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Compound Detail

CHEMBL4862755

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O=C(NC[C@@H]1[C@H]2C[C@H](n3cnc4cc(F)c(F)cc43)C[C@@H]12)c1ccc(Cl)cc1

Basic Information

ChEMBL ID CHEMBL4862755
Phase Preclinical
Structure Type MOL
InChI Key AYCFYWXCYNLGIN-RUPPMWDTSA-N
3
Targets
3
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

401.8
MW (Da)
4.60
ALogP
3
HBA
1
HBD
46.9
PSA (Ų)
0.69
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H18ClF2N3O
MW 401.84
Aromatic Rings 3
Heavy Atoms 28
NP-Likeness -0.94

Activity Summary

IC50 3 meas. best 7.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
IC50 7.72 7.72 19.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.32 5.32 4800.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 5.21 5.21 6200.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 100.0 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