null

SMILES CC(C)C[C@@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CCSSC[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCNC(=O)c1ccccc1N)C(=O)NCC(O)=O

InChI Key InChIKey=IIIHGTMRSVLZBO-NKUVHBIJSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50342029   

TargetVasopressin V2 receptor(Homo sapiens (Human))
INSERM

Curated by ChEMBL
LigandPNGBDBM50342029(2-((S)-2-((S)-1-((4R,7S,10S,13S,16S)-7-(2-amino-2-...)copy SMILEScopy InChI
Affinity DataKi:  4.92E+3nMAssay Description:Displacement of [3H]AVP from human vasopressin V2 receptor expressed CHO cells after 60 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B60GJPubMed