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Journal of Medicinal Chemistry
|
July 1, 1973
On model building in structure-activity relationships. A reexamination of adrenergic blocking activity of beta-halo-beta-arylalkylamines
S H Unger, C Hansch
Molecular Pharmacology
|
May 1, 1971
Structure-activity relationships in membrane-perturbing agents. Hemolytic, narcotic, and antibacterial compounds
C Hansch, W R Glave
Journal of Medicinal Chemistry
|
January 1, 1972
Directional nature of hydrophobic bonding in phenethanolamine N-methyl transferase inhibitors
C Hansch, W R Glave
Il Farmaco; Edizione Scientifica
|
July 1, 1979
QSAR of alkyl pyridinecarbonyldithiocarbazates as uncouplers of oxidative phosphorylation
K H Kim, C Hansch
Journal of Pharmaceutical Sciences
|
January 1, 1973
Lipophilic character and biological activity of drugs. II. The parabolic case
C Hansch, J M Clayton
Journal of Agricultural and Food Chemistry
|
March 1, 1981
Quantitative structure-activity relationship of phenyl N-methylcarbamate inhibition of acetylcholinesterase
A Goldblum, M Yoshimoto, C Hansch
Chemico-Biological Interactions
|
August 1, 1997
A comparative QSAR analysis of acetylcholinesterase inhibitors currently studied for the treatment of Alzheimer's disease
M Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)
|
October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunction
F J Pirozzolo, E C Hansch
Chemico-Biological Interactions
|
January 1, 1985
Quantitative structure-activity relationships of cysteine hydrolases. Ficin hydrolysis of X-phenyl-N-methanesulfonyl glycinates
A Carotti, C Raguseo, C Hansch
Chemical Reviews
|
December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitors
A Kurup, R Garg, C Hansch
Page
of 20
Search research articles
Search
Showing results (51-60 of 197) with videos related to
Sort By:
Page
of 20
Journal of Medicinal Chemistry
|
July 1, 1973
On model building in structure-activity relationships. A reexamination of adrenergic blocking activity of beta-halo-beta-arylalkylamines
S H Unger, C Hansch
Molecular Pharmacology
|
May 1, 1971
Structure-activity relationships in membrane-perturbing agents. Hemolytic, narcotic, and antibacterial compounds
C Hansch, W R Glave
Journal of Medicinal Chemistry
|
January 1, 1972
Directional nature of hydrophobic bonding in phenethanolamine N-methyl transferase inhibitors
C Hansch, W R Glave
Il Farmaco; Edizione Scientifica
|
July 1, 1979
QSAR of alkyl pyridinecarbonyldithiocarbazates as uncouplers of oxidative phosphorylation
K H Kim, C Hansch
Journal of Pharmaceutical Sciences
|
January 1, 1973
Lipophilic character and biological activity of drugs. II. The parabolic case
C Hansch, J M Clayton
Journal of Agricultural and Food Chemistry
|
March 1, 1981
Quantitative structure-activity relationship of phenyl N-methylcarbamate inhibition of acetylcholinesterase
A Goldblum, M Yoshimoto, C Hansch
Chemico-Biological Interactions
|
August 1, 1997
A comparative QSAR analysis of acetylcholinesterase inhibitors currently studied for the treatment of Alzheimer's disease
M Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)
|
October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunction
F J Pirozzolo, E C Hansch
Chemico-Biological Interactions
|
January 1, 1985
Quantitative structure-activity relationships of cysteine hydrolases. Ficin hydrolysis of X-phenyl-N-methanesulfonyl glycinates
A Carotti, C Raguseo, C Hansch
Chemical Reviews
|
December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitors
A Kurup, R Garg, C Hansch
Page
of 20