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Compound Detail

CHEMBL5425798

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CC(C)(O)c1cnc(OCc2cn(-c3ccc(F)c(OC(F)F)c3)nn2)nc1

Basic Information

ChEMBL ID CHEMBL5425798
Phase Preclinical
Structure Type MOL
InChI Key HTKDZSSUNSIGLN-UHFFFAOYSA-N
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

395.3
MW (Da)
2.60
ALogP
8
HBA
1
HBD
95.2
PSA (Ų)
0.66
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H16F3N5O3
MW 395.34
Aromatic Rings 3
Heavy Atoms 28
NP-Likeness -1.93

Activity Summary

IC50 3 meas. best 7.31
Ki 1 meas. best 7.24

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Glutamate NMDA receptor; GRIN1/GRIN2B
CHEMBL1907603
IC50 7.31 7.24 49.0 2
Glutamate receptor ionotropic, NMDA 2B
CHEMBL311
Ki 7.24 7.24 57.0 1
Retinoic acid receptor RXR-alpha
CHEMBL2061
IC50 7.17 7.17 68.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
36757100 10.1021/acs.jmedchem.2c01916 No relevant target 2
36757100 10.1021/acs.jmedchem.2c01916 Glutamate NMDA receptor; GRIN1/GRIN2B 1
36757100 10.1021/acs.jmedchem.2c01916 Glutamate receptor ionotropic, NMDA 2B 1
36757100 10.1021/acs.jmedchem.2c01916 Voltage-gated inwardly rectifying potassium channel KCNH2 1
36757100 10.1021/acs.jmedchem.2c01916 ADMET 1

Data from ChEMBL 36 via Core Engine