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Compound Detail

CHEMBL4853456

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CCC(NC(=O)c1ccc(Cl)cc1)[C@H]1[C@@H]2C[C@@H](n3cnc4ncc(C#N)cc43)C[C@@H]21

Basic Information

ChEMBL ID CHEMBL4853456
Phase Preclinical
Structure Type MOL
InChI Key YCEWCDQCRWLWQD-IAZBLINFSA-N
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

419.9
MW (Da)
4.36
ALogP
5
HBA
1
HBD
83.6
PSA (Ų)
0.67
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H22ClN5O
MW 419.92
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.77

Activity Summary

IC50 2 meas. best 6.45

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
IC50 6.45 6.45 357.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.28 5.28 5200.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 4.5 mL.min-1.kg-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34292726 10.1021/acs.jmedchem.1c00679 ADMET 2
34292726 10.1021/acs.jmedchem.1c00679 Indoleamine 2,3-dioxygenase 1 1
34292726 10.1021/acs.jmedchem.1c00679 Cytochrome P450 2C9 1
34292726 10.1021/acs.jmedchem.1c00679 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine