-
Devazepide (L-364,718, MK-329) is
benzodiazepine drug, but with
quite different actions from most benzodiazepines,
lacking affinity for
GABAA receptors...
- 3-bromocamphor-8-sulfonic acid was used in the
synthesis of
enantiopure devazepide.
Camphorsulfonic acid is also
being used for the
synthesis of quinolines...
- the
GABAA modulatory action of the
classical benzodiazepines, such as
devazepide and tifluadom,
however these have not been
included in the list below...
- receptors.
Selective CCKA
receptor antagonists such as
lorglumide and
devazepide have been
developed both for
their anti-ulcer
effects and as potential...
-
detrothyronine (INN)
detumomab (INN)
deuruxolitinib (INN)
devapamil (INN)
devazepide (INN) Dexacen-4
Dexacidin Dexacort Dexair dexamethasone acefurate (INN)...
- and
despite older selective CCKA
antagonists such as
lorglumide and
devazepide having had only
limited success in
trials and
ultimately never making...
- S2CID 25951941. Josselyn, S. A.; Franco, V. P.; Vaccarino, F. J. (1996-01-01). "
Devazepide, a CCKA
receptor antagonist,
impairs the
acquisition of
conditioned reward...
-
Galcanezumab Agonists:
Cholecystokinin Antagonists:
Amiglumide Asperlicin Devazepide Dexloxiglumide Lintitript Lorglumide Loxiglumide Pranazepide Proglumide...
- Flo G,
Daenens P,
Decuypere E, Kühn E, Van
Boven M (December 1995). "
Devazepide reverses the
anorexic effect of
simmondsin in the rat". The
Journal of...
- 1200x
selectivity over CCKB, CAS# 130408-77-4
Proglumide Lorglumide Devazepide Dexloxiglumide Asperlicin SR-27897 IQM-95333 JNJ-17156516 Cholecystokinin...
