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

W Daly

Showing results (361-370 of 385) with videos related to

Pageof 39
Sort By:
Drug Development Research|March 15, 2013
Activation and Desensitization of Rat A<sub>3</sub>-Adenosine Receptors by Selective Adenosine Derivatives and Xanthine-7-RibosidesKyung-Sun Park, Carsten Hoffmann, Hea Ok Kim, et al.
Toxicon : Official Journal of the International Society on Toxinology|October 14, 2008
Indolizidine 239Q and quinolizidine 275I. Major alkaloids in two Argentinian bufonid toads (Melanophryniscus)John W Daly, H Martin Garraffo, Thomas F Spande, et al.
Neurochemical Research|April 1, 1990
Procaine isothiocyanate: an irreversible inhibitor of the specific binding of [3H]batrachotoxinin-A benzoate to sodium channelsC R Creveling, M E Bell, T R Burke, et al.
Beilstein Journal of Organic Chemistry|September 21, 2011
Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptorsSoushi Kobayashi, Naoki Toyooka, Dejun Zhou, et al.
Journal of Medicinal Chemistry|August 1, 1989
Sulfur-containing 1,3-dialkylxanthine derivatives as selective antagonists at A1-adenosine receptorsK A Jacobson, L Kiriasis, S Barone, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2007
Synthesis of poison-frog alkaloids 233A, 235U, and 251AA and their inhibitory effects on neuronal nicotinic acetylcholine receptorsNaoki Toyooka, Soushi Kobayashi, Dejun Zhou, et al.
Journal of Natural Products|December 28, 2005
A revised structure for alkaloid 235C isolated from skin extracts of mantellid (Mantella) frogs of MadagascarN Rabe Andriamaharavo, Marta Andriantsiferana, Paul A Stevenson, et al.
Journal of Medicinal Chemistry|March 1, 1991
Effect of fluorine substitution on the adrenergic properties of 3-(tert-butylamino)-1-(3,4-dihydroxyphenoxy)-2-propanolA Adejare, J Y Nie, D Hebel, et al.
Biochemical Pharmacology|July 15, 1990
Pumiliotoxin alkaloids: a new class of sodium channel agentsJ W Daly, F Gusovsky, E T McNeal, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1977
Perhydrohistrionicotoxin: a potential ligand for the ion conductance modulator of the acetylcholine receptorA T Eldefrawi, M E Eldefrawi, E X Albuquerque, et al.
Pageof 39

Showing results (361-370 of 385) with videos related to

Sort By:
Pageof 39
Drug Development Research|March 15, 2013
Activation and Desensitization of Rat A<sub>3</sub>-Adenosine Receptors by Selective Adenosine Derivatives and Xanthine-7-RibosidesKyung-Sun Park, Carsten Hoffmann, Hea Ok Kim, et al.
Toxicon : Official Journal of the International Society on Toxinology|October 14, 2008
Indolizidine 239Q and quinolizidine 275I. Major alkaloids in two Argentinian bufonid toads (Melanophryniscus)John W Daly, H Martin Garraffo, Thomas F Spande, et al.
Neurochemical Research|April 1, 1990
Procaine isothiocyanate: an irreversible inhibitor of the specific binding of [3H]batrachotoxinin-A benzoate to sodium channelsC R Creveling, M E Bell, T R Burke, et al.
Beilstein Journal of Organic Chemistry|September 21, 2011
Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptorsSoushi Kobayashi, Naoki Toyooka, Dejun Zhou, et al.
Journal of Medicinal Chemistry|August 1, 1989
Sulfur-containing 1,3-dialkylxanthine derivatives as selective antagonists at A1-adenosine receptorsK A Jacobson, L Kiriasis, S Barone, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2007
Synthesis of poison-frog alkaloids 233A, 235U, and 251AA and their inhibitory effects on neuronal nicotinic acetylcholine receptorsNaoki Toyooka, Soushi Kobayashi, Dejun Zhou, et al.
Journal of Natural Products|December 28, 2005
A revised structure for alkaloid 235C isolated from skin extracts of mantellid (Mantella) frogs of MadagascarN Rabe Andriamaharavo, Marta Andriantsiferana, Paul A Stevenson, et al.
Journal of Medicinal Chemistry|March 1, 1991
Effect of fluorine substitution on the adrenergic properties of 3-(tert-butylamino)-1-(3,4-dihydroxyphenoxy)-2-propanolA Adejare, J Y Nie, D Hebel, et al.
Biochemical Pharmacology|July 15, 1990
Pumiliotoxin alkaloids: a new class of sodium channel agentsJ W Daly, F Gusovsky, E T McNeal, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1977
Perhydrohistrionicotoxin: a potential ligand for the ion conductance modulator of the acetylcholine receptorA T Eldefrawi, M E Eldefrawi, E X Albuquerque, et al.
Pageof 39