Zobrazeno 1 - 10
of 16
pro vyhledávání: '"D O, Calligaro"'
Autor:
J S, Kennedy, F P, Bymaster, L, Schuh, D O, Calligaro, G, Nomikos, C C, Felder, M, Bernauer, B J, Kinon, R W, Baker, D, Hay, H J, Roth, M, Dossenbach, C, Kaiser, C M, Beasley, J H, Holcombe, M B, Effron, A, Breier
Publikováno v:
International journal of geriatric psychiatry. 16
Olanzapine (OLZ) is unique among currently available antipsychotic medications in its antagonism of a range of receptor systems including dopamine, norepinephrine, serotonin, acetylcholine, and histamine. Olanzapine's mechanistic complexity provides
Autor:
K, Rasmussen, D O, Calligaro, J F, Czachura, L J, Dreshfield-Ahmad, D C, Evans, S K, Hemrick-Luecke, M J, Kallman, W T, Kendrick, J D, Leander, D L, Nelson, C D, Overshiner, D B, Wainscott, M C, Wolff, D T, Wong, T A, Branchek, J M, Zgombick, Y C, Xu
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 294(2)
LY426965 [(2S)-(+)-1-cyclohexyl-4-[4-(2-methoxyphenyl)-1-piperazinyl]2-methyl- 2-phenyl-1-butanone monohydrochloride] is a novel compound with high affinity for the cloned human 5-hydroxytryptamine (HT)(1A) receptor (K(i) = 4.66 nM) and 20-fold or gr
Publikováno v:
Cellular signalling. 11(6)
Muscarinic agonists stimulated arachidonic acid release from 10- to 32-fold in Chinese hamster ovary (CHO) cells transfected with muscarinic M1, M3 and M5 receptor subtypes. Muscarinic agonists liberated arachidonic acid from the cAMP-coupled M2 and
Publikováno v:
The British journal of psychiatry. Supplement. (37)
Olanzapine, an atypical antipsychotic, has a broad receptor binding profile, which may account for its pharmacological effects in schizophrenia. In vitro receptor binding studies showed a high affinity for dopamine D2, D3, and D4 receptors; all 5-HT2
Autor:
M D, Swedberg, M J, Sheardown, P, Sauerberg, P H, Olesen, P D, Suzdak, K T, Hansen, F P, Bymaster, J S, Ward, C H, Mitch, D O, Calligaro, N W, Delapp, H E, Shannon
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 281(2)
Butylthio[2.2.2] ((+)-(S)-3-(4-(Butylthio)-1,2,5-thiadiazol-3-yl)-1-azabicyclo[2.2. 2] octane) is an agonist/antagonist at muscarinic receptors. The analgesic potential of butylthio[2.2.2] was assessed in the mouse by use of the grid-shock, tail-flic
Autor:
H E, Shannon, M J, Sheardown, F P, Bymaster, D O, Calligaro, N W, Delapp, J, Gidda, C H, Mitch, B D, Sawyer, P W, Stengel, J S, Ward, D T, Wong, P H, Olesen, P D, Suzdak, P, Sauerberg, M D, Swedberg
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 281(2)
Butylthio[2.2.2], ((+)-(S)-3-(4-butylthio-1,2,5-thiadiazol-3-yl)-1-azabicyclo[2.2.2] octane; LY297802/NNC11-1053) is a muscarinic receptor ligand which is equiefficacious to morphine in producing antinociception. In vitro, butylthio[2.2.2] had high a
Publikováno v:
The Journal of clinical psychiatry. 58
Classical (typical) antipsychotic drugs are in wide use clinically, but some patients do not respond at all to treatment, while in others, negative symptoms and cognitive deficits fail to respond. Also, these drugs often cause serious motor disturban
Autor:
C. H. Mitch, F. P. Bymaster, D. O. Calligaro, S. J. Quimby, B. D. Sawyer, H. E. Shannon, J. S. Ward, P. H. Olesen, P. Sauerberg, M. J. Sheardown, P. D. Suzdak, Novo Nordisk
Publikováno v:
Alzheimer’s and Parkinson’s Diseases ISBN: 9781475791471
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01a4252f01f408f12e8bd1dde0525080
https://doi.org/10.1007/978-1-4757-9145-7_66
https://doi.org/10.1007/978-1-4757-9145-7_66
Autor:
M M, Foreman, R W, Fuller, K, Rasmussen, D L, Nelson, D O, Calligaro, L, Zhang, J E, Barrett, R N, Booher, C J, Paget, M E, Flaugh
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 270(3)
(-)-LY293284, (-)-4R-6-acetyl-4-(di-n-propylamino)1,3,4,5- tetrahydrobenz[c,d]indole, is a conformationally restricted tryptamine derivative with an acetyl group serving as a protophilic substitution for the hydroxyl in serotonin (5-HT). In ligand di
Autor:
F P, Bymaster, D T, Wong, C H, Mitch, J S, Ward, D O, Calligaro, D D, Schoepp, H E, Shannon, M J, Sheardown, P H, Olesen, P D, Suzdak, M D, Swedberg, P, Sauerberg
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 269(1)
Xanomeline [3(3-hexyloxy-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetrahydro-1-me thylpyridine)] was evaluated in vivo in rat brain for effects on neurotransmitter turnover and inhibition of ex vivo binding of muscarinic radioligands. Xanomeline produced dose-