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Compound Detail

CHEMBL4205416

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COc1ccc(NC(=O)N2CCN(c3nc(N)nc4sc(-c5cccnc5)nc34)CC2)cc1

Basic Information

ChEMBL ID CHEMBL4205416
Phase Preclinical
Structure Type MOL
InChI Key RTWZCNGWNJMPBW-UHFFFAOYSA-N
3
Targets
4
Activities
1
Assay Types
2
PK Parameters
5
Publications
0
Known Names

Molecular Properties

462.5
MW (Da)
3.09
ALogP
9
HBA
2
HBD
122.4
PSA (Ų)
0.47
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 C22H22N8O2S
MW 462.54
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.74

Activity Summary

IC50 4 meas. best 8.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Phosphatidylinositol 4-kinase beta
CHEMBL3268
IC50 8.7 8.55 2.0 2
Cytochrome P450 3A4
CHEMBL340
IC50 5.8 5.8 1600.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.66 5.66 2200.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 35.0 mL.min-1.g-1 Homo sapiens
CL 87.0 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