BDBM50008096 CHEMBL2372414::cyclo(Ppa-Phe(N3)-Phe-Val-Asn-Cys)-Pro-Lys-D-Tyr-NH2

SMILES CC(C)[C@@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccc(cc2)N=[N+]=[N-])NC(=O)C2(CCCC2)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@H](Cc1ccc(O)cc1)C(N)=O

InChI Key InChIKey=FBOAXWIBFYZMMM-UHFFFAOYSA-N

Data  2 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50008096   

TargetVasopressin V1a receptor(Rat)
University of Sherbrooke

Curated by ChEMBL
LigandPNGBDBM50008096(CHEMBL2372414 | cyclo(Ppa-Phe(N3)-Phe-Val-Asn-Cys)...)
Affinity DataKd:  35nMAssay Description:Negative log of Kd for Vasopressin V1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetVasopressin V1a receptor(Rat)
University of Sherbrooke

Curated by ChEMBL
LigandPNGBDBM50008096(CHEMBL2372414 | cyclo(Ppa-Phe(N3)-Phe-Val-Asn-Cys)...)
Affinity DataKd:  36nMAssay Description:Binding potency against Vasopressin V1 receptor in rat liver cells.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed