Compound Detail

CHEMBL475820

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Cc1ccc(NC(=O)c2ccc(C(=O)Nc3ccccc3N)cc2)cc1Nc1ncc(-c2cccnc2)cn1

ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID	CHEMBL475820
Phase	Preclinical
Structure Type	MOL
InChI Key	JUZVLELTCCUPPD-UHFFFAOYSA-N

Targets

Activities

Assay Types

PK Parameters

Publications

Known Names

515.6

MW (Da)

5.68

ALogP

HBA

HBD

134.9

PSA (Å²)

0.20

QED

Ro5 Violations

Rot. Bonds

First in Class Prodrug

IC50 10 meas. best 8.15

EC50 1 meas. best 5.98

Target	Type	Best pChEMBL	Mean pChEMBL	Best (nM)	# Data
EOL1 CHEMBL614489	IC50	8.15	8.15	7.0	1
Histone deacetylase 1 CHEMBL325	IC50	6.57	6.57	270.0	1
K562 CHEMBL385	IC50	6.12	6.12	760.0	1
Histone deacetylase CHEMBL2093865	EC50	5.98	5.98	1040.0	1
HeLa CHEMBL399	IC50	5.71	5.71	1970.0	1
CCRF-CEM CHEMBL382	IC50	5.7	5.7	2000.0	1
Platelet-derived growth factor receptor beta CHEMBL1913	IC50	5.58	5.58	2600.0	1
A549 CHEMBL392	IC50	5.45	5.45	3570.0	1
Tyrosine-protein kinase ABL1 CHEMBL1862	IC50	5.39	5.335	4100.0	2
Vascular endothelial growth factor receptor 2 CHEMBL279	IC50	5.01	5.01	9800.0	1

Top measurements by pChEMBL value

Target	Type	Rel.	Value	Units	pChEMBL	Assay	PubMed
EOL1	IC50	=	7.0	nM	8.15	Cytotoxicity against human EOL-1 cells after 72 hrs by alamar-blue cell viabilit...	19301902
Histone deacetylase 1	IC50	=	270.0	nM	6.57	Inhibition of human recombinant HDAC1 expressed in HEK293 cells	19301902
K562	IC50	=	760.0	nM	6.12	Cytotoxicity against human K562 cells after 72 hrs by alamar-blue cell viability...	19301902
Histone deacetylase	EC50	=	1040.0	nM	5.98	Inhibition of HDAC in human HeLa cells assessed as induction of cellular histone...	19301902
HeLa	IC50	=	1970.0	nM	5.71	Cytotoxicity against human HeLa cells after 72 hrs by alamar-blue cell viability...	19301902
CCRF-CEM	IC50	=	2000.0	nM	5.7	Cytotoxicity against human CCRF-CEM cells after 72 hrs by alamar-blue cell viabi...	19301902
Platelet-derived growth factor receptor beta	IC50	=	2600.0	nM	5.58	Inhibition of PDGFRbeta by liquid scintillation counting	19301902
A549	IC50	=	3570.0	nM	5.45	Cytotoxicity against human A549 cells after 72 hrs by alamar-blue cell viability...	19301902
Tyrosine-protein kinase ABL1	IC50	=	4100.0	nM	5.39	Inhibition of c-Abl T315I mutant by liquid scintillation counting	19301902
Tyrosine-protein kinase ABL1	IC50	=	5300.0	nM	5.28	Inhibition of wild-type c-Abl by liquid scintillation counting	19301902
Vascular endothelial growth factor receptor 2	IC50	=	9800.0	nM	5.01	Inhibition of VEGFR2 by liquid scintillation counting	19301902

PubMed	DOI	Target Context	# Activities
19301902	10.1021/jm800988r	Platelet-derived growth factor receptor beta	3
19301902	10.1021/jm800988r	Tyrosine-protein kinase ABL1	2
19301902	10.1021/jm800988r	Bcr/Abl fusion protein	2
19301902	10.1021/jm800988r	Histone deacetylase 1	1
19301902	10.1021/jm800988r	K562	1
19301902	10.1021/jm800988r	Histone deacetylase	1
19301902	10.1021/jm800988r	HeLa	1
19301902	10.1021/jm800988r	Histone deacetylase 6	1
19301902	10.1021/jm800988r	Vascular endothelial growth factor receptor 2	1
19301902	10.1021/jm800988r	Unchecked	1
19301902	10.1021/jm800988r	A549	1
19301902	10.1021/jm800988r	EOL1	1
19301902	10.1021/jm800988r	CCRF-CEM	1

Data from ChEMBL 36 via Core Engine