YM471, a vasopressin V1A/V2 antagonist, bound rat oxytocin receptors with a Ki of 31.0 nM, much lower affinity than for V1A and V2 receptors.
In plain wordsIn lab tests, a vasopressin-blocking compound bound oxytocin receptors much more weakly than vasopressin receptors.
- Peptide
- Oxytocin
- Outcome
- Not applicableYM471 binding affinity (Ki) at the oxytocin receptor
- Study
ratn: not reported in source
Receptor binding with rat receptors- Outcome group
- Receptor activity and mechanism · Pharmacology
Measurements
- Ki
- 31 nM
- YM471, rat oxytocin receptor
Source sentences
YM471 exhibited much lower affinity for rat vasopressin V(1B) and oxytocin receptors, with K(i) values of 10.5 microM and 31.0 nM, respectively.
1 context sentence(design, population, supporting numbers)
The pharmacologic profile of YM471 ((Z)-4'-[4,4-difluoro-5-[2-(4-dimethylaminopiperidino)-2-oxoethylidene]-2,3,4,5-tetrahydro-1H-1-benzoazepine-1-carbonyl]-2-phenylbenzanilide monohydrochloride), a novel potent vasopressin V(1A) and V(2) receptor antagonist, was investigated using several in vitro a…
In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.