By Corwin Hansch, Toshio Fujita
content material: prestige of QSAR on the finish of the 20th century / Corwin Hansch and Toshio Fujita --
Quantitative structure-activity research and database-aided bioisosteric structural transformation process as methodologies of agrochemical layout / Toshio Fujita --
Hydrophobicity parameter of heteroaromatic compounds derived from numerous partitioning structures / Chisako Yamagami and Toshio Fujita --
Theoretical estimation of octanol-water partition coefficient for organophosphorus insecticides / Toshiyuki Katagi, Masakazu Miyakado, Chiyozo Takayama, and Shizuya Tanaka --
The calculation of pesticide hydrophobicity by way of machine / Albert J. Leo --
delivery parameter dependence on intermolecular forces / Marvin Charton --
QSARs from mathematical types : systemic habit of insecticides / D.A. Kleier --
Hydrophobicity and systemic actions of fungicidal triazoles and bleaching herbicidal compounds / Shizuya Tanaka, Masahiro Takahashi, Yuji Funaki, Kazuo Izumi, Hirotaka Takano, and Masakazu Miyakado --
The occurrence of delayed-type touch dermatitis in glossy insecticides / Philip S. Magee --
QSARs in environmental toxicology and chemistry : contemporary advancements / Joop L.M. Hermens and Henk J.M. Verhaar --
Noncongeneric structure-toxicity correlation utilizing fuzzy adaptive least-squares / I. Moriguchi, Q. Liu, H. Hirano, and S. Hirono --
Computer-aided molecular modeling and structure-activity analyses of recent antifungal tertiary amines / Chiyozo Takayama, Naoto Meki, Yasuyuki Kurita, and Hirotaka Takano --
QSARs and 3-dimensional form experiences of fungicidal azolylmethylcyclopentanols : molecular layout of novel fungicides metconazole and ipconazole / Hiroshi Chuman, Atsushi Ito, Toshihide Saishoji, and Satoru Kumazawa --
Structure-activity relationships of quinone and acridone photosystem II inhibitors / Wilfried Draber, Achim Trebst, and Walter Oettmeier --
The QSAR of insecticidal uncouplers / David M. Gange, Stephen Donovan, Ronald J. Lopata, and Kevin Henegar --
Quantitative structure-activity and molecular modeling reports of novel fungicides and herbicides having 1,2,4-thiadiazoline buildings / Akira Nakayama, Kenji Hagiwara, Sho Hashimoto, and Hideo Hosaka --
purposes of a brand new hydrophobicity parameter of amino acid facet chains to quantitative structure-activity analyses of oligopeptides / Miki Akamatsu, Tamio Ueno, and Toshio Fujita --
profitable software of the QSAR paradigm in discovery courses / Ernest L. Plummer --
Comparative QSAR : knowing hydrophobic interactions / Corwin Hansch --
functions of scaled rank-sum statistics in herbicide QSAR / Robert D. Clark, John J. Parlow, Lawrence H. Brannigan, Dora M. Schnur, and David L. Duewer --
Novel structure-activity insights from neural community versions / Tariq A. Andrea --
3-dimensional quantitative structure-activity research of steroidal and dibenzoylhydrazine-type ecdysone agonists / Yoshiaki Nakagawa, Bun-ichi Shimizu, Nobuhiro Oikawa, Miki Akamatsu, Keiichiro Nishimura, Norio Kurihara, Tamio Ueno, and Toshio Fujita --
comparability of classical QSAR and comparative molecular box research : towards lateral validations / Ki Hwan Kim --
Distance comparisons : a brand new method for reading three-d structure-activity relationships / Yvonne Connolly Martin.