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Compound Detail

CHEMBL521531

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CCOC(=O)N[C@@H]1CC[C@@H]2[C@@H](C1)C[C@H]1C(=O)O[C@H](C)[C@H]1[C@H]2/C=C/c1ccc(-c2cccc(Cl)c2)cn1

Basic Information

ChEMBL ID CHEMBL521531
Phase Preclinical
Structure Type MOL
InChI Key GNMMTCANYLSJCJ-QHNZEKIYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

509.1
MW (Da)
6.14
ALogP
5
HBA
1
HBD
77.5
PSA (Ų)
0.49
QED
2
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H33ClN2O4
MW 509.05
Aromatic Rings 2
Heavy Atoms 36
NP-Likeness -0.03

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

Data from ChEMBL 36 via Core Engine