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W C Randall

Showing results (141-150 of 164) with videos related to

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Naunyn-Schmiedeberg'S Archives of Pharmacology|August 1, 1987
Pharmacological profile of a new potent and specific alpha 2-adrenoceptor antagonist, L-657,743D J Pettibone, B V Clineschmidt, V J Lotti, et al.
Journal of Medicinal Chemistry|July 23, 1993
Sulfonylmethanesulfonamide inhibitors of carbonic anhydraseT H Scholz, J M Sondey, W C Randall, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1989
Chemical synthesis of echistatin, a potent inhibitor of platelet aggregation from Echis carinatus: synthesis and biological activity of selected analogsV M Garsky, P K Lumma, R M Freidinger, et al.
The American Journal of Physiology|September 5, 1998
Ablation of posterior atrial ganglionated plexus potentiates sympathetic tachycardia to behavioral stressD C Randall, D R Brown, S G Li, et al.
Journal of Medicinal Chemistry|October 16, 1992
4-substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, R L Smith, et al.
Journal of Medicinal Chemistry|April 1, 1987
Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitorsG S Ponticello, M B Freedman, C N Habecker, et al.
Journal of Medicinal Chemistry|August 7, 1992
Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, J D Prugh, et al.
Journal of Medicinal Chemistry|December 1, 1985
N-(1,3,4,6,7,12b-hexahydro-2H-benzo[b]furo[2,3-a]quinolizin -2-yl)-N- methyl-2-hydroxyethane-sulfonamide: a potent and selective alpha 2-adrenoceptor antagonistJ R Huff, P S Anderson, J J Baldwin, et al.
Protein Science : a Publication of the Protein Society|January 1, 1994
Positions of His-64 and a bound water in human carbonic anhydrase II upon binding three structurally related inhibitorsG M Smith, R S Alexander, D W Christianson, et al.
Journal of Medicinal Chemistry|August 1, 1983
Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivativesH W Williams, E Eichler, W C Randall, et al.
Pageof 17

Showing results (141-150 of 164) with videos related to

Sort By:
Pageof 17
Naunyn-Schmiedeberg'S Archives of Pharmacology|August 1, 1987
Pharmacological profile of a new potent and specific alpha 2-adrenoceptor antagonist, L-657,743D J Pettibone, B V Clineschmidt, V J Lotti, et al.
Journal of Medicinal Chemistry|July 23, 1993
Sulfonylmethanesulfonamide inhibitors of carbonic anhydraseT H Scholz, J M Sondey, W C Randall, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1989
Chemical synthesis of echistatin, a potent inhibitor of platelet aggregation from Echis carinatus: synthesis and biological activity of selected analogsV M Garsky, P K Lumma, R M Freidinger, et al.
The American Journal of Physiology|September 5, 1998
Ablation of posterior atrial ganglionated plexus potentiates sympathetic tachycardia to behavioral stressD C Randall, D R Brown, S G Li, et al.
Journal of Medicinal Chemistry|October 16, 1992
4-substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, R L Smith, et al.
Journal of Medicinal Chemistry|April 1, 1987
Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitorsG S Ponticello, M B Freedman, C N Habecker, et al.
Journal of Medicinal Chemistry|August 7, 1992
Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, J D Prugh, et al.
Journal of Medicinal Chemistry|December 1, 1985
N-(1,3,4,6,7,12b-hexahydro-2H-benzo[b]furo[2,3-a]quinolizin -2-yl)-N- methyl-2-hydroxyethane-sulfonamide: a potent and selective alpha 2-adrenoceptor antagonistJ R Huff, P S Anderson, J J Baldwin, et al.
Protein Science : a Publication of the Protein Society|January 1, 1994
Positions of His-64 and a bound water in human carbonic anhydrase II upon binding three structurally related inhibitorsG M Smith, R S Alexander, D W Christianson, et al.
Journal of Medicinal Chemistry|August 1, 1983
Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivativesH W Williams, E Eichler, W C Randall, et al.
Pageof 17