Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C HANSCH

Showing results (51-60 of 197) with videos related to

Pageof 20
Sort By:
Journal of Medicinal Chemistry|July 1, 1973
On model building in structure-activity relationships. A reexamination of adrenergic blocking activity of beta-halo-beta-arylalkylaminesS H Unger, C Hansch
Molecular Pharmacology|May 1, 1971
Structure-activity relationships in membrane-perturbing agents. Hemolytic, narcotic, and antibacterial compoundsC Hansch, W R Glave
Journal of Medicinal Chemistry|January 1, 1972
Directional nature of hydrophobic bonding in phenethanolamine N-methyl transferase inhibitorsC Hansch, W R Glave
Il Farmaco; Edizione Scientifica|July 1, 1979
QSAR of alkyl pyridinecarbonyldithiocarbazates as uncouplers of oxidative phosphorylationK H Kim, C Hansch
Journal of Pharmaceutical Sciences|January 1, 1973
Lipophilic character and biological activity of drugs. II. The parabolic caseC Hansch, J M Clayton
Journal of Agricultural and Food Chemistry|March 1, 1981
Quantitative structure-activity relationship of phenyl N-methylcarbamate inhibition of acetylcholinesteraseA 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 diseaseM Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)|October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunctionF 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 glycinatesA Carotti, C Raguseo, C Hansch
Chemical Reviews|December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitorsA Kurup, R Garg, C Hansch
Pageof 20

Showing results (51-60 of 197) with videos related to

Sort By:
Pageof 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-arylalkylaminesS H Unger, C Hansch
Molecular Pharmacology|May 1, 1971
Structure-activity relationships in membrane-perturbing agents. Hemolytic, narcotic, and antibacterial compoundsC Hansch, W R Glave
Journal of Medicinal Chemistry|January 1, 1972
Directional nature of hydrophobic bonding in phenethanolamine N-methyl transferase inhibitorsC Hansch, W R Glave
Il Farmaco; Edizione Scientifica|July 1, 1979
QSAR of alkyl pyridinecarbonyldithiocarbazates as uncouplers of oxidative phosphorylationK H Kim, C Hansch
Journal of Pharmaceutical Sciences|January 1, 1973
Lipophilic character and biological activity of drugs. II. The parabolic caseC Hansch, J M Clayton
Journal of Agricultural and Food Chemistry|March 1, 1981
Quantitative structure-activity relationship of phenyl N-methylcarbamate inhibition of acetylcholinesteraseA 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 diseaseM Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)|October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunctionF 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 glycinatesA Carotti, C Raguseo, C Hansch
Chemical Reviews|December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitorsA Kurup, R Garg, C Hansch
Pageof 20