C. Hansch

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Substituent constants for correlation analysis in chemistry and biology

A. Leo, C. Hansch, 1979 .

Substituent constants for correlation analysis.

A. Leo, C. Hansch, S. D. Rockwell, 1977, Journal of medicinal chemistry.

p-σ-π Analysis. A Method for the Correlation of Biological Activity and Chemical Structure

C. Hansch, T. Fujita, 1964 .

Quantitative approach to biochemical structure-activity relationships

C. Hansch, 1969 .

Correlation of Biological Activity of Phenoxyacetic Acids with Hammett Substituent Constants and Partition Coefficients

R. M. Muir, C. Hansch, T. Fujita, 1962, Nature.

Linear free-energy relationship between partition coefficients and the aqueous solubility of organic liquids

C. Hansch, J. E. Quinlan, G. L. Lawrence, 1968 .

Partition coefficients and their uses

A. Leo, C. Hansch, David Elkins, 1971 .

The use of a hydrophobic bonding constant for structure-activity correlations.

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

A NEW SUBSTITUENT CONSTANT, PI, DERIVED FROM PARTITION COEFFICIENTS

C. Hansch, T. Fujita, J. Iwasa, 1964 .

Quantitative Structure‐Activity Relationships of the Benzodiazepines. A Review and Reevaluation.

C. Hansch, D. Hadjipavlou-Litina, 1995 .

QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS OF THE BENZODIAZEPINES. A REVIEW AND REEVALUATION

C. Hansch, D. Hadjipavlou-Litina, 1994 .

Quantitative structure-activity relationships and the unnamed science

C. Hansch, 1993 .

Chem-bioinformatics: comparative QSAR at the interface between chemistry and biology.

A. Leo, C. Hansch, D. Weininger, 2002, Chemical reviews.

Development of QSAR models using C-QSAR program: a regression program that has dual databases of over 21,000 QSAR models

C. Hansch, R. Verma, 2007 .

Matrix metalloproteinases (MMPs): chemical-biological functions and (Q)SARs.

C. Hansch, R. Verma, 2007, Bioorganic & medicinal chemistry.

The expanding role of quantitative structure-activity relationships (QSAR) in toxicology.

A. Leo, C. Hansch, D. Hoekman, 1995, Toxicology letters.

Comparative Quantitative Structure−Activity Relationship Studies on Anti-HIV Drugs

C. Hansch, A. Debnath, Hua Gao, 1999 .

Quantitative Structure–Activity Relationships of Heterocyclic Topoisomerase Iand II Inhibitors

C. Hansch, R. Verma, 2007 .

Comparative QSAR and the radical toxicity of various functional groups.

C. Hansch, C. Selassie, R. Verma, 2002, Chemical reviews.

Cytotoxicity of organic compounds against ovarian cancer cells: a quantitative structure-activity relationship study.

C. Hansch, R. Verma, 2006, Molecular pharmaceutics.

The physicochemical approach to drug design and discovery (QSAR)

Corwin Hansch, C. Hansch, 1981 .

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

Alan B. Forsythe, Stefan H. Unger, Corwin Hansch, 1973 .

Camptothecins: a SAR/QSAR study.

Corwin Hansch, C. Hansch, R. Verma, 2009, Chemical reviews.

Comparative QSAR: angiotensin II antagonists.

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

A survey of Hammett substituent constants and resonance and field parameters

Corwin Hansch, Albert J. Leo, A. Leo, 1991 .

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

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

A Survey of Hammett Substituent Constants and Resonance and Field Parameters

Corwin Hansch, Albert J. Leo, A. Leo, 1991 .

Comparative quantitative structure-activity relationship studies (QSAR) on non-benzodiazepine compounds binding to benzodiazepine receptor (BzR).

Rajni Garg, Corwin Hansch, C. Hansch, 2004, Chemical reviews.

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

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

"Aromatic" substituent constants for structure-activity correlations.

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

QSAR modeling of taxane analogues against colon cancer.

C. Hansch, R. Verma, 2010, European journal of medicinal chemistry.

Taxane Analogues against Lung Cancer: A Quantitative Structure–Activity Relationship Study

C. Hansch, R. Verma, 2009, Chemical biology & drug design.

Structure-activity relationships in antifungal agents. A survey.

