BDBM50441635 LICOAGRODIN

SMILES [#6]\[#6](-[#6])=[#6]\[#6]-c1cc(ccc1-[#8])[C@@]12[#8][C@@]34[#6@@H](-[#8]-c5c3ccc(-[#8])c5-[#6]\[#6]=[#6](\[#6])-[#6])-[#8]-c3cc(-[#8])ccc3-[#6@@H]4-[#6@@H]1-[#6](=O)-c1cc(-[#6]\[#6]=[#6](\[#6])-[#6])c(-[#8])cc1-[#8]2

InChI Key InChIKey=XXCXFEHYEHUBGX-UHFFFAOYSA-N

Data  1 IC50

  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 = 50441635   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Toho University

Curated by ChEMBL
LigandPNGBDBM50441635(LICOAGRODIN)
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibition of PTP1B (unknown origin) using p-nitrophenyl phosphate as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed