Compound Detail

CHEMBL510179

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CC[C@H](CO)Nc1nc(NCc2cccc(-c3ccccc3)c2)c2ncn(C(C)C)c2n1

ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID	CHEMBL510179
Phase	Preclinical
Structure Type	MOL
InChI Key	RDFGFXPSQFBJGT-OAQYLSRUSA-N

Targets

Activities

Assay Types

PK Parameters

Publications

Known Names

430.6

MW (Da)

4.87

ALogP

HBA

HBD

87.9

PSA (Å²)

0.35

QED

Ro5 Violations

Rot. Bonds

First in Class Prodrug

IC50 5 meas. best 5.96

Target	Type	Best pChEMBL	Mean pChEMBL	Best (nM)	# Data
Unchecked CHEMBL612545	IC50	5.96	5.68	1100.0	3
SH-SY5Y CHEMBL614910	IC50	5.62	5.62	2400.0	1
HEK293 CHEMBL614818	IC50	5.6	5.6	2500.0	1

Top measurements by pChEMBL value

Target	Type	Rel.	Value	Units	pChEMBL	Assay	PubMed
Unchecked	IC50	=	1100.0	nM	5.96	Inhibition of pig brain CK1	18698753
SH-SY5Y	IC50	=	2400.0	nM	5.62	Antiproliferative activity against human SH-SY5Y cells assessed as survival afte...	18698753
HEK293	IC50	=	2500.0	nM	5.6	Antiproliferative activity against HEK293 cells assessed as survival after 48 hr...	18698753
Unchecked	IC50	=	2600.0	nM	5.58	Inhibition of human recombinant CDK5/p25 by scintillation method	18698753
Unchecked	IC50	=	3200.0	nM	5.5	Inhibition of starfish oocyte CDK1/cyclin B by scintillation method	18698753

PubMed	DOI	Target Context	# Activities
18698753	10.1021/jm800109e	Unchecked	3
18698753	10.1021/jm800109e	Glycogen synthase kinase-3	1
18698753	10.1021/jm800109e	SH-SY5Y	1
18698753	10.1021/jm800109e	HEK293	1

Data from ChEMBL 36 via Core Engine