C. Hansch, E. Lien, C Hansch, 1971, Journal of Medicinal Chemistry.

SUBSTITUENT CONSTANTS FOR CORRELATION ANALYSIS

Corwin Hansch, Albert J. Leo, A. Leo, 1977 .

′AROMATIC′ SUBSTITUENT CONSTANTS FOR STRUCTURE-ACTIVITY CORRELATIONS

A. Leo, C. Hansch, S. Unger, 1974 .

Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology

C. Hansch, Hua Gao, 1998 .

The use of substituent constants in the correlation of demethylation rates.

C. Hansch, A. Steward, J. Iwasa, 1965, Journal of medicinal chemistry.

Inhibition of chymotrypsin by alkyl phosphonates: a quantitative structure-activity analysis.

C. Hansch, C. Silipo, A. Vittoria, 1979, Archives of biochemistry and biophysics.

HIV-1 protease inhibitors: a comparative QSAR analysis.

Rajni Garg, Corwin Hansch, Alka Kurup, 2003, Current medicinal chemistry.

On the Mechanism of Action of Growth Regulators.

R. M. Muir, C. Hansch, 1953, Plant physiology.

The role of substituents in the hydrophobic bonding of phenols by serum and mitochondrial proteins.

C. Hansch, G. L. Lawrence, K. Kiehs, 1965, Journal of the American Chemical Society.

A QSAR review on melanoma toxicity.

C. Hansch, R. Verma, S. B. Mekapati, 2005, Bioorganic & medicinal chemistry.

Selection of a reference partitioning system for drug design work.

C. Hansch, M. Ames, R. Smith, 1975, Journal of pharmaceutical sciences.

A comparison of mutagenic and carcinogenic activities of aniline mustards.

A. Leo, C. Hansch, M. Shimkin, 1981, Journal of medicinal chemistry.

Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coin.

C. Hansch, L. Zhang, L. Zhang, 1995, SAR and QSAR in environmental research.

The effect of intramolecular bydrophobic bonding on partition coefficients

C. Hansch, S. M. Anderson, 1967 .

Investigation of DNA-binding properties of organic molecules using quantitative structure-activity relationship (QSAR) models.

C. Hansch, R. Verma, 2008, Journal of pharmaceutical sciences.

Directional nature of hydrophobic bonding in phenethanolamine N-methyl transferase inhibitors.

C. Hansch, W. R. Glave, 1972, Journal of medicinal chemistry.

The use of substituent constants in drug modification.

C. Hansch, 1968, Il Farmaco; edizione scientifica.

Structure-activity relationships in membrane-perturbing agents. Hemolytic, narcotic, and antibacterial compounds.

C. Hansch, W. R. Glave, 1971, Molecular pharmacology.

STRATEGY IN DRUG DESIGN, CLUSTER ANALYSIS AS AN AID IN THE SELECTION OF SUBSTITUENTS

C. Hansch, A. Forsythe, S. Unger, 1974 .

Comparative Quantitative Structure—Activity Relationship Studies (QSAR) on Non-Benzodiazepine Compounds Binding to Benzodiazepine Receptor (BzR)

C. Hansch, D. Hadjipavlou-Litina, R. Garg, 2004 .

GROWTH REGULATION BY ORGANIC COMPOUNDS.

R. M. Muir, C. Hansch, A. H. Gallup, 1949, Plant physiology.

QSAR of apoptosis induction in various cancer cells.

C. Hansch, R. Garg, B. Bonavida, 2003, Bioorganic & medicinal chemistry.

Structure-activity relationship in benzamides inhibiting alochol dehydrogenase.

C. Hansch, R. Sarma, K. H. Kim, 1973, Journal of the American Chemical Society.

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

C. Hansch, C Hansch, E Kutter, 1969, Journal of Medicinal Chemistry.

Chem-Bioinformatics: Comparative QSAR at the Interface Between Chemistry and Biology

A. Leo, C. Hansch, D. Weininger, 2010 .

Toward a quantitative comparative toxicology of organic compounds.

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

Hydrophobic effect in host-guest interactions. Hydrolysis of nitrophenyl carboxylates

C. Hansch, 1978 .

Binding of apolar molecules by serum albumin.

