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Compound Detail

CHEMBL4461858

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COC(=O)[C@H]1CC[C@H]([C@H](O)CC2c3ccccc3-c3cncn32)CC1

Basic Information

ChEMBL ID CHEMBL4461858
Phase Preclinical
Structure Type MOL
InChI Key PJZVULFUQSLZMW-KJHHTXRZSA-N
1
Targets
2
Activities
2
Assay Types
1
PK Parameters
7
Publications
0
Known Names

Molecular Properties

340.4
MW (Da)
3.18
ALogP
5
HBA
1
HBD
64.3
PSA (Ų)
0.87
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 C20H24N2O3
MW 340.42
Aromatic Rings 2
Heavy Atoms 25
NP-Likeness 0.12

Activity Summary

EC50 1 meas. best 6.66
IC50 1 meas. best 6.55

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
EC50 6.66 6.66 220.0 1
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
IC50 6.55 6.55 280.0 1

Pharmacokinetic Data

Parameter Value Units Species
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