Compound Detail

CHEMBL557383

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CN(C)Cc1cc(C(=O)/C=C/c2cccc(Cl)c2)cc(CN(C)C)c1O.Cl

ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID	CHEMBL557383
Phase	Preclinical
Structure Type	MOL
InChI Key	PDMSUGVVKLXXIG-HRNDJLQDSA-N
Parent Compound	CHEMBL1196546
Active Moiety	CHEMBL1196546

Targets

Activities

Assay Types

PK Parameters

Publications

Known Names

372.9

MW (Da)

4.06

ALogP

HBA

HBD

43.8

PSA (Å²)

0.59

QED

Ro5 Violations

Rot. Bonds

First in Class Prodrug

IC50 5 meas. best 5.57

Target	Type	Best pChEMBL	Mean pChEMBL	Best (nM)	# Data
Homo sapiens CHEMBL372	IC50	5.57	5.405	2680.0	2
Tumor Cell line CHEMBL613974	IC50	5.33	5.33	4680.0	1
L1210 CHEMBL386	IC50	5.22	5.22	5960.0	1
P388 CHEMBL389	IC50	5.06	5.06	8660.0	1

Top measurements by pChEMBL value

Target	Type	Rel.	Value	Units	pChEMBL	Assay	PubMed
Homo sapiens	IC50	=	2680.0	nM	5.57	Concentration required to inhibit 50% growth of Human CEM T-lymphocytes cells	9544201
Tumor Cell line	IC50	=	4680.0	nM	5.33	Evaluation for cytotoxicity to human tumor cell lines.	9544201
Homo sapiens	IC50	=	5750.0	nM	5.24	Concentration required to inhibit 50% growth of human Molt 4/C8 T-lymphocyte cel...	9544201
L1210	IC50	=	5960.0	nM	5.22	Concentration required to inhibit 50% growth of L1210 leukemia cells	9544201
P388	IC50	=	8660.0	nM	5.06	Inhibition of proliferation of murine P388 cells	9544201

PubMed	DOI	Target Context	# Activities
9544201	10.1021/jm970432t	Homo sapiens	2
9544201	10.1021/jm970432t	P388	1
9544201	10.1021/jm970432t	L1210	1
9544201	10.1021/jm970432t	Tumor Cell line	1

Data from ChEMBL 36 via Core Engine