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Compound Detail

CHEMBL474539

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C=C(C)[C@@H]1CC[C@]2(C)[C@H](C(=O)C=C3[C@@H]4C[C@@](C)(C(=O)Nc5ccccc5)CC[C@]4(C)CC[C@]32C)[C@@]1(C)CCC(=O)OC

Basic Information

ChEMBL ID CHEMBL474539
Phase Preclinical
Structure Type MOL
InChI Key JQCNTBJCNYAOBZ-QGWSXVNMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

573.8
MW (Da)
8.32
ALogP
4
HBA
1
HBD
72.5
PSA (Ų)
0.27
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H51NO4
MW 573.82
Aromatic Rings 1
Heavy Atoms 42
NP-Likeness 1.90

Activity Summary

IC50 1 meas. best 4.81

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
RAW264.7
CHEMBL612557
IC50 4.81 4.81 15500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
RAW264.7 IC50 = 15500.0 nM 4.81 Inhibition of LPS-induced TNFalpha release in mouse RAW264.7 cells pretreated 1 ... 19278854

Literature References

PubMed DOI Target Context # Activities
19278854 10.1016/j.bmc.2009.02.025 RAW264.7 2

Data from ChEMBL 36 via Core Engine