Target
Rat vasopressin-neurophysin
Ligand
BDBM81892
Substrate
n/a
Ki
240±n/a nM
Comments
PDSP_1041
Citation
 Pettibone, DJClineschmidt, BVLis, EVReiss, DRTotaro, JAWoyden, CJBock, MGFreidinger, RMTung, RDVeber, DF In vitro pharmacological profile of a novel structural class of oxytocin antagonists. J Pharmacol Exp Ther 256:304-8 (1991) [PubMed] 
Target
Name:
Rat vasopressin-neurophysin
Synonyms:
Rat preprovasopressin-neurophysin | VASOPRESSIN V1
Type:
Enzyme Catalytic Domain
Mol. Mass.:
2826.33
Organism:
RAT
Description:
VASOPRESSIN V1 0 RAT::Q6LEI5
Residue:
26
Sequence:
MLNTTLSACFLSLLALTSACYFQNCP
  
Inhibitor
Name:
BDBM81892
Synonyms:
Cyclo[L-Pro-D-Phe-L-Ile-1,6-didehydro-D-Pyz-N-methyl-D-Phe-] | J440.774A | L-366,706
Type:
Small organic molecule
Emp. Form.:
C35H44N6O5
Mol. Mass.:
628.7611
SMILES:
CCC(C)C1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H]2CCCN2C(=O)C(Cc2ccccc2)N(C)C(=O)[C@H]2CCC=NN2C1=O |c:44|
Structure:
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