C. Hansch, C. Church, J. M. Vandenbelt, 1972, Journal of medicinal chemistry.

Thiocarbamates as plant growth regulators.

R. M. Muir, C. Hansch, J. Gally, 1961, Plant physiology.

Comparative QSAR of the sulfonamide function.

C. Hansch, 2003, Farmaco.

The Correlation of Biological Activity of Plant Growth Regulators and Chloromycetin Derivatives with Hammett Constants and Partition Coefficients

Toshio Fujita, R. M. Muir, Corwin Hansch, 1963 .

Cyclooxygenase (COX) inhibitors: a comparative QSAR study.

Rajni Garg, Corwin Hansch, Alka Kurup, 2003, Chemical reviews.

Drug research or the luck of the draw.

C. Hansch, 1974, Journal of chemical education.

Elucidation of structure-activity relationships for 2- or 6-substituted-5,8-dimethoxy-1,4-naphthoquinones.

C. Hansch, R. Verma, 2004, Bioorganic & medicinal chemistry.

Recent Advances in Biochemical QSAR

C. Hansch, 1978 .

Comprehensive medicinal chemistry : the rational design, mechanistic study & therapeutic application of chemical compounds

Corwin Hansch, C. Hansch, P. G. Sammes, 1990 .

Catalytic Synthesis of Heterocycles. VI. Dehydrocyclization of o-Alkylbenzenes to Indoles

C. Hansch, G. Helmkamp, 1951 .

Catalytic Synthesis of Heterocycles. V.1 Dehydrocyclization of Anils to Nitrogen Heterocycles

A. Leo, C. Hansch, D. Crosby, 1951 .

Catalytic Synthesis of Heterocycles.1 III. Benzofuran

C. Hansch, James N. Settle, William. Saltonstall, 1949 .

Comparative Quantitative Structure—Activity Relationship Studies on Anti-HIV Drugs

Rajni Garg, Corwin Hansch, C. Hansch, 2000 .

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.

Comparative QSAR analysis of estrogen receptor ligands.

C. Hansch, J. Katzenellenbogen, R. Garg, 1999, Chemical reviews.

Use of 13C NMR chemical shift as QSAR/QSPR descriptor.

Corwin Hansch, C. Hansch, R. Verma, 2011, Chemical reviews.

Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology.

Corwin Hansch, C. Hansch, Hua Gao, 1997, Chemical reviews.

Quantitative Structure–Activity Relationship – A Historical Perspective and the Future

C. Hansch, C. Selassie, C. Hansch, 2007 .

The role of hydrophobic properties of chemicals in promoting allosteric reactions.

C. Hansch, R. Verma, S. B. Mekapati, 2005, Bioorganic & medicinal chemistry.

Structure--activity relationships in thymidine phosphorylase inhibitors. A correlation using substituent constants and regression analysis.

C. Hansch, E. Coats, W. R. Glave, 1970, Journal of medicinal chemistry.

Antitumor structure-activity relations. Nitrosoureas vs. L-1210 leukemia.

A. Leo, C. Hansch, P. Y. Jow, 1980, Journal of medicinal chemistry.

SUBSTITUENT CONSTANTS FOR ALIPHATIC FUNCTIONS OBTAINED FROM PARTITION COEFFICIENTS.

C. Hansch, J. Iwasa, T. Fujita, 1965, Journal of medicinal chemistry.

Alkoxy derivatives of dodecaborate: discrete nanomolecular ions with tunable pseudometallic properties.

C. Hansch, M. Hawthorne, O. Farha, 2007, Angewandte Chemie.

Notes - A New Synthesis for Triphenylene

C. Hansch, C. Geiger, 1958 .

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.

Correlation analysis of ligand interactions with cycloamyloses

C. Hansch, C. Silipo, 1979 .

Influence of hydrophobic character on the relative rate of oxidation of drugs by rat liver microsomes.

C. Hansch, Y. Martin, 1971, Journal of medicinal chemistry.

The Vapor Phase Catalytic Synthesis of Thianaphthenes

C. Hansch, William A. Blondon, 1948 .

Chapter 33. Physicochemical Parameters in Drug Design

Corwin Hansch, C. Hansch, 1968 .

