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Compound Detail

CHEMBL4576829

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OC(CC1c2c(F)cccc2-c2cncn21)C1CCC(F)(F)CC1

Basic Information

ChEMBL ID CHEMBL4576829
Phase Preclinical
Structure Type MOL
InChI Key FPKRCRNJVIHTNG-UHFFFAOYSA-N
3
Targets
4
Activities
2
Assay Types
2
PK Parameters
7
Publications
0
Known Names

Molecular Properties

336.4
MW (Da)
4.17
ALogP
3
HBA
1
HBD
38.0
PSA (Ų)
0.91
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C18H19F3N2O
MW 336.36
Aromatic Rings 2
Heavy Atoms 24
NP-Likeness -0.02

Activity Summary

IC50 3 meas. best 7.0
EC50 1 meas. best 7.03

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
EC50 7.03 7.03 93.0 1
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
IC50 7.0 7.0 100.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.58 5.58 2600.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 4.7 4.7 20000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 15.27 mL.min-1.kg-1 Homo sapiens
Fu - - Not specified

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
31264862 10.1021/acs.jmedchem.9b00662 Indoleamine 2,3-dioxygenase 1 2
31264862 10.1021/acs.jmedchem.9b00662 ADMET 2
31264862 10.1021/acs.jmedchem.9b00662 Cytochrome P450 3A4 1
31264862 10.1021/acs.jmedchem.9b00662 Cytochrome P450 2D6 1
31264862 10.1021/acs.jmedchem.9b00662 Cytochrome P450 1A2 1
31264862 10.1021/acs.jmedchem.9b00662 Cytochrome P450 2B6 1
31264862 10.1021/acs.jmedchem.9b00662 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine