BDBM50247413 CHEMBL486199::Cyclo(ALYSYRVE)

SMILES [#6]-[#6](-[#6])-[#6]-[#6@H]-1-[#7]-[#6](=O)-[#6@@H](-[#6])-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccc(-[#8])cc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#8])-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccc(-[#8])cc2)-[#7]-[#6]-1=O)-[#6](-[#6])-[#6]

InChI Key InChIKey=PUEQDDJWNAEWTB-CBWMTVFUSA-N

Data  1 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50247413   

TargetProlactin receptor(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL
LigandPNGBDBM50247413(CHEMBL486199 | Cyclo(ALYSYRVE))
Affinity DataKd:  3.00E+3nMAssay Description:Binding affinity to human prolactin receptor extracelluar binding domain by surface plasmon responseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed