Compound Detail

CHEMBL5556268

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NC1CCN(C(=O)c2ccc(-c3ccc4ncc(-c5cc6ccccc6o5)n4c3)cc2)CC1

ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID	CHEMBL5556268
Phase	Preclinical
Structure Type	MOL
InChI Key	GXUYZVYTXZYDQM-UHFFFAOYSA-N

Targets

Activities

Assay Types

PK Parameters

Publications

Known Names

436.5

MW (Da)

4.98

ALogP

HBA

HBD

76.8

PSA (Å²)

0.43

QED

Ro5 Violations

Rot. Bonds

Availability	Unknown
Chirality	Unknown

First in Class Prodrug

IC50 11 meas. best 9.22

Target	Type	Best pChEMBL	Mean pChEMBL	Best (nM)	# Data
MAP kinase-interacting serine/threonine-protein kinase 2 CHEMBL4204	IC50	9.22	9.22	0.6	1
MAP kinase-interacting serine/threonine-protein kinase 1 CHEMBL4718	IC50	8.49	8.49	3.2	1
Eukaryotic translation initiation factor 4E CHEMBL4848	IC50	6.84	6.84	146.0	1
DOHH-2 CHEMBL2366181	IC50	5.72	5.72	1900.0	1
HT-29 CHEMBL384	IC50	5.7	5.7	2000.0	1
MDA-MB-231 CHEMBL400	IC50	5.42	5.42	3800.0	1
Voltage-gated inwardly rectifying potassium channel KCNH2 CHEMBL240	IC50	5.36	5.36	4400.0	1
PC-3 CHEMBL390	IC50	5.29	5.29	5100.0	1
TMD8 CHEMBL4296503	IC50	5.26	5.26	5500.0	1
PANC-1 CHEMBL614139	IC50	5.21	5.21	6100.0	1
A549 CHEMBL392	IC50	5.11	5.11	7800.0	1

Parameter	Value	Units	Species
T1/2	2.0	hr	Homo sapiens
T1/2	2.0	hr	Canis lupus familiaris
T1/2	2.0	hr	Rattus norvegicus

Top measurements by pChEMBL value

Target	Type	Rel.	Value	Units	pChEMBL	Assay	PubMed
MAP kinase-interacting serine/threonine-protein kinase 2	IC50	=	0.6	nM	9.22	Inhibition of recombinant MNK2 (unknown origin) using TATKSGSTTKNR as substrate ...	38564512
MAP kinase-interacting serine/threonine-protein kinase 1	IC50	=	3.2	nM	8.49	Inhibition of recombinant MNK1 (unknown origin) using TATKSGSTTKNR as substrate ...	38564512
Eukaryotic translation initiation factor 4E	IC50	=	146.0	nM	6.84	Inhibition of eIF4E phosphorylation at ser209 residue in human HeLa cells incuba...	38564512
DOHH-2	IC50	=	1900.0	nM	5.72	Antiproliferative activity against human DOHH-2 cells assessed as inhibition of ...	38564512
HT-29	IC50	=	2000.0	nM	5.7	Antiproliferative activity against human HT-29 cells assessed as inhibition of c...	38564512
MDA-MB-231	IC50	=	3800.0	nM	5.42	Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition...	38564512
Voltage-gated inwardly rectifying potassium channel KCNH2	IC50	=	4400.0	nM	5.36	Inhibition of hERG expressed in HEK293 cells at -80 mV holding potential by patc...	38564512
PC-3	IC50	=	5100.0	nM	5.29	Antiproliferative activity against human PC-3 cells assessed as inhibition of ce...	38564512
TMD8	IC50	=	5500.0	nM	5.26	Antiproliferative activity against human TMD8 cells assessed as inhibition of ce...	38564512
PANC-1	IC50	=	6100.0	nM	5.21	Antiproliferative activity against human PANC-1 cells assessed as inhibition of ...	38564512
A549	IC50	=	7800.0	nM	5.11	Antiproliferative activity against human A549 cells assessed as inhibition of ce...	38564512

PubMed	DOI	Target Context	# Activities
38564512	10.1021/acs.jmedchem.3c02008	ADMET	3
38564512	10.1021/acs.jmedchem.3c02008	MAP kinase-interacting serine/threonine-protein kinase 1	1
38564512	10.1021/acs.jmedchem.3c02008	MAP kinase-interacting serine/threonine-protein kinase 2	1
38564512	10.1021/acs.jmedchem.3c02008	Eukaryotic translation initiation factor 4E	1
38564512	10.1021/acs.jmedchem.3c02008	TMD8	1
38564512	10.1021/acs.jmedchem.3c02008	DOHH-2	1
38564512	10.1021/acs.jmedchem.3c02008	HT-29	1
38564512	10.1021/acs.jmedchem.3c02008	PC-3	1
38564512	10.1021/acs.jmedchem.3c02008	A549	1
38564512	10.1021/acs.jmedchem.3c02008	PANC-1	1
38564512	10.1021/acs.jmedchem.3c02008	MDA-MB-231	1
38564512	10.1021/acs.jmedchem.3c02008	Voltage-gated inwardly rectifying potassium channel KCNH2	1

Data from ChEMBL 36 via Core Engine