BDBM50182708 CHEMBL3819005

SMILES [#6]-[#6](-[#6])-[#6]-[#6](-[#6]-[#6](=O)-[#7]-[#6](-[#6]-c1ccsc1)-[#6](-[#7])=O)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#7]-[#6](=O)-c1ccc(\[#6]=[#6]-2/[#6]-[#6]-[#7]-[#6]-[#6]-2)cc1

InChI Key InChIKey=HTCLFQGNCUDTLN-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 = 50182708   

TargetCyclin-A2/Cyclin-dependent kinase 2(Human)
University of South Carolina

Curated by ChEMBL
LigandPNGBDBM50182708(CHEMBL3819005)
Affinity DataIC50: 9.16E+3nMAssay Description:Inhibition of recombinant human CDK2/cyclin A2 using fluoresceinyl-Ahx-Pro-Val-Lys-Arg-Arg-Leu-Phe-Gly as substrate incubated for 45 mins by fluoresc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/27/2017
Entry Details Article
PubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Human)
University of South Carolina

Curated by ChEMBL
LigandPNGBDBM50182708(CHEMBL3819005)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human CDK4/cyclin D1 using fluoresceinyl-AhxPro-Val-Lys-Arg-Arg-Leu-(3ClPhe)-Gly as substrate incubated for 45 mins by fluo...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/27/2017
Entry Details Article
PubMed