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Compound Detail

CHEMBL329164

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CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)O[C@H](C)[C@@H](C)[C@H]3OC

Basic Information

ChEMBL ID CHEMBL329164
Phase Preclinical
Structure Type MOL
InChI Key KEWWSURXGADRPV-VLXJIEOASA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

384.5
MW (Da)
5.03
ALogP
5
HBA
0
HBD
57.9
PSA (Ų)
0.69
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C23H28O5
MW 384.47
Aromatic Rings 2
Heavy Atoms 28
NP-Likeness 2.24

Activity Summary

IC50 1 meas. best 4.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
CEM-SS
CHEMBL614548
IC50 4.72 4.72 19000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
CEM-SS IC50 = 19000.0 nM 4.72 Concentration inhibiting HIV-1 induced cytopathic effects in human T-lymphoblast... 1379639

Literature References

PubMed DOI Target Context # Activities
1379639 10.1021/jm00093a004 CEM-SS 2

Data from ChEMBL 36 via Core Engine