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

CHEMBL493975

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
C[C@H]1OC(=O)[C@@H]2C[C@@H]3C[C@H](NS(C)(=O)=O)CC[C@H]3[C@H](/C=C/c3ccc(-c4cccc(F)c4)cn3)[C@H]12

Basic Information

ChEMBL ID CHEMBL493975
Phase Preclinical
Structure Type MOL
InChI Key CKKWHHWNHZSSPN-LIWLXMMZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

498.6
MW (Da)
4.43
ALogP
5
HBA
1
HBD
85.4
PSA (Ų)
0.62
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H31FN2O4S
MW 498.62
Aromatic Rings 2
Heavy Atoms 35
NP-Likeness -0.15

Activity Summary

Ki 1 meas. best 7.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Proteinase-activated receptor 1
CHEMBL3974
Ki 7.96 7.96 11.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Proteinase-activated receptor 1 Ki = 11.0 nM 7.96 Displacement of [3H]haTRAP from PAR1 in human platelets 18447380

Literature References

PubMed DOI Target Context # Activities
18447380 10.1021/jm800180e Proteinase-activated receptor 1 1
18447380 10.1021/jm800180e Platelet 1

Data from ChEMBL 36 via Core Engine