Compound Detail

CHEMBL1242377

Enter ChEMBL ID:

Free Research Context This compound will appear in recent viewed items on the research home for this browser.

CC(C)n1nc(-c2ccc(F)c(O)c2)c2c(N)ncnc21

ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID	CHEMBL1242377
Phase	Preclinical
Structure Type	MOL
InChI Key	CJMMCIXRPVLDBH-UHFFFAOYSA-N

Targets

Activities

Assay Types

PK Parameters

Publications

Known Names

Molecular Properties

287.3

MW (Da)

2.50

ALogP

HBA

HBD

89.8

PSA (Å²)

0.76

QED

Ro5 Violations

Rot. Bonds

Drug Information

Molecule Type	Small molecule
Availability	Unknown
Chirality	Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula	C14H14FN5O
MW	287.30
Aromatic Rings	3
Heavy Atoms	21
NP-Likeness	-0.95

Activity Summary

IC50 14 meas. best 8.16

Target Activity Profile

Target	Type	Best pChEMBL	Mean pChEMBL	Best (nM)	# Data
Proto-oncogene tyrosine-protein kinase Src CHEMBL267	IC50	8.16	8.16	6.9	1
Tyrosine-protein kinase HCK CHEMBL3234	IC50	8.04	8.04	9.2	1
Tyrosine-protein kinase ABL1 CHEMBL1862	IC50	7.85	7.85	14.0	1
Serine/threonine-protein kinase mTOR CHEMBL2842	IC50	7.43	7.43	37.0	1
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform CHEMBL3130	IC50	7.19	7.19	65.0	1
Vascular endothelial growth factor receptor 2 CHEMBL279	IC50	7.17	7.17	68.0	1
DNA-dependent protein kinase catalytic subunit CHEMBL3142	IC50	7.06	7.06	88.0	1
Ephrin type-B receptor 4 CHEMBL5147	IC50	6.78	6.78	166.0	1
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform CHEMBL4005	IC50	6.73	6.73	187.0	1
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform CHEMBL3267	IC50	6.68	6.68	209.0	1
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform CHEMBL3145	IC50	6.21	6.21	613.0	1
Unchecked CHEMBL612545	IC50	6.06	6.06	865.0	1
Epidermal growth factor receptor CHEMBL203	IC50	5.85	5.85	1400.0	1
Phosphatidylinositol 4-kinase beta CHEMBL3268	IC50	5.6	5.6	2500.0	1

Activity Data Samples

Top measurements by pChEMBL value

Target	Type	Rel.	Value	Units	pChEMBL	Assay	PubMed
Proto-oncogene tyrosine-protein kinase Src	IC50	=	6.9	nM	8.16	Inhibition of recombinant c-Src by radioactive phosphotransfer assay in presence...	18849971
Tyrosine-protein kinase HCK	IC50	=	9.2	nM	8.04	Inhibition of recombinant HCK by radioactive phosphotransfer assay in presence o...	18849971
Tyrosine-protein kinase ABL1	IC50	=	14.0	nM	7.85	Inhibition of recombinant c-Abl by radioactive phosphotransfer assay in presence...	18849971
Serine/threonine-protein kinase mTOR	IC50	=	37.0	nM	7.43	Inhibition of recombinant mTOR by radioactive phosphotransfer assay in presence ...	18849971
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform	IC50	=	65.0	nM	7.19	Inhibition of recombinant PI3Kdelta by radioactive phosphotransfer assay in pres...	18849971
Vascular endothelial growth factor receptor 2	IC50	=	68.0	nM	7.17	Inhibition of recombinant VEGFR2 by radioactive phosphotransfer assay in presenc...	18849971
DNA-dependent protein kinase catalytic subunit	IC50	=	88.0	nM	7.06	Inhibition of DNA-PK by radioactive phosphotransfer assay in presence of 10 uM A...	18849971
Ephrin type-B receptor 4	IC50	=	166.0	nM	6.78	Inhibition of recombinant EphB4R by radioactive phosphotransfer assay in presenc...	18849971
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform	IC50	=	187.0	nM	6.73	Inhibition of recombinant PI3Kalpha by radioactive phosphotransfer assay in pres...	18849971
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform	IC50	=	209.0	nM	6.68	Inhibition of recombinant PI3Kgamma by radioactive phosphotransfer assay in pres...	18849971
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform	IC50	=	613.0	nM	6.21	Inhibition of recombinant PI3Kbeta by radioactive phosphotransfer assay in prese...	18849971
Unchecked	IC50	=	865.0	nM	6.06	Inhibition of recombinant c-Src T338I mutant by radioactive phosphotransfer assa...	18849971
Epidermal growth factor receptor	IC50	=	1400.0	nM	5.85	Inhibition of recombinant EGFR by radioactive phosphotransfer assay in presence ...	18849971
Phosphatidylinositol 4-kinase beta	IC50	=	2500.0	nM	5.6	Inhibition of recombinant PI4Kbeta by radioactive phosphotransfer assay in prese...	18849971

Literature References

PubMed	DOI	Target Context	# Activities
18849971	10.1038/nchembio.117	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform	1
18849971	10.1038/nchembio.117	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform	1
18849971	10.1038/nchembio.117	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform	1
18849971	10.1038/nchembio.117	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform	1
18849971	10.1038/nchembio.117	Serine/threonine-protein kinase mTOR	1
18849971	10.1038/nchembio.117	DNA-dependent protein kinase catalytic subunit	1
18849971	10.1038/nchembio.117	Phosphatidylinositol 4-kinase beta	1
18849971	10.1038/nchembio.117	Tyrosine-protein kinase ABL1	1
18849971	10.1038/nchembio.117	Tyrosine-protein kinase HCK	1
18849971	10.1038/nchembio.117	Proto-oncogene tyrosine-protein kinase Src	1
18849971	10.1038/nchembio.117	Unchecked	1
18849971	10.1038/nchembio.117	Vascular endothelial growth factor receptor 2	1
18849971	10.1038/nchembio.117	Epidermal growth factor receptor	1
18849971	10.1038/nchembio.117	Ephrin type-B receptor 4	1

Data from ChEMBL 36 via Core Engine