Role of hydrophobic effects in mechanistic QSAR

Corwin Hansch, Albert J. Leo, A. Leo, 1999 .

THE RELATIONSHIP OF STRUCTURE AND PLANT-GROWTH ACTIVITY OF SUBSTITUTED BENZOIC AND PHENOXYACETIC ACIDS.

R. M. Muir, C. Hansch, 1951, Plant physiology.

On the role of polarizability in QSAR.

C. Hansch, R. Verma, A. Kurup, 2005, Bioorganic & medicinal chemistry.

Chapter 34. The Use of Substituent Constants in Drug Design

C. Hansch, 1967 .

THE ORTHO EFFECT IN PLANT GROWTH-REGULATORS.

R. M. Muir, C. Hansch, 1950, 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.

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

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

Azulene Derivatives as Plant Growth Regulators

R. M. Muir, C. Hansch, 1961, Nature.

The structure-activity relationship in amides inhibiting photosynthesis.

C. Hansch, E. Deutsch, E. W. Deutsch, 1966, Bibliotek for laeger.

An approach toward the problem of outliers in QSAR.

Corwin Hansch, C. Hansch, R. Verma, 2005, Bioorganic & medicinal chemistry.

Linear free energy relations between partitioning solvent systems

Corwin Hansch, Albert J. Leo, A. Leo, 1971 .

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 antitumor aniline mustards.

A. Leo, C. Hansch, A. Panthananickal, 1978, Journal of medicinal chemistry.

Allosteric interactions and QSAR: on the role of ligand hydrophobicity.

C. Hansch, R. Garg, S. B. Mekapati, 2003, Bioorganic & medicinal chemistry.

QSAR of the inhibition of angiogenesis by TNP-470 and ovalicin analogues: another example of an allosteric interaction.

C. Hansch, S. B. Mekapati, 2001, Bioorganic & medicinal chemistry.

Structure-activity relationships of chemical mutagens and carcinogens.

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

A comparison between two polarizability parameters in chemical--biological interactions.

C. Hansch, R. Verma, 2005, Bioorganic & medicinal chemistry.

The structure-activity relationship in barbiturates and its similarity to that in other narcotics.

C. Hansch, S. M. Anderson, 1967, Journal of medicinal chemistry.

Quantitative Models of Steric Effects

Stefan H. Unger, Corwin Hansch, C. Hansch, 1977 .

Structure-activity relationship of chloramphenicols.

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

Dependence of Relative Sweetness on Hydrophobic Bonding

C. Hansch, E. W. Deutsch, 1966, Nature.

Model building in structure-activity relations. Reexamination of adrenergic blocking activity of .beta.-halo-.beta.-arylalkylamines

Stefan H. Unger, Corwin Hansch, C. Hansch, 1973 .

Alcohol dehydrogenase structure-activity relationships.

C. Hansch, R. Kerley, J. Schaeffer, 1972, The Journal of biological chemistry.

Understanding tubulin/microtubule-taxane interactions: a quantitative structure-activity relationship study.

C. Hansch, R. Verma, 2008, Molecular pharmaceutics.

Structure--activity correlations in the metabolism of drugs.

C. Hansch, E. Lien, F. Helmer, 1968, Archives of biochemistry and biophysics.

QUANTITATIVE RELATIONSHIPS OF STR U CTU R E-ACT1 Vl TY CYTOCHROME P-450*

C. Hansch, Litai Zhang, 1993 .

Quantitative structure-activity relationships of cytochrome P-450.

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

QSAR for the cytotoxicity of 2-alkyl or 2,6-dialkyl, 4-X-phenols: the nature of the radical reaction

Sanjay Kapur, Corwin Hansch, Rajeshwar P. Verma, 2002 .

Classical and Three-Dimensional QSAR in Agrochemistry

Toshio Fujita, Corwin Hansch, C. Hansch, 1995 .

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

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

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.

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.

Fibrinolytic congeners of benzoic and salicylic acid. A mathematical analysis of correlation between structure and activity.

C. Hansch, K. V. von Kaulla, 1970, Biochemical pharmacology.

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

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

20‐(S)‐Camptothecin Analogues as DNA Topoisomerase I Inhibitors: A QSAR Study

Corwin Hansch, C. Hansch, R. Verma, 2007, ChemMedChem.

