Song, Jong-Hwan
(Cytosine Laboratory, Korea Research Institute of Chemical Technology)
Park, Kyung-Yong (Division of Applied Biologies and Chemistry, College of Agriculture and Life Science, Chungnam National University) Sung, Nack-Do (Division of Applied Biologies and Chemistry, College of Agriculture and Life Science, Chungnam National University) |
1 | Bauer, N., Fajans, K. and Lewin, S. Z. (1960) Technique of Organic Chemistry, Vol. 1., Part ll, Wissberger, A. (ed.), Interscience, New York, p. 1139 |
2 | Tripos Associates, Inc., 1699 S. Hanley Road, Suite 303, St. Louis, MO 63144-2913, U.S.A., /.http://www.tripos.com/Bookshelf/qsar |
3 | Sung, N, D., (1989) Solvent dependence and component of linear free energy relationship on the chemical shift of methylene proton in 1-(Phenoxymethyl)benzotriazole derivatives. J. Kor. Chem. Soc. 33(5), 538-544 |
4 | Theodoridis, G., Bahr, J. T., Hotzman, F. W., Sehgel, S. and Suarez, D. P. (2000) New geration of protox-inhibiting herbicides, Crop Prot. 19, 533-535 DOI ScienceOn |
5 | Sung, N. D., Song, J. H. and Park, K. Y. (2004) Understanding the herbicidal activity of novel 1-(5-methyl-3-phenylisoxazolin-5-yl)methioxy-2-chloro-4-fluorobenzene derivatives as protox inhibitors using holographic quantitatives structure-activity relationship (HQSAR) methodology, J. Kor. Soc. Appl. Biol. Chem. 47(3), 351- 356 |
6 | Sung, N. D., Song, J. H., Yang, S. Y. and Park, K. Y. (2004) Understanding the herbicidal activity of novel 1-(5-methyl-3-phenylisoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivatives as protox inhibitors using comparatives molecular field analyses (CoMFA) methodology, Kor. J. Pest. Sci. 8(3), 151-161 |
7 | Sung, N. D., Ock, H. S., Chung, H. J. and Song, J. H. (2003) Quantitative structu- re-activity relationships and molecular shape similarity of the herbicidal N-substituted phenyl-3,4-dimethylmaleimide derivatives, Kor. J. Pest. Sci. 7(2), 100-107 |
8 | Waller, C. L. and Marshall, G. R. (1993) Three-dimensional quantitative structure- activity relationship of angiotesin converting enzyme and thermolysin inhibitors. 11. Acomparasion of CoMFA models incorporating molecular orbital fields and desolvation free energies based on active-analog and complementary-receptor-field alignment rules. J. Med. Chem. 36, 2390-2403 DOI ScienceOn |
9 | Cramer, R. D. lll., Bunce, J. D. and Patterson, D. E. (1988) Crossvalidation, bootstrapping, and partial least squares compared with multiple regression in conventional JAR studies. Quant. Struct. Act. Relat. 7, 18-25 DOI |
10 | Pallett, K. E. (1997) Herbicide target sites, recent trends and new challenges, Proceeding of Brighton Crop Protection Conference-Weeds, pp. 575-578 |
11 | Stahle, L. and Wold, S. (1988) Multivariate data analysis and experimental design in biomedical research. Progr. Med. Chem. 25, 292-334 |
12 | Stewart, J. J. (1990) MOPAC: A semiempirical molecular orbital program. J. Comp.-Aided Mol. Design. 4, 1-105 DOI |
13 | Kim, K. H. (1993) hi 3D QSAR Drug Design, Theory, Methos and Applications: Comparison of classical and 3D-QSAR. Kubinyi, H. (ed.), ESCOM. Leiden, pp. 619-642 |
14 | Boger, P and Wakabayashi, K. (1999) Peroxidizing Herbicides, Springer-Verlag Berline Heidelberg. Germany |
15 | Wold, S., Albano, C., Dunn, W. J., Edlund, U., Esbensen, K., Gelaae?, P., Hellberg, S., Johanasson, F., Lindberg, W. and Sjostrom, M. (1984) In Chemometrics: Mathematics and Statistics in Chemistry Multivariate Data Analysis in Chemistry, Kowalski, B. R. (ed.), Reidel, Dordrecht, Nethelands. pp. 12-94 |
16 | Kubinyi, H. (1993) 3D QSAR Drug Design, Theory, Methos and Applications, ESCOM. Leiden |
17 | Klebe, G. and Abraham, U. (1999) Comparative molecular similarity indices analyisis (CoMSIA) to study hydrogenbonding properties and to score combinatorial libraries. J. Comput. Aid. Mol. Des. 13, 1-10 DOI ScienceOn |
18 | Sung, N. D., Ock, H. S., Chung, H. J,. Song, J. H. and Lee, Y. G. (2003) Comparatives molecular field analyses (CoMFA) on the growth inhibition activity of N-phenyl-3,4,5,6-tetrahydrophthalimide and N-phenyl-3,4-dimethylmaleimide derivatives. Kor. J. Pest. Sci. 7(2), 75-82 |
19 | Lien, E. J., Guo, Z. R., Li, R. L. and Su, C. T. (1982) Use of dipole moment as parameter in drug receptor; Interaction and quantitative structure activity relationship studies. J. Pharm. 71, 641-655 DOI |
20 | Ryu, E. K., Jeon, D. J., Song, J. H. and Kim, H. R. (2001) Herbicidal 2-(5-isoxa-zolmylmethyloxyphenyl)-4,5,6,7-tetrahydro-2H-indazo1e derivatives. Korean Pat. 0289470 |
21 | QCPE; Quantum Chemistry Program Exchange, Creative Arts Building 181, Indiana Univ., Bloomington, Indiana 47405, U.S.A |
22 | Dewar, M. J. S., Zoebish, E. G., Healy, E. F. and Stewart, J. J. P. (1985) AMl: A new general purpose quantum mechanical molecular model. J. Am. Chem. Soc. 107, 3902-3909 DOI |
23 | Marshall, G. R., Barry, C. D., Bosshard, H. E., Dammkoehler, R. A. and Dunn, D. A. (1979) In Computer-assisted drug design: The conformational parameter in drug design; active analog approach. Olsen, E. C. and Christoffersen, R. E. (eds.), Ammerican Chemical Society, Washington, D.C., pp. 205-226 |
24 | Fujita, T. (2002) In Agrochemical Discovery, Insect, Weed, and Fungal control: Similarities in bioanalogous structural transformation patterns, Ch. 15, Baker, D. R. and Umetsu, N. K. (eds.), ACS Symposium Series No. 774, American Chemical Society, Washington, DC |
25 | Uraguchi, R., Sato, Y., Nakayama, A., Sukekawa, M., Iwataki, I., Boger, P. and Wakabayashi, K. (1997) Molecular shape similarity of cyclic imides and protoporphyrinogen IX. J. Pestic. Sci. 22, 314-320 |
26 | Kerr, R. et al., (1994) Parallel helix bundles and ion channels: molecular modeling via simulated annealing and restrained molecular dynamics. Biophys. J. 67, 1501-1515 DOI ScienceOn |