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Compound Detail

CHEMBL3426598

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COc1ccc(-c2c(C)nc3c(NCCN4CCOCC4)ccnn23)cc1OC

Basic Information

ChEMBL ID CHEMBL3426598
Phase Preclinical
Structure Type MOL
InChI Key CFLABOGUXKYRSK-UHFFFAOYSA-N
4
Targets
6
Activities
2
Assay Types
0
PK Parameters
10
Publications
0
Known Names

Molecular Properties

397.5
MW (Da)
2.47
ALogP
8
HBA
1
HBD
73.2
PSA (Ų)
0.66
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H27N5O3
MW 397.48
Aromatic Rings 3
Heavy Atoms 29
NP-Likeness -1.47

Activity Summary

EC50 4 meas. best 6.43
IC50 2 meas. best 7.03

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 7.03 5.795 93.0 2
Hepatitis C virus
CHEMBL379
EC50 6.43 5.59 370.0 2
Coxsackievirus B3
CHEMBL613554
EC50 6.3 6.3 500.0 1
Human rhinovirus sp.
CHEMBL612470
EC50 6.06 6.06 880.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
25897704 10.1021/acs.jmedchem.5b00499 Unchecked 2
25897704 10.1021/acs.jmedchem.5b00499 Hepatitis C virus 2
25897704 10.1021/acs.jmedchem.5b00499 Human rhinovirus sp. 1
25897704 10.1021/acs.jmedchem.5b00499 Coxsackievirus B3 1
25897704 10.1021/acs.jmedchem.5b00499 Phosphatidylinositol 4-kinase type 2-alpha 1
25897704 10.1021/acs.jmedchem.5b00499 HeLa 1
25897704 10.1021/acs.jmedchem.5b00499 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform 1
25897704 10.1021/acs.jmedchem.5b00499 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform 1
25897704 10.1021/acs.jmedchem.5b00499 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform 1
25897704 10.1021/acs.jmedchem.5b00499 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform 1

Data from ChEMBL 36 via Core Engine