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Chemical Reviews
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November 20, 2001
Chem-bioinformatics and QSAR: a review of QSAR lacking positive hydrophobic terms
C Hansch, A Kurup, R Garg, et al.
Physiological Chemistry and Physics
|
January 1, 1974
Parabolic hydrophobic inhibition of alpha-chymotrypsin
B N Smith, C Hansch, T P Poindexter
Mutation Research
|
July 1, 1992
Mutagenicity of quinolines in Salmonella typhimurium TA100. A QSAR study based on hydrophobicity and molecular orbital determinants
A K Debnath, R L de Compadre, C Hansch
Biochemical Pharmacology
|
February 15, 1986
Induction of cytochrome P-450 by alcohols and 4-substituted pyrazoles. Comparison of structure-activity relationships
J Sinclair, N W Cornell, L Zaitlin, et al.
Chemical Reviews
|
December 26, 2001
Comparative QSAR: angiotensin II antagonists
A Kurup, R Garg, D J Carini, et al.
Il Farmaco; Edizione Scientifica
|
December 1, 1987
Concanavalin X-phenyl beta-D-glucopyranoside interactions. A molecular graphics-QSAR analysis
M Recanatini, T E Klein, R Langridge, et al.
Bioorganic & Medicinal Chemistry
|
February 24, 2001
Mechanism of toxicity of esters of caffeic and dihydrocaffeic acids
B Etzenhouser, C Hansch, S Kapur, et al.
Journal of Medicinal Chemistry
|
July 1, 1982
Comparison of the inhibition of Escherichia coli and Lactobacillus casei dihydrofolate reductase by 2,4-diamino-5-(substituted-benzyl)pyrimidines: quantitative structure-activity relationships, X-ray crystallography, and computer graphics in structure-activity analysis
C Hansch, R Li, J M Blaney, et al.
Chemical Reviews
|
December 26, 2001
Comparative QSAR analysis of estrogen receptor ligands
H Gao, J A Katzenellenbogen, R Garg, et al.
Journal of Medicinal Chemistry
|
September 1, 1975
Calculation of hydrophobic constant (log P) from pi and f constants
A Leo, P Y Jow, C Silipo, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 197) with videos related to
Sort By:
Page
of 20
Chemical Reviews
|
November 20, 2001
Chem-bioinformatics and QSAR: a review of QSAR lacking positive hydrophobic terms
C Hansch, A Kurup, R Garg, et al.
Physiological Chemistry and Physics
|
January 1, 1974
Parabolic hydrophobic inhibition of alpha-chymotrypsin
B N Smith, C Hansch, T P Poindexter
Mutation Research
|
July 1, 1992
Mutagenicity of quinolines in Salmonella typhimurium TA100. A QSAR study based on hydrophobicity and molecular orbital determinants
A K Debnath, R L de Compadre, C Hansch
Biochemical Pharmacology
|
February 15, 1986
Induction of cytochrome P-450 by alcohols and 4-substituted pyrazoles. Comparison of structure-activity relationships
J Sinclair, N W Cornell, L Zaitlin, et al.
Chemical Reviews
|
December 26, 2001
Comparative QSAR: angiotensin II antagonists
A Kurup, R Garg, D J Carini, et al.
Il Farmaco; Edizione Scientifica
|
December 1, 1987
Concanavalin X-phenyl beta-D-glucopyranoside interactions. A molecular graphics-QSAR analysis
M Recanatini, T E Klein, R Langridge, et al.
Bioorganic & Medicinal Chemistry
|
February 24, 2001
Mechanism of toxicity of esters of caffeic and dihydrocaffeic acids
B Etzenhouser, C Hansch, S Kapur, et al.
Journal of Medicinal Chemistry
|
July 1, 1982
Comparison of the inhibition of Escherichia coli and Lactobacillus casei dihydrofolate reductase by 2,4-diamino-5-(substituted-benzyl)pyrimidines: quantitative structure-activity relationships, X-ray crystallography, and computer graphics in structure-activity analysis
C Hansch, R Li, J M Blaney, et al.
Chemical Reviews
|
December 26, 2001
Comparative QSAR analysis of estrogen receptor ligands
H Gao, J A Katzenellenbogen, R Garg, et al.
Journal of Medicinal Chemistry
|
September 1, 1975
Calculation of hydrophobic constant (log P) from pi and f constants
A Leo, P Y Jow, C Silipo, et al.
Page
of 20