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Compound Detail

CHEMBL498840

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Cc1nc2c(N[C@H]3c4ccccc4C[C@@H]3O)cc(-n3ccccc3=O)cn2c1C

Basic Information

ChEMBL ID CHEMBL498840
Phase Preclinical
Structure Type MOL
InChI Key YPDJKJWWTFDCSB-UNMCSNQZSA-N
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

386.5
MW (Da)
3.17
ALogP
6
HBA
2
HBD
71.6
PSA (Ų)
0.57
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H22N4O2
MW 386.46
Aromatic Rings 4
Heavy Atoms 29
NP-Likeness -0.77

Activity Summary

IC50 3 meas. best 6.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.4 6.4 398.1 1
Cytochrome P450 3A4
CHEMBL340
IC50 4.21 4.21 62000.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 4.01 4.01 97000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 398.11 nM 6.4 Inhibition of H+/K+ ATPase 19467868
Cytochrome P450 3A4 IC50 = 62000.0 nM 4.21 Inhibition of CYP3A4 using diethoxyfluorescein as substrate 19467868
Cytochrome P450 2C9 IC50 = 97000.0 nM 4.01 Inhibition of CYP2C9 19467868

Literature References

PubMed DOI Target Context # Activities
19467868 10.1016/j.bmcl.2009.04.127 Cytochrome P450 3A4 2
19467868 10.1016/j.bmcl.2009.04.127 Rattus norvegicus 2
19467868 10.1016/j.bmcl.2009.04.127 Cytochrome P450 2C9 1
19467868 10.1016/j.bmcl.2009.04.127 Unchecked 1
19467868 10.1016/j.bmcl.2009.04.127 No relevant target 1

Data from ChEMBL 36 via Core Engine