Comparative QSAR studies on bibenzimidazoles and terbenzimidazoles inhibiting topoisomerase I.

C. Hansch, S. B. Mekapati, 2001, Bioorganic & medicinal chemistry.

Quantitative structure-activity relationships (QSAR) for 9-anilinoacridines: a comparative analysis.

C. Hansch, W. Denny, R. Garg, 1998, Chemico-biological interactions.

Catalytic Synthesis of Heterocycles. IX.1Dehydrocyclization of 2-Methyl-5-ethyl-4-pyridinethiol to 6-Methyl-5-azathianaphthene

C. Hansch, W. Carpenter, 1957 .

QSAR of anticancer compounds. Bis(11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides), bis(phenazine-1-carboxamides), and bis(naphthalimides).

C. Hansch, W. Denny, S. B. Mekapati, 2001, Bioorganic & medicinal chemistry.

Quantitative Relationships Between Lipophilic Character and Drug Metabolism

C. Hansch, 1972 .

3-substituted thianaphthenes.

C. Hansch, H. G. Lindwall, 1945, The Journal of organic chemistry.

Comparative QSAR: On the Toxicology of the Phenolic OH Moiety

Rajni Garg, Corwin Hansch, Alka Kurup, 2001, Critical reviews in toxicology.

QSAR of Cytochrome P450

Corwin Hansch, Alka Kurup, Suresh Babu Mekapati, 2004, Drug metabolism reviews.

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.

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.

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

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

Chemical Constitution as Related to Grwoth Regulator Action

A. R. Muir, C. Hansch, 1955 .

An Approach towards the Quantitative Structure–Activity Relationships of Caffeic Acid and its Derivatives

Corwin Hansch, C. Hansch, R. Verma, 2004, Chembiochem : a European journal of chemical biology.

The role of hydrophobic bonding in the binding of organic compounds by bovine hemoglobin.

C. Hansch, K. Kiehs, L. Moore, 1966, Biochemistry.

A comprehensive approach to database management of quantitative structure-activity relationships (QSAR) in chemistry and biology

Peng Li, Corwin Hansch, Albert J. Leo, 1994, 1994 Proceedings of the Twenty-Seventh Hawaii International Conference on System Sciences.

Comparative QSAR: Toward a Deeper Understanding of Chemicobiological Interactions.

Corwin Hansch, David Hoekman, C. Hansch, 1996, Chemical reviews.

The Dehydrocyclization Reaction.

C. Hansch, 1953 .

Homolytic constants in the correlation of chloramphenicol structure with activity.

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

The use of substituent constants in the quantitative treatment of hapten-antibody interaction.

C. Hansch, E. Kutter, Eberhard Kutter, 1969, Archives of biochemistry and biophysics.

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

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

α-Chymotrypsin: A Case Study of Substituent Constants and Regression Analysis in Enzymic Structure—Activity Relationships

Corwin Hansch, C. Hansch, Eugene A. Coats, 1970 .

Comparative QSAR studies on substituted bis-(acridines) and bis-(phenazines)-carboxamides: a new class of anticancer agents.

C. Hansch, W. Denny, R. Garg, 2000, Bioorganic & medicinal chemistry.

Classical and three-dimensional QSAR in agrochemistry : developed from a symposium sponsored by the Division of Agrochemicals at the 208th National Meeting of the American Chemical Society, Washington, DC, August 21-25, 1994

Toshio Fujita, Corwin Hansch, C. Hansch, 1995 .

A QSAR study on influenza neuraminidase inhibitors.

Corwin Hansch, C. Hansch, R. Verma, 2006, Bioorganic & medicinal chemistry.

QSAR and ADME.

Corwin Hansch, Alka Kurup, Suresh Babu Mekapati, 2004, Bioorganic & medicinal chemistry.

On the toxicity of phenols to fast growing cells. A QSAR model for a radical-based toxicity

Sanjay Kapur, Corwin Hansch, Rajeshwar P. Verma, 1999 .

Comparative QSAR Analysis of Estrogen Receptor Ligands

Rajni Garg, Corwin Hansch, John A. Katzenellenbogen, 1999 .

