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Compound Detail

CHEMBL4210308

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COc1ccc(NC(=O)N2CCN(c3nc(N)nc4sc(-c5ccccc5)nc34)CC2)cc1

Basic Information

ChEMBL ID CHEMBL4210308
Phase Preclinical
Structure Type MOL
InChI Key GOCXVAMNAGUMGS-UHFFFAOYSA-N
2
Targets
3
Activities
1
Assay Types
2
PK Parameters
5
Publications
0
Known Names

Molecular Properties

461.6
MW (Da)
3.70
ALogP
8
HBA
2
HBD
109.5
PSA (Ų)
0.48
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H23N7O2S
MW 461.55
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.59

Activity Summary

IC50 3 meas. best 7.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Phosphatidylinositol 4-kinase beta
CHEMBL3268
IC50 7.96 7.73 11.0 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.77 5.77 1700.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 13.0 mL.min-1.g-1 Homo sapiens
CL 20.0 mL.min-1.g-1 Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29952567 10.1021/acs.jmedchem.8b00521 Phosphatidylinositol 4-kinase beta 2
29952567 10.1021/acs.jmedchem.8b00521 ADMET 2
29952567 10.1021/acs.jmedchem.8b00521 No relevant target 2
29952567 10.1021/acs.jmedchem.8b00521 Voltage-gated inwardly rectifying potassium channel KCNH2 1
29952567 10.1021/acs.jmedchem.8b00521 Cytochrome P450 3A4 1

Data from ChEMBL 36 via Core Engine