Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ben E. Evans"'
Autor:
Heidi T. Orme, Jixin Wang, Joseph J. Salata, Ben E. Evans, Nancy K. Jurkiewicz, Michael C. Sanguinetti
Publikováno v:
Molecular Pharmacology. 54:220-230
The slowly activating delayed rectifier K+ current, IKs, is an important modulator of cardiac action potential repolarization. Here, we describe a novel benzodiazepine, [L-364,373 [(3-R)-1, 3-dihydro-5-(2-fluorophenyl)-3-(1H-indol-3-ylmethyl)-1-methy
Autor:
Kenneth E. Rittle, Raymond S.L. Chang, Daniel F. Veber, Willie L. Whitter, Mark G. Bock, Roger M. Freidinger, Paul S. Anderson, Ben E. Evans, Victor J. Lotti, Robert M. DiPardo
Publikováno v:
Journal of Controlled Release. 21:73-80
Cholecystokinin (CCK) is a polypeptide hormone which occurs in numerous molecular forms at various sites throughout the peripheral and central nervous systems. The wide range of physiological responses which have been attributed to CCK has stimulated
Autor:
Kenneth E. Rittle, Daniel F. Veber, Roger M. Freidinger, Ben E. Evans, Raymond S. L. Chang, Willie L. Whitter, Victor J. Lotti, Mark G. Bock, Robert M. DiPardo, Tsing-Bau Chen
Publikováno v:
Journal of Medicinal Chemistry. 33:450-455
Tifluadom, a kappa-opioid agonist and cholecystokinin-A (CCK-A) receptor antagonist, was utilized as a model to prepare a series of 2-(aminomethyl)- and 3-(aminomethyl)-1,4-benzodiazepines. These compounds were tested in vitro as inhibitors of the bi
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461372103
There is currently a need for new therapeutic agents for treating preterm labor which could offer improved safety and efficacy beyond what has been achieved with the widely employed beta-mimetics. In this regard, the longstanding hypothesis of oxytoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f63e38f7cd0ad48cc7503813d25af160
https://doi.org/10.1007/978-1-4615-4871-3_61
https://doi.org/10.1007/978-1-4615-4871-3_61
Autor:
James B. Hoffman, Jill M. Erb, Kevin F. Gilbert, Daniel F. Veber, Roger M. Freidinger, Mark G. Bock, Robert M. DiPardo, Ben E. Evans, James L. Leighton, George F. Lundell, Douglas J. Pettibone, Bradley V. Clineschmidt, Willie L. Whitter, Roger D. Tung, Peter D. Williams, N. P. Gould, Debra S. Perlow
Publikováno v:
Peptides ISBN: 9789401090681
Peptides 1992
Peptides 1992 ISBN: 9789401046466
Peptides 1992
Peptides 1992 ISBN: 9789401046466
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::571f6301248c7a3a088649e1aeae6c39
https://doi.org/10.1007/978-94-010-9066-7_17
https://doi.org/10.1007/978-94-010-9066-7_17
Autor:
Ben E. Evans, James L. Leighton, Kenneth E. Rittle, Kevin F. Gilbert, George F. Lundell, Norman P. Gould, Doug W. Hobbs, Robert M. DiPardo, Daniel F. Veber, Douglas J. Pettibone, Bradley V. Clineschmidt, Paul S. Anderson, Roger M. Freidinger
Publikováno v:
Journal of medicinal chemistry. 35(21)
The first nonpeptide antagonists of the neurohypophyseal hormone, oxytocin (OT) are described. Derivatives of the spiroindenepiperidine ring system, these compounds include L-366,509, an orally bioavailable OT antagonist with good in vivo duration. T
Autor:
Ben E. Evans, Paul S. Anderson, Marcia E. Christy, C. Dylion Colton, David C. Remy, Kenneth E. Rittle, Edward L. Engelhardt
Publikováno v:
The Journal of Organic Chemistry. 44:3127-3135
Autor:
Victor J. Lotti, Kenneth E. Rittle, Robert M. DiPardo, Raymond S. L. Chang, Ben E. Evans, Mark G. Bock, Roger M. Freidinger
Publikováno v:
Journal of Medicinal Chemistry. 31:264-268
Autor:
Daniel F. Veber, Ben E. Evans, Carl F. Homnick, J. Hirshfield, Kenneth E. Rittle, James P. Springer
Publikováno v:
The Journal of Organic Chemistry. 50:4615-4625
Autor:
James P. Springer, Tsing-Bau Chen, Robert M. DiPardo, Roger M. Freidinger, Paul J. Kling, Paul S. Anderson, D. J. Cerino, K. A. Kunkel, Daniel F. Veber, J. Hirshfield, W. L. Whitter, Kenneth E. Rittle, Ben E. Evans, Victor J. Lotti, George F. Lundell, Mark G. Bock, Raymond S.L. Chang
Publikováno v:
Journal of Medicinal Chemistry. 31:2235-2246
3-(Acylamino)-5-phenyl-2H-1,4-benzodiazepines, antagonists of the peptide hormone cholecystokinin (CCK), are described. Developed by reasoned modification of the known anxiolytic benzodiazepines, these compounds provide highly potent, orally effectiv