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185213-03-0

185213-03-0 Structure

185213-03-0 Structure
IdentificationBack Directory
[Name]

Butabindide oxalate
[CAS]

185213-03-0
[Synonyms]

[S-(R*,R*)]-1-(2-Amino-1-oxobutyl)-N-butyl-2,3-dihydro-1H-indole-2-carboxamide ethanedioate
[Molecular Formula]

C19H27N3O6
[MOL File]

185213-03-0.mol
[Molecular Weight]

393.434
Chemical PropertiesBack Directory
[Melting point ]

142 °C
[storage temp. ]

Desiccate at -20°C
[solubility ]

Soluble to 100 mM in water and to 100 mM in DMSO
[form ]

Powder
Hazard InformationBack Directory
[Description]

Butabindide is a potent inhibitor of cholecystokinin-inactivating peptidase/tripeptidyl peptidase 2 (CCK-inactivating peptidase/TPP-2; Ki = 7 nM). It is selective for CCK-inactivating peptidase/TPP-2 over a panel of serine proteases (Kis = >1 μM) as well as CCK receptors (Kis = >0.1 mM). Butabindide (0.1-100 μM) increases levels of CCK octapeptide (Item Nos. 24404 | 23371) in depolarized rat cerebral cortex slices. In vivo, butabindide inhibits CCK-inactivating peptidase/TPP-2 in mouse liver and brain (ID50s = 1.1 and 6.8 mg/kg, respectively). It also enhances CCK octapeptide-induced delay in gastric emptying and reduces food intake in mice.
[storage]

Desiccate at -20°C
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