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Compound Detail

CHEMBL4450473

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O=C(N[C@H]1CC[C@H](C(O)CC2c3ccccc3-c3cncn32)CC1)c1ccccc1

Basic Information

ChEMBL ID CHEMBL4450473
Phase Preclinical
Structure Type MOL
InChI Key GGPLEOHHSWNDKN-HHVDKCBWSA-N
5
Targets
6
Activities
2
Assay Types
1
PK Parameters
8
Publications
0
Known Names

Molecular Properties

401.5
MW (Da)
4.19
ALogP
4
HBA
2
HBD
67.2
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 C25H27N3O2
MW 401.51
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.27

Activity Summary

IC50 4 meas. best 7.3
EC50 2 meas. best 7.07

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
IC50 7.3 7.3 50.0 1
Indoleamine 2,3-dioxygenase 1
CHEMBL4685
EC50 7.07 7.07 86.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.92 5.92 1200.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.17 5.17 6800.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
EC50 4.52 4.52 30000.0 1
Cytochrome P450 2B6
CHEMBL4729
IC50 4.09 4.09 82000.0 1

Pharmacokinetic Data

Parameter Value Units Species
Fu 0.027 - Not specified

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
31264862 10.1021/acs.jmedchem.9b00662 No relevant target 3
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