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Compound Detail

CHEMBL4286054

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CC(=O)O[C@@H]1CC[C@@]2(C)[C@@H]3CC[C@](C)(O)CC=C3CC[C@@H]2C1(C)C

Basic Information

ChEMBL ID CHEMBL4286054
Phase Preclinical
Structure Type MOL
InChI Key KYIGPMJFJONPDG-VLFNSIGCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

334.5
MW (Da)
4.63
ALogP
3
HBA
1
HBD
46.5
PSA (Ų)
0.56
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H34O3
MW 334.50
Aromatic Rings 0
Heavy Atoms 24
NP-Likeness 3.32

Activity Summary

IC50 1 meas. best 5.24

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
IC50 5.24 5.24 5735.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X IC50 = 5735.0 nM 5.24 Inhibition of human coagulation factor 10a using Z-D-Arg-Gly-Arg-pNA.2HCl as sub... 30340898

Literature References

PubMed DOI Target Context # Activities
30340898 10.1016/j.bmcl.2018.05.036 Coagulation factor X 1

Data from ChEMBL 36 via Core Engine