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

CHEMBL3400477

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
CN(c1ccc2c(c1)CCC2)c1nc(=O)c2cccnc2s1

Basic Information

ChEMBL ID CHEMBL3400477
Phase Preclinical
Structure Type MOL
InChI Key XNHGKRRSOUIEAT-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

309.4
MW (Da)
3.31
ALogP
5
HBA
0
HBD
46.1
PSA (Ų)
0.73
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H15N3OS
MW 309.39
Aromatic Rings 3
Heavy Atoms 22
NP-Likeness -1.29

Activity Summary

IC50 1 meas. best 5.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Neuron
CHEMBL613705
IC50 5.89 5.89 1300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Neuron IC50 = 1300.0 nM 5.89 Inhibition of kainate-induced neurotoxicity in primary rat hippocampal neurons a... 25792143

Literature References

PubMed DOI Target Context # Activities
25792143 10.1016/j.bmc.2015.02.033 Neuron 1

Data from ChEMBL 36 via Core Engine