Content: Status of QSAR at the end of the twentieth century / Corwin Hansch and Toshio Fujita —
Quantitative structure-activity analysis and database-aided bioisosteric structural transformation procedure as methodologies of agrochemical design / Toshio Fujita —
Hydrophobicity parameter of heteroaromatic compounds derived from various partitioning systems / Chisako Yamagami and Toshio Fujita —
Theoretical estimation of octanol-water partition coefficient for organophosphorus pesticides / Toshiyuki Katagi, Masakazu Miyakado, Chiyozo Takayama, and Shizuya Tanaka —
The calculation of pesticide hydrophobicity by computer / Albert J. Leo —
Transport parameter dependence on intermolecular forces / Marvin Charton —
QSARs from mathematical models : systemic behavior of pesticides / D.A. Kleier —
Hydrophobicity and systemic activities of fungicidal triazoles and bleaching herbicidal compounds / Shizuya Tanaka, Masahiro Takahashi, Yuji Funaki, Kazuo Izumi, Hirotaka Takano, and Masakazu Miyakado —
The incidence of delayed-type contact dermatitis in modern pesticides / Philip S. Magee —
QSARs in environmental toxicology and chemistry : recent developments / Joop L.M. Hermens and Henk J.M. Verhaar —
Noncongeneric structure-toxicity correlation using fuzzy adaptive least-squares / I. Moriguchi, Q. Liu, H. Hirano, and S. Hirono —
Computer-aided molecular modeling and structure-activity analyses of new antifungal tertiary amines / Chiyozo Takayama, Naoto Meki, Yasuyuki Kurita, and Hirotaka Takano —
QSARs and three-dimensional shape studies of fungicidal azolylmethylcyclopentanols : molecular design 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 studies of novel fungicides and herbicides having 1,2,4-thiadiazoline structures / Akira Nakayama, Kenji Hagiwara, Sho Hashimoto, and Hideo Hosaka —
Applications of a new hydrophobicity parameter of amino acid side chains to quantitative structure-activity analyses of oligopeptides / Miki Akamatsu, Tamio Ueno, and Toshio Fujita —
Successful application of the QSAR paradigm in discovery programs / Ernest L. Plummer —
Comparative QSAR : understanding hydrophobic interactions / Corwin Hansch —
Applications 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 network models / Tariq A. Andrea —
Three-dimensional quantitative structure-activity analysis 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 —
Comparison of classical QSAR and comparative molecular field analysis : toward lateral validations / Ki Hwan Kim —
Distance comparisons : a new strategy for examining three-dimensional structure-activity relationships / Yvonne Connolly Martin.