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Compound Detail

CHEMBL1910835

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CC1(C)CC[C@]2(C(=O)O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)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 CHEMBL1910835
Phase Preclinical
Structure Type MOL
InChI Key ACQGRYACYVKOBB-ONXNPAKPSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

650.9
MW (Da)
2.44
ALogP
10
HBA
7
HBD
177.1
PSA (Ų)
0.18
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C36H58O10
MW 650.85
Aromatic Rings 0
Heavy Atoms 46
NP-Likeness 3.10

Activity Summary

IC50 1 meas. best 4.79

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.79 4.79 16400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 16400.0 nM 4.79 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
21870831 10.1021/np200382s HepG2 1

Data from ChEMBL 36 via Core Engine