Zobrazeno 1 - 10
of 13
pro vyhledávání: '"S F, Pong"'
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
Publikováno v:
Experientia. 29:527-529
Yoduro de 2, 9-dimetilo-carbolinio (DMCI) y no sus metabolitos inhibio la enzyma monoamino oxidasa y elevo14C-serotonia en el corazon e higado, pero no en el cerebro de ratas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c78cd7cf4d2ef91e273f98be8e6ab7c
https://doi.org/10.1007/bf01926643
https://doi.org/10.1007/bf01926643
Publikováno v:
The Journal of pharmacy and pharmacology. 37(11)
Dantrolene sodium (Dantrium) has antiarrhythmic activity in addition to its direct-acting skeletal muscle relaxant activity. Dantrolene sodium exerts its skeletal muscle relaxant action by reducing Ca2+ release for sarcoplasmic reticulum. The mechani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862156de3f719a0c68d1aac7b6091333
https://pubmed.ncbi.nlm.nih.gov/2867170
https://pubmed.ncbi.nlm.nih.gov/2867170
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 273(2)
The oral analgesic activities (ED50's) of 15 NSAIDs were determined in the phenylquinone-induced writhing test in mice. ED50 values (mg/kg) were: acetylsalicylic acid (182), fenclofenac (168), phenylbutazone (129), ibuprofen (82.2), diflunisal (55.6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e588c0661c14c746aff15d59a2d24bd
https://pubmed.ncbi.nlm.nih.gov/3873924
https://pubmed.ncbi.nlm.nih.gov/3873924
Autor:
S F, Pong, S S, Pelosi, F L, Wessels, C N, Yu, R H, Burns, R E, White, D R, Anthony, K O, Ellis, G C, Wright, R L, White
Publikováno v:
Arzneimittel-Forschung. 33(10)
A series of 5-phenyl-2-furamidines has been synthesized and evaluated for antidepressant activities. Substitution in the phenyl ring with a nitro (4) or an amino (12) group in the ortho-position resulted in an increase in antidepressant activity. Bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31f4915d6485ec2f56d18b7dd5610d26
https://pubmed.ncbi.nlm.nih.gov/6140016
https://pubmed.ncbi.nlm.nih.gov/6140016
Autor:
S F, Pong, L T, Graham
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 220(2)
Intravitreal injection of GABA- and glycine-antagonists had specific and reversible effects on the ERG of rats. For example, picrotoxin induced characteristic rhythmic potentials. The effect was common to other GABA-antagonists, such as bicuculline,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e040923d91ff8dff23a97ab8ac5de72f
https://pubmed.ncbi.nlm.nih.gov/952584
https://pubmed.ncbi.nlm.nih.gov/952584
Autor:
L. T. Graham, S. F. Pong
Publikováno v:
Experientia. 30(8)
Nous avons observe que l'injection de la 6-hydroxydopamine dans l'humeur vitree des rats adaptes a la lumiere bloquait le retablissement de la sensibilite retinale pendant l'adaptation a l'obscurite subsequente au traitement. Il est possible que cett
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ac559fb43d5b698cc1da48bb6cf27b
https://pubmed.ncbi.nlm.nih.gov/4413924
https://pubmed.ncbi.nlm.nih.gov/4413924
Autor:
L T Graham, S F Pong
Publikováno v:
The Journal of pharmacy and pharmacology. 30(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae5086b50b533d52af2ef0a675f18bd8
https://pubmed.ncbi.nlm.nih.gov/26755
https://pubmed.ncbi.nlm.nih.gov/26755
Publikováno v:
The Journal of pharmacy and pharmacology. 34(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e8da87ed506f640e0b17f21658b4f87
https://pubmed.ncbi.nlm.nih.gov/6121897
https://pubmed.ncbi.nlm.nih.gov/6121897
Publikováno v:
Arzneimittel-Forschung. 38(1)
5-[5-(4-Chlorophenyl-2-furanyl)]dihydro-2(3H)-furanone (F-1044), a nonsteroidal antiinflammatory drug related to orpanoxin, lacks the usual acid moiety of such agents. F-1044 had antiinflammatory activity equivalent to ibuprofen's and orpanoxin's in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1469384faf503b885fc1c5faa54efc7a
https://pubmed.ncbi.nlm.nih.gov/3365279
https://pubmed.ncbi.nlm.nih.gov/3365279