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G Bock

Showing results (151-160 of 202) with videos related to

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Evolutionary Applications|July 29, 2016
Hybridization and extinctionMarco Todesco, Mariana A Pascual, Gregory L Owens, et al.
ACS Medicinal Chemistry Letters|August 18, 2022
Discovery and Optimization of Triazolopyrimidinone Derivatives as Selective NLRP3 Inflammasome InhibitorsDavid Harrison, Mark G Bock, John R Doedens, et al.
Journal of Medicinal Chemistry|December 10, 1993
Nanomolar-affinity, non-peptide oxytocin receptor antagonistsB E Evans, G F Lundell, K F Gilbert, et al.
Journal of Medicinal Chemistry|January 1, 1990
Cholecystokinin-A receptor ligands based on the kappa-opioid agonist tifluadomM G Bock, R M DiPardo, B E Evans, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1991
In vitro pharmacological profile of a novel structural class of oxytocin antagonistsD J Pettibone, B V Clineschmidt, E V Lis, et al.
Journal of Medicinal Chemistry|December 24, 1993
Development of 1,4-benzodiazepine cholecystokinin type B antagonistsM G Bock, R M DiPardo, B E Evans, et al.
Journal of Medicinal Chemistry|December 1, 1988
Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonistsB E Evans, K E Rittle, M G Bock, et al.
European Journal of Pharmacology|April 24, 1991
Bradykinin agonist activity of a novel, potent oxytocin antagonistD J Pettibone, B V Clineschmidt, E V Lis, et al.
Journal of Medicinal Chemistry|July 1, 1990
Cyclic hexapeptide oxytocin antagonists. Potency-, selectivity-, and solubility-enhancing modificationsR M Freidinger, P D Williams, R D Tung, et al.
Journal of Medicinal Chemistry|October 1, 1986
Cholecystokinin antagonists. Synthesis of asperlicin analogues with improved potency and water solubilityM G Bock, R M DiPardo, K E Rittle, et al.
Pageof 21

Showing results (151-160 of 202) with videos related to

Sort By:
Pageof 21
Evolutionary Applications|July 29, 2016
Hybridization and extinctionMarco Todesco, Mariana A Pascual, Gregory L Owens, et al.
ACS Medicinal Chemistry Letters|August 18, 2022
Discovery and Optimization of Triazolopyrimidinone Derivatives as Selective NLRP3 Inflammasome InhibitorsDavid Harrison, Mark G Bock, John R Doedens, et al.
Journal of Medicinal Chemistry|December 10, 1993
Nanomolar-affinity, non-peptide oxytocin receptor antagonistsB E Evans, G F Lundell, K F Gilbert, et al.
Journal of Medicinal Chemistry|January 1, 1990
Cholecystokinin-A receptor ligands based on the kappa-opioid agonist tifluadomM G Bock, R M DiPardo, B E Evans, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1991
In vitro pharmacological profile of a novel structural class of oxytocin antagonistsD J Pettibone, B V Clineschmidt, E V Lis, et al.
Journal of Medicinal Chemistry|December 24, 1993
Development of 1,4-benzodiazepine cholecystokinin type B antagonistsM G Bock, R M DiPardo, B E Evans, et al.
Journal of Medicinal Chemistry|December 1, 1988
Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonistsB E Evans, K E Rittle, M G Bock, et al.
European Journal of Pharmacology|April 24, 1991
Bradykinin agonist activity of a novel, potent oxytocin antagonistD J Pettibone, B V Clineschmidt, E V Lis, et al.
Journal of Medicinal Chemistry|July 1, 1990
Cyclic hexapeptide oxytocin antagonists. Potency-, selectivity-, and solubility-enhancing modificationsR M Freidinger, P D Williams, R D Tung, et al.
Journal of Medicinal Chemistry|October 1, 1986
Cholecystokinin antagonists. Synthesis of asperlicin analogues with improved potency and water solubilityM G Bock, R M DiPardo, K E Rittle, et al.
Pageof 21