Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL3739648

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
Cc1ccc(-c2ccnn(C)c2=O)cc1NC(=O)C1=CN(C)C(=O)C[C@H]1c1ccc(F)cc1

Basic Information

ChEMBL ID CHEMBL3739648
Phase Preclinical
Structure Type MOL
InChI Key YGBPQQRANAKAKZ-FQEVSTJZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

446.5
MW (Da)
3.36
ALogP
5
HBA
1
HBD
84.3
PSA (Ų)
0.67
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H23FN4O3
MW 446.48
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -1.04

Activity Summary

IC50 1 meas. best 8.22

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2X purinoceptor 7
CHEMBL4805
IC50 8.22 8.22 6.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
P2X purinoceptor 7 IC50 = 6.0 nM 8.22 Antagonist activity at P2X7R in human whole blood assessed as inhibition of LPS-... 26460788

Literature References

PubMed DOI Target Context # Activities
26460788 10.1021/acs.jmedchem.5b00365 P2X purinoceptor 7 1
26460788 10.1021/acs.jmedchem.5b00365 Salmonella typhimurium 1

Data from ChEMBL 36 via Core Engine