Reaction Details  Report a problem with these data
Target
Promotilin
Ligand
BDBM50004656
Substrate
n/a
Ki
158.49±n/a nM
Comments
PDSP_467
Citation
 Clark, MJ; Wright, T; Bertrand, PP; Bornstein, JC; Jenkinson, KM; Verlinden, M; Furness, JB Erythromycin derivatives ABT 229 and GM 611 act on motilin receptors in the rabbit duodenum. Clin Exp Pharmacol Physiol 26:242-5 (1999) [PubMed]  Article
Target
Name:
Promotilin
Synonyms:
MLN | MOTI_RABIT | Motilin | Promotilin
Type:
Enzyme Catalytic Domain
Mol. Mass.:
14668.99
Organism:
RABBIT
Description:
Motilin 0 RABBIT::P27114
Residue:
133
Sequence:
MVSRKAVAALLLVHVTAMLASQTEAFVPIFTYSELQRMQERERNRGHKKSLSVQQRSDAAAAPRPAEPTLEEENGRMQLTAPVEIGMRMNSRQLEKYRAALEAAERAVHPDAPSRPCWPAGGESGWSGEPSPT
  
Inhibitor
Name:
BDBM50004656
Synonyms:
(2-Carbamoyloxy-ethyl)-trimethyl-ammonium | (2-Carbamoyloxyethyl)trimethylammonium chloride | (2-Hydroxyethyl)trimethyl ammonium chloride carbamate | (2-Hydroxyethyl)trimethylammonium chloride carbamate | (carbachol)(2-Carbamoyloxy-ethyl)-trimethyl-ammonium | 2-((Aminocarbonyl)oxy)-N,N,N-trimethylethanaminium chloride | 2-((Aminocarbonyl)oxy)-N,N,N-trimethylethanaminum chloride | 2-(carbamoyloxy)-N,N,N-trimethylethanaminium | 2-(carbamoyloxy)-N,N,N-trimethylethanaminium chloride | CARBACHOL | CARBASTAT | CHEMBL14 | Carbachol chloride | Carbamylcholine | Choline carbamate chloride | Choline chloride, carbamate | Choline chlorine carbamate | Karbachol | Karbamoylcholin chlorid | MIOSTAT
Type:
Small organic molecule
Emp. Form.:
C6H15N2O2
Mol. Mass.:
147.195
SMILES:
C[N+](C)(C)CCOC(N)=O
Structure:
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