and perspectives of 3D-QSAR. Curr. Topics Med. Chem. 2:1381 - 1394 https://doi.org/10.2174/1568026023392887
- Albores-Velasco, M., J. John and R. L. Wain (1995) Fungicidal activity of phenyl N-( 4-substituted-phenyl) thionocarbamates. J. Agric. Food Chem. 43:2260 - 2261 https://doi.org/10.1021/jf00056a054
- Clark, M., R. D. Cramer III, D. M. Jones, D. E. Patterson and P. E. Simeroth (1990) Comparative molecular field analysis (CoMFA). 2. Toward its use with 3D-structural databases, Tetrahedron Comput. Methodol. 3:47-59 https://doi.org/10.1016/0898-5529(90)90120-W
- Copping, L. G., and H. G. Hewitt (1998) Chemistry and Mode of Action of Crop Protection Agents. pp. 93, The Royal Society of Chemistry. lnformation Services. Cambridge, UK
- Cramer, R. D., D. E. Patterson and J. D. Bunce (1988) Comparative molecular field analysis (CoMFA), 1. Effect of shape on the binding of steroids to carrier proteins, J. Am. Chem. Soc. 110:5959 - 5967 https://doi.org/10.1021/ja00226a005
- Cramer, R. D., J. D. Bunce and D. E. Patterson (1988) Cross-validation, Bootstrapping and partial least squares compared with multiple regression in conventional QSAR studies. Quant. Struct. Act. Relat. 7:18-25 https://doi.org/10.1002/qsar.19880070105
- Kamoshita, K., C. Takayama, J. Takahashi and A. Fujinami (1992) Application of the Hansch-Fujita method to the design of imide and carbamate fungicides. pp.430 - 443, In Rational Approaches to Structure, Activity, and Ecotoxicology of Agrochemicals. (ed. Draber, W. and Fujita, T.) CRC Press Inc., London
- Kellogg, G. E., S. F. Semus and D. J. Abraham (1991) HINT: A new method of empirical hydophobic field calculation for CoMFA. J. Comput.-Aided Mol. Des. 5:545-552 https://doi.org/10.1007/BF00135313
- Kerr, R. (1994) Parallel helix bundles and ion channels: molecular modeling via simulated annealing and restrained molecular dynamics. Biophys. J. 67:1501-1515 https://doi.org/10.1016/S0006-3495(94)80624-1
- Klebe, G. (1993) Structural Alignment of Molecules. pp.173-199, In 3D-QSAR Drug Design, Theory, Methods and Applications (ed. Kubinyi, H.), ESCOM. Leiden
- Maksic, I. B. (1987) Modeling of Structure and Properties of Molecules, Ellis Horwood Ltd
- Marshall, G. R., C. D. Barry, H. E. Bosshard, R. A. Dammkoehler and D. A. Dunn (1979) The conformational parameter in drug design; active analog approach. pp.205 -226. In Computer-assisted drug design (ed. Olsen, E. C. and Christoffersen, R. E.), ACS, Washington, D.C
- Purcell, W. P. and J. A. Singer (1967) A brief review and table of serniempirical parameters used in the Huckel molecular orbital method. J. Chem. Eng. Data. 122:235-246
- Robert, D. C. and C. F. Peter (2004) Statistical variation in progressive scrambling. J. Comp.-Aided Mol. Des. 18:563-576 https://doi.org/10.1007/s10822-004-4077-z
- Staub, T. (1991) Fungicide resistance practical experience with anti-resistance strategies and the role of integrated use, Ann. Rev. Phytopathol. 29:421-442 https://doi.org/10.1146/annurev.py.29.090191.002225
- Sung, N. D. and M. G. Seong (1999) Phenyl substituent effect on the fungicidal activity of N-phenylthionocarbamate derivatives. Kor. J. Pestic. Sci. 3:29-36
- Tomoya Y., S. Kayo, S. Koichi, U. Shinji, Y. Setsuko, S. Tokuo, K. Satoshi., O. Yasuyoshi and S. Takaki (2005) Functional genomics may allow accurate categorization of the benzimidazole fungicide benomyl: Lack of ability to act via steroid-receptor-mediated mechanisms., Toxicol. and Appl. Pharmacol. 205:11-30 https://doi.org/10.1016/j.taap.2004.09.002
- Tripos Associates, Inc., 1699 S. Hanley Road, Suite 303, St. Louis, MO. 63144-2913, U.S.A
- You, J. W. (2005) 3D-QSAR models and their predictability on the fungicidal activity of N-phenyl thionocarbamate derivatives. M.Sc. Degree Thesis. Graduate School, Chungnam National University, Daejeon, Korea