BDBM50005611 CHEMBL3234641

SMILES [H][C@@]1(O[C@H]2CC[C@@]3(C)[C@@]([H])(CC[C@]4(C)[C@]3([H])CC=C3[C@]5([H])CC(C)(C)CC[C@@]5(CC[C@@]43C)C(=O)O[C@@H]3O[C@H](CNC(=O)c4ccccc4C(O)=O)[C@@H](O)[C@H](O)[C@H]3O)C2(C)C)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Key InChIKey=OTORWUPHQWRVJN-UHFFFAOYSA-N

Data  2 IC50

  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 = 50005611   

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

Curated by ChEMBL
LigandPNGBDBM50005611(CHEMBL3234641)
Affinity DataIC50: 1.72E+4nMAssay Description:Inhibition of recombinant PTP1B (unknown origin) using p-nitrophenyl phosphate as substrate assessed as inhibition of release of p-nitrophenol preinc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2015
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
North-West University

Curated by ChEMBL
LigandPNGBDBM50005611(CHEMBL3234641)
Affinity DataIC50: 3.05E+4nMAssay Description:Inhibition of TCPTP (unknown origin) using p-nitrophenyl phosphate as substrate assessed as inhibition of release of p-nitrophenol preincubated for 1...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2015
Entry Details Article
PubMed