BDBM50629592 CHEMBL5415967

SMILES O=C(Nc1ccc(cc1)N1CCNCC1)c1n[nH]cc1Nc1cc(ncn1)C1CC1

InChI Key InChIKey=SEAAQBDCEFFTFY-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50629592   

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Henan University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50629592(CHEMBL5415967)
Affinity DataIC50: 8.40nMAssay Description:Inhibition of human FLT3 using EAIYAAPFAKKK and [gamma-33P]-ATP as substrate pretreated for 20 mins followed by [gamma-33P]-ATP addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2024
Entry Details
PubMed
TargetCyclin-dependent kinase 6(Human)
Henan University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50629592(CHEMBL5415967)
Affinity DataIC50: 125nMAssay Description:Inhibition of human CDK6 pretreated for 20 mins followed by [gamma-33P]-ATP addition and measured after 120 mins in presence of 10 uM ATP by radiomet...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2024
Entry Details
PubMed
TargetCyclin-dependent kinase 2(Human)
Henan University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50629592(CHEMBL5415967)
Affinity DataIC50: 193nMAssay Description:Inhibition of human CDK2 pretreated for 20 mins followed by [gamma-33P]-ATP addition and measured after 120 mins in presence of 10 uM ATP by radiomet...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2024
Entry Details
PubMed