C Hansch

发表

Comparative QSAR in toxicology: examples from teratology and cancer chemotherapy of aniline mustards.

C. Hansch, L. Zhang, C Hansch, 1995, Critical reviews in toxicology.

Structure-activity relationship in the auxin activity of mono-substituted phenylacetic acids.

R. M. Muir, R M Muir, C. Hansch, 1967, Plant physiology.

FURTHER EVIDENCE FOR A CHEMICAL REACTION BETWEEN PLANT GROWTH-REGULATORS AND A PLANT SUBSTRATE.

R. M. Muir, R M Muir, R L Metzenberg, 1951, Plant physiology.

Comparison of parameters currently used in the study of structure-activity relationships.

A. Leo, C. Hansch, C Hansch, 1969, Journal of medicinal chemistry.

Radical toxicity of phenols: A reference point for obtaining perspective in the formulation of QSAR

C. Hansch, R. Garg, S. Kapur, 2001, Medicinal research reviews.

Structure-activity correlations for antibacterial agents on gram-positive and gram-negative cells.

C. Hansch, E. Lien, C Hansch, 1968, Journal of medicinal chemistry.

Structure-activity relationships in antifungal agents. A survey.

C. Hansch, E. Lien, C Hansch, 1971, Journal of medicinal chemistry.

Strategy in drug design. Cluster analysis as an aid in the selection of substituents.

A B Forsythe, S H Unger, C Hansch, 1973, Journal of medicinal chemistry.

The linear free-energy relationship between partition coefficients and the binding and conformational perturbation of macromolecules by small organic compounds.

C. Hansch, C Hansch, F Helmer, 1968, Biochemistry.

Calculation of hydrophobic constant (log P) from pi and f constants.

C Silipo, A. Leo, C. Hansch, 1975, Journal of medicinal chemistry.

The correlation of localization rates of benzeneboronic acids in brain and tumor tissue with substituent constants.

C. Hansch, A. Steward, J. Iwasa, 1965, Molecular pharmacology.

An analysis of the structure-activity relationship in the adrenergic blocking activity of the beta-haloalkylamines.

C. Hansch, E. Lien, C Hansch, 1968, Biochemical pharmacology.

Steric parameters in drug design. Monoamine oxidase inhibitors and antihistamines.

C. Hansch, C Hansch, E Kutter, 1969, Journal of medicinal chemistry.

On the structure of medicinal chemistry.

C. Hansch, C Hansch, 1976, Journal of medicinal chemistry.

Role of the benzyl moiety in biochemical and pharmacological processes.

C. Hansch, C Hansch, R Kerley, 1970, Journal of medicinal chemistry.

The parabolic dependence of drug action upon lipophilic character as revealed by a study of hypnotics.

C. Hansch, A. Steward, C Hansch, 1968, Journal of medicinal chemistry.

Comparative QSAR analysis of estrogen receptor ligands.

C. Hansch, Hua Gao, J. Katzenellenbogen, 1999, Chemical reviews.

Quantitative structure-activity relationships of cytochrome P-450.

C. Hansch, L. Zhang, C Hansch, 1993, Drug metabolism reviews.

The QSAR paradigm in the design of less toxic molecules.

C. Hansch, C Hansch, 1984, Drug metabolism reviews.

"Aromatic" substituent constants for structure-activity correlations.

S H Unger, A. Leo, C. Hansch, 1973, Journal of medicinal chemistry.

Chem-bioinformatics and QSAR: a review of QSAR lacking positive hydrophobic terms.

C. Hansch, R. Garg, A. Kurup, 2001, Chemical reviews.

The structure-activity relationship of skin carcinogenicity of aromatic hydrocarbons and heterocycles.

L Zhang, C. Hansch, A. Shusterman, 1992, Chemico-biological interactions.

Formulation of de novo substituent constants in correlation analysis: inhibition of dihydrofolate reductase by 2,4-diamino-5-(3,4-dichlorophenyl)-6-substituted pyrimidines.

C Silipo, C. Hansch, E. E. Steller, 1975, Journal of pharmaceutical sciences.

Dependence of hydrophobicity of apolar molecules on their molecular volume.

A. Leo, C. Hansch, P. Y. Jow, 1976, Journal of medicinal chemistry.

Correlation analysis of Baker's studies on enzyme inhibition. 1. Guanine deaminase, xanthine oxidase, dihydrofolate reductase, and complement.

C Silipo, C. Hansch, C Hansch, 1976, Journal of medicinal chemistry.

Structure-activity relationship of chloramphenicols.

C. Hansch, C. Won, C Hansch, 1973, Journal of medicinal chemistry.

Toward a quantitative comparative toxicology of organic compounds.

E Novellino, C Silipo, A. Leo, 1989, Critical reviews in toxicology.

Correlation analysis. Its application to the structure-activity relationship of triazines inhibiting dihydrofolate reductase.

C Silipo, C. Hansch, C Hansch, 1975, Journal of the American Chemical Society.

Passive permeation of organic compounds through biological tissue: a non-steady-state theory.

C. Hansch, J. Penniston, D L Bentley, 1969, Molecular pharmacology.

Quantitative structure-activity relationships of antineoplastic drugs: nitrosoureas and triazenoimidazoles.

C. Hansch, C Hansch, N Smith, 1972, Cancer chemotherapy reports.

Structure-activity relationships of chemical mutagens and carcinogens.

C. Hansch, C Hansch, 1991, The Science of the total environment.

Comparative QSAR: angiotensin II antagonists.

C. Hansch, R. Garg, A. Kurup, 2001, Chemical reviews.

Comparative QSAR analysis of 5alpha-reductase inhibitors.

C. Hansch, R. Garg, A. Kurup, 2000, Chemical reviews.

Quantitative structure-activity relationship of reversible dihydrofolate reductase inhibitors. Diaminotriazines.

C Silipo, C. Hansch, C Hansch, 1974, Journal of medicinal chemistry.

Comparative QSAR study of tyrosine kinase inhibitors.

C. Hansch, R. Garg, A. Kurup, 2001, Chemical reviews.