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Compound Detail

CHEMBL1911139

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C=C1C(=O)O[C@H]2C=C(C)[C@H]3CC[C@@](C)(O)[C@@H]3[C@@H](OC(C)=O)[C@H]12

Basic Information

ChEMBL ID CHEMBL1911139
Phase Preclinical
Structure Type MOL
InChI Key PLSCGWSBZMOKAA-RURKYGKJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

306.4
MW (Da)
1.75
ALogP
5
HBA
1
HBD
72.8
PSA (Ų)
0.45
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C17H22O5
MW 306.36
Aromatic Rings 0
Heavy Atoms 22
NP-Likeness 3.32

Activity Summary

IC50 1 meas. best 4.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
RAW264.7
CHEMBL612557
IC50 4.77 4.77 17100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
RAW264.7 IC50 = 17100.0 nM 4.77 Antiinflammatory action in mouse RAW264.7 cells assessed as inhibition of LPS-in... 21894898

Literature References

PubMed DOI Target Context # Activities
21894898 10.1021/np200319x RAW264.7 2

Data from ChEMBL 36 via Core Engine