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Compound Detail

CHEMBL494941

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C=C1/C(=C\C=C2/CCC[C@]3(C)C(C4(C/C=C/C(O)(C(F)(F)F)C(F)(F)F)CC4)=CC[C@@H]23)C[C@@H](O)C[C@@H]1F

Basic Information

ChEMBL ID CHEMBL494941
Phase Preclinical
Structure Type MOL
InChI Key HGQBMSKVCLWAKS-RCZPXKEVSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

534.6
MW (Da)
7.61
ALogP
2
HBA
2
HBD
40.5
PSA (Ų)
0.28
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 C28H33F7O2
MW 534.56
Aromatic Rings 0
Heavy Atoms 37
NP-Likeness 1.75

Activity Summary

IC50 1 meas. best 10.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
PBMC
CHEMBL613107
IC50 10.19 10.19 0.1 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
PBMC IC50 = 0.065 nM 10.19 Inhibition of LPS-induced TNFalpha production in human PBMC after 24 hrs by ELIS... 19309155

Literature References

PubMed DOI Target Context # Activities
19309155 10.1021/jm801365a PBMC 2

Data from ChEMBL 36 via Core Engine