References
- Proceedings I(A), Weed and Environmental Impact; The 17th Asian-Pacific Weed Sciemce Society Conference Matsumoto, H.
- Proceedings, The 12th Asian-Pacific Weed Science Society Conference Ito, S.;Kamochi, A.;Sawada, K.lGoto, T.;Yasui, K.
- PCT/KR 99/00116 Kim, B. T.;Park, N. K.lHeng, K. S.;Park, J. E.;Kwon, Y. W,
- KR Pat. v.98 Kim, B. T.;Park, N. K.lHeng, K. S.;Park, J. E.
- KR Pat. v.98 Kim, B. T.;Park, N. K.lHeng, K. S.;Kwon, Y. W.
- J. Am. Chem. Soc. v.86 Hansch. C.;Fukita, T.
- Elsevier: Amsterdam QSAR and Drug Design: New Developments and Applications Fukita, T.
- J. Med. Chem. v.20 Lee, D. L.;Killman, P. A.;Marsh, F. J.;Wolff, M. E.
- ESCOM:Leiden Hugo Kubiyi 3D QSAR in Drug Design: Theory, Methods and Applications
- J. Chem. Intell, Lab. Sys. v.45 Zhou, Y. X.;Xu, L.;Wu, Y. P.;Liu, B. I.
- J. Chem., Inf. Comput. Sci. v.39 Hou, T. J;Wang, J. M.;Liao, N.;Xu, X. J.
- Angrew. Chem., Int. Ed. Engl. v.32 Gasteiger, J.;Zupan, J.
- Bioorg. med. Chem. Lett. v.2 David, J.;David, W. S.
- v.6 J. Chemomertrics Leardi, R.;Boggia, R.;Terrile, M.
- J. Chem., Inf. Comput. Sci. v.24 David, R.;Hofinger, A. J.
- J. Am. Chem. Soc. v.97 Randic, M.
- J. Med. Chem. v.41 Clare, B. W.
- J. Anal. Chem. v.18 Baumann, R. M.
- J. Mol. Biol. v.171 Sweet, R. M.;Eisenberg, D.
- Inc. Gaussian 94, Revision D.2 Frisch, M. J.;Trucks, G. W.;Schlegel, H. B.;Gill, P. M. W.;Johnson, B. G.;Robb, M. A.;Cheeseman, J. R.;Keith, T.;Petersson, G. A.;Montgomery, J. A.;Reghavachark, K.;Al-Laham, M. A.;Zakrzewski, V. G.;Ortiz, J. V.;Foresman, J. B.;Gioslowski, J.;Stefanov, B. B>;Nanauakkara, A.;Challacombe, M.;Peng, C. Y.;Ayala, P. Y.;Chen, W.;Wong, M. W.;Andres, J. L.;Repiogle, E. S.;Gomperts, R.;Martin, R. L..;Fox, D. J.;Binkley, J. S.;Defrees, D. J.;Baker, J.;Stewart, J. P.;Head-Gordon, M.;Gonzalez, C.;Pople, J. A.;Gaussian
- J. Comput. Chem. v.17 Halgren, T. A.
- J. Comput. Chem. v.17 Gundertofte, K.;Lijefors, Y.;Norrby, P. O.;Pettersson, I.
- J. Chem. Inf. Comput. Sci. v.23 Grandell, C. W.;Smith, D. H.
- J. Mol. Graphics v.5 Brint, A. T.;Willett, P.
- Melecular Simulations Inc. Gerius2 QSAR+(version 3.8)
- J. Med. Chem. v.22 Topliss, J. G.;Edwards, R. P.
Cited by
- Racemic Descriptors for Quantitative Structure Activity Relationship of Spirosuccinimide Type Aldose Reductase Inhibitors vol.25, pp.12, 2004, https://doi.org/10.5012/bkcs.2004.25.12.1874
- Optimization of Neural Networks Architecture for Impact Sensitivity of Energetic Molecules vol.26, pp.3, 2005, https://doi.org/10.5012/bkcs.2005.26.3.399
- A QSAR study of substituted benzo[a]phenazines as potential anticancer agents vol.756, pp.1, 2001, https://doi.org/10.1016/j.theochem.2005.09.010
- QSAR AND MOLECULAR DESIGN OF BENZO[B]ACRONYCINE DERIVATIVES AS ANTITUMOR AGENTS vol.6, pp.2, 2001, https://doi.org/10.1142/s0219633607003039
- Prediction of Solubility of Nonionic Solutes in Anionic Micelle (SDS) Using a QSPR Model vol.27, pp.3, 2001, https://doi.org/10.1002/qsar.200730022
- QSAR study of substituted 2-pyridinyl guanidines as selective urokinase-type plasminogen activator (uPA) inhibitors vol.24, pp.1, 2001, https://doi.org/10.1080/14756360701810355
- DFT-based QSAR and QSPR models of several cis-platinum complexes: solvent effect vol.23, pp.6, 2001, https://doi.org/10.1007/s10822-009-9265-4
- Insights through AM1 calculations into the structural requirement of N-hydroxythiosemicarbazone analogs as anti-tubercular agents vol.24, pp.3, 2001, https://doi.org/10.1080/14756360802421094
- Exploration of QSAR modelling techniques and their combination to rationalize the physicochemical characters of nitrophenyl derivatives towards aldose reductase inhibition vol.24, pp.4, 2001, https://doi.org/10.1080/14756360802565486
- Identification of KT-15073 as an Inhibitor of Lipopolysaccharide-Induced Microglial Activation vol.33, pp.3, 2001, https://doi.org/10.1248/bpb.33.461
- Quantitative structure-activity relationship study of nonpeptide antagonists of CXCR2 using stepwise multiple linear regression analysis vol.141, pp.1, 2010, https://doi.org/10.1007/s00706-009-0225-4
- Receptor-based QSAR study for a series of 3,3-disubstituted-5-aryl oxindoles and 6-aryl benzimidazol-2-ones derivatives as progesterone receptor inhibitors vol.22, pp.7, 2001, https://doi.org/10.1080/1062936x.2011.623324
- Topological, hydrophobicity, and other descriptors on α-glucosidase inhibition: a QSAR study on xanthone derivatives vol.26, pp.6, 2011, https://doi.org/10.3109/14756366.2010.549089
- 4D-QSAR Study of p56Ick Protein Tyrosine Kinase Inhibitory Activity of Flavonoid Derivatives Using MCET Method vol.32, pp.12, 2001, https://doi.org/10.5012/bkcs.2011.32.12.4352
- Prediction of the relationship between the structural features of andrographolide derivatives and α慣-glucosidase inhibitory activity: A quantitative structure-activity relationship (QSAR) Study vol.26, pp.1, 2001, https://doi.org/10.3109/14756361003724760
- A quantitative structure-property relationships study of the stability constant of crown ethers by molecular modelling: new descriptors for lariat effect vol.70, pp.1, 2001, https://doi.org/10.1007/s10847-010-9854-9
- QSAR study of a series of cholesteryl ester transfer protein inhibitors vol.76, pp.7, 2001, https://doi.org/10.1135/cccc2011019
- Simple QSPR Modeling for Prediction of the GC Retention Indices of Essential Oil Compounds vol.18, pp.6, 2001, https://doi.org/10.1080/0972060x.2014.884768