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Название: Classical and Three-Dimensional QSAR in Agrochemistry
Авторы: Hansch C., Fujita T.
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.