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

CHEMBL3893989

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=C1CCC[C@H]2[C@](C)(Cc3cc(OC)ccc3O)[C@@H](C)CC[C@]12C

Basic Information

ChEMBL ID CHEMBL3893989
Phase Preclinical
Structure Type MOL
InChI Key IBICYDHHUHLVJM-JJCGOBCMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

328.5
MW (Da)
5.74
ALogP
2
HBA
1
HBD
29.5
PSA (Ų)
0.72
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C22H32O2
MW 328.50
Aromatic Rings 1
Heavy Atoms 24
NP-Likeness 2.46

Activity Summary

IC50 1 meas. best 4.98

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.98 4.98 10400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 10400.0 nM 4.98 Inhibition of SOAT-mediated oleic acid-induced [14C]cholesterol ester accumulati... 31253530

Literature References

PubMed DOI Target Context # Activities
31253530 10.1016/j.bmcl.2019.06.026 Unchecked 2
27336796 10.1021/acs.jnatprod.6b00367 Tyrosine-protein phosphatase non-receptor type 1 1
31253530 10.1016/j.bmcl.2019.06.026 CHO-K1 1

Data from ChEMBL 36 via Core Engine