Use of quantitative structure-activity relationships (QSAR) in drug design (review)

C. Hansch, C. Hansch, 1980, Pharmaceutical Chemistry Journal.

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

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

The QSAR paradigm in the design of less toxic molecules.

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

Additive-constitutive character of partition coefficients

A. Leo, C. Hansch, D. Nikaitani, 1972 .

Correlation of chaotropic effects of haloacetates with the hydrophobic parameter .

C. Hansch, N. Cornell, 1972, Archives of biochemistry and biophysics.

Role of the benzyl moiety in biochemical and pharmacological processes.

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

Extrathermodynamic approach to the study of the adsorption of organic compounds by macromolecules

C. Hansch, F. Helmer, 1968 .

Catalytic Synthesis of Heterocycles. VIII.1Dehydrocyclization ofo-Ethylbenzenethiols to Thianaphenes.2

Corwin Hansch, C. Hansch, Beno. Schmidhalter, 1956 .

SYNTHESIS OF 6-SUBSTITUTED THIANAPHTHENES

C. Hansch, Beno. Schmidhalter, 1955 .

Comparative QSAR analysis of 5alpha-reductase inhibitors.

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

A QSAR study for the cytotoxic activities of taxoids against macrophage (MPhi)-like cells.

C. Hansch, R. Verma, 2009, European journal of medicinal chemistry.

Relationship between lipophilic character and anesthetic activity.

C. Hansch, W. R. Glave, 1972, Journal of pharmaceutical sciences.

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.

THE USE OF SUBSTITUENT CONSTANTS IN THE ANALYSIS OF THE STRUCTURE--ACTIVITY RELATIONSHIP IN PENICILLIN DERIVATIVES.

C. Hansch, A. Steward, C HANSCH, 1964, Journal of medicinal chemistry.

On the structure of medicinal chemistry.

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

Organic chemistry : an outline : problems and answers

C. Hansch, G. Helmkamp, 1959 .

Dependence of hydrophobicity of apolar molecules on their molecular volume.

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

Understanding human rhinovirus infections in terms of QSAR.

C. Hansch, R. Verma, 2007, Virology.

Enzyme Study As a Source of Strategy in Drug Design

C. Hansch, 1975 .

Chemical Toxicity on HeLa Cells.

Corwin Hansch, C. Hansch, R. Verma, 2006, Current medicinal chemistry.

Taxane Analogues against Breast Cancer: A Quantitative Structure–Activity Relationship Study

C. Hansch, R. Verma, 2008, ChemMedChem.

Larvicidal activities of some organotin compounds on mosquito larvae: a QSAR study.

C. Hansch, R. Verma, 2009, European journal of medicinal chemistry.

Combating the threat of anthrax: a quantitative structure-activity relationship approach.

C. Hansch, R. Verma, 2008, Molecular pharmaceutics.

Comparative QSAR studies on PAMPA/modified PAMPA for high throughput profiling of drug absorption potential with respect to Caco-2 cells and human intestinal absorption

Corwin Hansch, Rajeshwar P. Verma, Cynthia Rachel Selassie, 2007, J. Comput. Aided Mol. Des..

Correlation of ratios of drug metabolism by microsomal subfractions with partition coefficients.

C. Hansch, E. Lien, 1968, Journal of pharmaceutical sciences.

QSAR of HIV inhibitors

Corwin Hansch, C. Hansch, Litai Zhang, 1992 .

NITRATION OF o-ACETYLAMINOETHYLBENZENE

C. Hansch, 1955 .

Comparative QSAR and radical toxicology: the aromatic CH2OH moiety

C. Hansch, R. Garg, 2001 .

Induction of Cytochrome P450 by Barbiturates in Chick Embryo Hepatocytes: A Quantitative Structure-Activity Analysis

C. Hansch, P. Sinclair, J. Sinclair, 1990 .

Hydrophobic interaction of small molecules with alpha-chymotrypsin.

C. Hansch, R. Smith, 1973, Biochemistry.

Searching for allosteric effects via QSAR. Part II.

C. Hansch, R. Garg, S. B. Mekapati, 2003, Bioorganic & medicinal chemistry.

Structure-activity relationship of aniline mustards acting against B-16 melanoma in mice.

