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

CHEMBL1668040

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
CC(C)(C)OC(=O)NCCN/C=C1\C(=O)CC[C@]2(C)C1=C(O)C(=O)c1cc3c(cc12)C(=O)C=CC3=O

Basic Information

ChEMBL ID CHEMBL1668040
Phase Preclinical
Structure Type MOL
InChI Key CQVVKQDJEXYNBP-RCLIWOIXSA-N
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

492.5
MW (Da)
3.25
ALogP
8
HBA
3
HBD
138.9
PSA (Ų)
0.43
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 C27H28N2O7
MW 492.53
Aromatic Rings 1
Heavy Atoms 36
NP-Likeness 0.78

Activity Summary

IC50 3 meas. best 5.13

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Vero
CHEMBL391
IC50 5.13 5.13 7400.0 1
Phospholipase A2
CHEMBL4807
IC50 4.89 4.89 12800.0 1
Plasmodium falciparum
CHEMBL364
IC50 4.28 4.28 52800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
21256013 10.1016/j.bmcl.2010.12.056 Plasmodium falciparum 2
21256013 10.1016/j.bmcl.2010.12.056 Phospholipase A2 1
21256013 10.1016/j.bmcl.2010.12.056 Unchecked 1
21256013 10.1016/j.bmcl.2010.12.056 Protein farnesyltransferase 1
21256013 10.1016/j.bmcl.2010.12.056 Vero 1

Data from ChEMBL 36 via Core Engine