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Compound Detail

CHEMBL1910839

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CC1(C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(CO)[C@@H]5[C@H](O)C[C@]43C)[C@@H]2C1

Basic Information

ChEMBL ID CHEMBL1910839
Phase Preclinical
Structure Type MOL
InChI Key XRRLUGUSXUFEDF-NJMQRACMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

488.7
MW (Da)
5.18
ALogP
4
HBA
4
HBD
98.0
PSA (Ų)
0.40
QED
1
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C30H48O5
MW 488.71
Aromatic Rings 0
Heavy Atoms 35
NP-Likeness 3.38

Activity Summary

IC50 1 meas. best 5.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.85 5.85 1400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1400.0 nM 5.85 Inhibition of TNF-alpha-induced NFkappaB activation in human HepG2 cells after 1... 21870831

Literature References

PubMed DOI Target Context # Activities
21870831 10.1021/np200382s Unchecked 3
31429278 10.1021/acs.jnatprod.9b00463 Haemophilus influenzae 3
21870831 10.1021/np200382s HepG2 1

Data from ChEMBL 36 via Core Engine