BDBM591167 2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-pyrido[2,3-b][1,4]oxazin-7- yl)isoquinolin-3-yl)amino)-6-isopropyl- 5,6-dihydro-4H-pyrazolo[1,5- [d][1,4]diazepin-7(8H)-one::US11566003, Compound 233

SMILES CC(C)N1CCc2cc(Nc3cc4cc(c(F)c(N)c4cn3)-c3cnc4OCCNc4c3C)nn2CC1=O

InChI Key InChIKey=JOMBGXFENCGRHG-UHFFFAOYSA-N

Data  1 KI  3 IC50  1 EC50

  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 5 hits for monomerid = 591167   

TargetMitogen-activated protein kinase kinase kinase kinase 1(Human)
Emd Serono Research & Development Institute

Curated by ChEMBL
LigandPNGBDBM591167(2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-p...)
Affinity DataIC50: 18nMAssay Description:Inhibition of human HPK1 in human Jurkat cells assessed as reduction in SLP76 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 1(Human)
Emd Serono Research & Development Institute

Curated by ChEMBL
LigandPNGBDBM591167(2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-p...)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of full-length human GST-tagged HPK1 expressed in baculovirus infected Sf21 insect cells using MBP and ATP as substrate preincubated for 1...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 1(Human)
Emd Serono Research & Development Institute

Curated by ChEMBL
LigandPNGBDBM591167(2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-p...)
Affinity DataIC50: 10nMAssay Description:Inhibition of human HPK1 in human Jurkat cells assessed as reduction in SLP76 phosphorylation at Ser376 residue preincubated for 60 mins followed by ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 1(Human)
Emd Serono Research & Development Institute

Curated by ChEMBL
LigandPNGBDBM591167(2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-p...)
Affinity DataEC50:  12nMAssay Description:Inhibition of human HPK1 in anti-humanCD3/anti-humanCD28 stimulated human CD3-positive T cells assessed as increase in IL-2 release incubated for 48 ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 1(Human)
Emd Serono Research & Development Institute

Curated by ChEMBL
LigandPNGBDBM591167(2-((8-amino-7-fluoro-6-(8-methyl-2,3- dihydro-1H-p...)
Affinity DataKi:  0.0180nMAssay Description:To a 384 well Proxiplate with 80 nL compound or DMSO spotted on was added 4 μl/well kinase mix. The mixture was preincubated for 30 minutes and ...More data for this Ligand-Target Pair
In DepthDetails
US Patent