A. Leo, C. Hansch, A. Panthananickal, 1979, Journal of medicinal chemistry.

Chemical-biological interactions in human.

C. Hansch, R. Verma, S. B. Mekapati, 2005, Bioorganic & medicinal chemistry.

Comparative QSAR Analysis of 5α‐Reductase Inhibitors

Rajni Garg, Corwin Hansch, Alka Kurup, 2000 .

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

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

Partition coefficients and the structure-activity relationship of the anesthetic gases.

C. Hansch, P. Y. Jow, C. Silipo, 1975, Journal of medicinal chemistry.

Hydrophobicity and central nervous system agents: on the principle of minimal hydrophobicity in drug design.

A. Leo, C. Hansch, C. Hansch, 1987, Journal of pharmaceutical sciences.

The structure-activity relationship of inhibitors of serotonin uptake and receptor binding

Corwin Hansch, Jonathan Caldwell, C. Hansch, 1991, J. Comput. Aided Mol. Des..

Lipophilic character and biological activity of drugs. II. The parabolic case.

C. Hansch, C. Hansch, C Hansch, 1973, Journal of pharmaceutical sciences.

Overcoming tumor drug resistance with C2-modified 10-deacetyl-7-propionyl cephalomannines: a QSAR study.

Corwin Hansch, C. Hansch, R. Verma, 2009, Molecular pharmaceutics.

QSAR of Chemical Polarizability and Nerve Toxicity. 2

Corwin Hansch, Alka Kurup, C. Hansch, 2003, J. Chem. Inf. Comput. Sci..

QSAR in cancer chemotherapy.

C. Hansch, 1979, Il Farmaco; edizione scientifica.

The advent and evolution of QSAR at Pomona College

Corwin Hansch, C. Hansch, 2011, J. Comput. Aided Mol. Des..

Camptothecins: a SAR/QSAR study.

C. Hansch, R. Verma, 2009, Chemical reviews.

On the Role of Polarizability in Chemical-Biological Interactions

Corwin Hansch, Alka Kurup, Suresh Babu Mekapati, 2003, J. Chem. Inf. Comput. Sci..

Comparative QSAR: Understanding Hydrophobic Interactions

C. Hansch, 1995 .

Percutaneous penetration of drugs: a quantitative structure-permeability relationship study.

N el Tayar, B Testa, A. Leo, 1991, Journal of pharmaceutical sciences.

Taxane Analogues against Lung Cancer: A Quantitative Structure–Activity Relationship Study

C. Hansch, R. Verma, 2009, Chemical biology & drug design.

Quantitative structure-activity relationships of chymotrypsin-ligand interactions: An analysis of interactions in ϱ3 space

C. Hansch, C. Silipo, A. Vittoria, 1979 .

QSAR OF THE INHIBITION OF CHYMOTRYPSIN BY ALKYL PHOSPHONATES

C. Hansch, C. Silipo, A. Vittoria, 1980 .

Quantitative structure-activity relationship of chymotrypsin-ligand interactions.

C. Hansch, C. Silipo, A. Vittoria, 1977, Journal of medicinal chemistry.

Quantitative structure-activity relationships of chymotrypsin. On the predictive value of correlation equations.

C. Hansch, C. Silipo, A. Vittoria, 1977, Journal of Medicinal Chemistry.

QUANTITATIVE STRUCTURE-ACTIVITY RELATIONS OF CHYMOTRYPSIN. THE PREDICTIVE VALUE OF CORRELATION EQUATIONS

C. Hansch, C. Silipo, A. Vittoria, 1977 .

PARTITION COEFFICIENTS AND THE STRUCTURE-ACTIVITY RELATIONSHIP OF THE ANESTHETIC GASES

C. Hansch, P. Y. Jow, C. Silipo, 1975 .

STRUCTURE-ACTIVITY RELATIONSHIP OF CHLORAMPHENICOLS

C. Hansch, E. R. Garrett, C. Won, 1973 .

THE USE OF SUBSTITUENT CONSTANTS AND REGRESSION ANALYSIS IN THE STUDY OF ENZYMATIC REACTION MECHANISMS.

C. Hansch, R. Smith, E. W. Deutsch, 1965, Journal of the American Chemical Society.