BDBM720664 (R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2,3-c]pyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine ::US20250051362, Compound 19::US12435095, Compound 19

SMILES C[C@@H]1COCCN1c1nc(-c2cncc3[nH]ccc23)nc2c1ccn2S(C)(=O)=O

InChI Key InChIKey=USZDDOBUMPPACY-UHFFFAOYSA-N

  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 18 hits for monomerid = 720664   

TargetSerine/threonine-protein kinase ATR(Human)
Shanghai Annova Biotechnology

US Patent
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.60nMAssay Description:The inhibitory activity of the compounds on ATR kinase in vitro was determined by Mobility Shift Assay at an ATP concentration of Km using Caliper EZ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/17/2025
Entry Details
US Patent

LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.60nMAssay Description:Inhibition of ATR/ATRIP (unknown origin) using 5-FAM-AK-17 as substrate preincubated with compound for 10 mins followed by ATP addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
TargetSerine/threonine-protein kinase ATR(Human)
Shanghai Annova Biotechnology

US Patent
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.60nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
US Patent

LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 22nMAssay Description:Inhibition of human mTORMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 4.95E+3nMAssay Description:Inhibition of human LCKMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human JAK1More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
TargetAurora kinase B(Human)TBA
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human Aurora BMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AMPK alpha2/beta1/gamma1More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human CDK2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human DRAK2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human LYNMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human FLT3More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ARK5More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human BTKMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ABLMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human MERMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human IRAK4More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed
LigandPNGBDBM720664((R)-3-methyl-4-(7-(methylsulfonyl)-2-(1H-pyrrolo[2...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human BRSK2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
TBA
Entry Details
PubMed