Zobrazeno 1 - 10
of 132
pro vyhledávání: '"D. J. Triggle"'
Autor:
D J, Triggle
Publikováno v:
Pharmaceutica Acta Helvetiae. 74:287-290
Pharmacological receptors are typically defined by their selectivity of ligand recognition, including where appropriate stereoselectivity of interaction. It is increasingly clear that receptors may, in fact, be promiscuous species. This promiscuity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::878f00136481c4f73e0cf9fe58c00b53
https://doi.org/10.1016/s0031-6865(99)00054-0
https://doi.org/10.1016/s0031-6865(99)00054-0
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08d897ee644c3ba01e958fb3c8028532
https://doi.org/10.1002/chin.199103223
https://doi.org/10.1002/chin.199103223
Autor:
S. D. Jablonski, P. Singh, Philip Abraham, J. B. Pitner, Y. W. Kwon, Frank I. Carroll, D. J. Triggle
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5d320849632760be24e5f4b11b2692c
https://doi.org/10.1002/chin.199242189
https://doi.org/10.1002/chin.199242189
Publikováno v:
Cleveland Clinic Journal of Medicine. 59:617-627
The calcium-channel antagonists represent three separate structural categories of drugs. They share a common action--the blockade of calcium-ion flow through one specific type of calcium channel. The chemical heterogeneity of these agents is reflecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8142012f216a7c67c4cb07b1491f11e
https://doi.org/10.3949/ccjm.59.6.617
https://doi.org/10.3949/ccjm.59.6.617
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 261:H1979-H1987
To examine the status of ATP-sensitive K+ (K+ATP) channels and 1,4-dihydropyridine-sensitive Ca2+ (Ca2+DHP) channels during experimental cardiac failure, we have measured the radioligand binding properties of [3H]glyburide and [3H]PN 200 110, respect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f0a83fb2f28a1ac328e602d243bd059
https://doi.org/10.1152/ajpheart.1991.261.6.h1979
https://doi.org/10.1152/ajpheart.1991.261.6.h1979
Publikováno v:
Journal of Medicinal Chemistry. 34:3164-3171
Synthesis, radioligand binding, and pharmacologic activities of a series of muscarinic receptor ligands including and related to azaprophen (6-methyl-6-azabicyclo[3.2.1]octan-3 alpha-ol 2,2-diphenylpropionate, 1) have been measured to determine activ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7de0377c91870005f191fc9bde1e01
https://doi.org/10.1021/jm00115a003
https://doi.org/10.1021/jm00115a003
Autor:
D J, Triggle
Publikováno v:
IDrugs : the investigational drugs journal. 2(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fc9d4b04b29b9433ad6847fa1100c61
https://pubmed.ncbi.nlm.nih.gov/16113970
https://pubmed.ncbi.nlm.nih.gov/16113970
Autor:
D P, Rotella, D J, Triggle
Publikováno v:
IDrugs : the investigational drugs journal. 3(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c223bcef0ca6b4044846b3bf18cdb820
https://pubmed.ncbi.nlm.nih.gov/16047233
https://pubmed.ncbi.nlm.nih.gov/16047233
Publikováno v:
Biochemical pharmacology. 62(7)
Binding of the class III antiarrhythmic agent azimilide to brain, heart, and other organ receptors was assessed by standard radioligand binding techniques. In a survey of 60 receptors, azimilide at 10 microM inhibited binding by more than 50% at sero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f5baf32dbf904392673ca9b537564d16
https://pubmed.ncbi.nlm.nih.gov/11543723
https://pubmed.ncbi.nlm.nih.gov/11543723
Autor:
P, Angeli, D J, Triggle
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 55(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::15a267bd1fb762142aec52e0992a12cb
https://pubmed.ncbi.nlm.nih.gov/10983290
https://pubmed.ncbi.nlm.nih.gov/10983290