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Compound Detail

CHEMBL2022388

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CC1(C)[C@@H](O)CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@@](C)(C(=O)OCc6ccc([N+](=O)[O-])cc6)CC[C@]5(C)CC[C@@]4(C)[C@]3(C)CC[C@@H]12

Basic Information

ChEMBL ID CHEMBL2022388
Phase Preclinical
Structure Type MOL
InChI Key WVIQQAVOJYUOOE-CJBAOGIUSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

605.8
MW (Da)
7.98
ALogP
6
HBA
1
HBD
106.7
PSA (Ų)
0.21
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H51NO6
MW 605.82
Aromatic Rings 1
Heavy Atoms 44
NP-Likeness 2.07

Activity Summary

IC50 2 meas. best 5.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatitis B virus
CHEMBL613497
IC50 5.05 5.05 8900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Hepatitis B virus IC50 = 8900.0 nM 5.05 Antiviral activity against Hepatitis B virus infected in human HepG2(2.2.15) cel... 22520261

Literature References

PubMed DOI Target Context # Activities
22520261 10.1016/j.bmcl.2012.03.081 Hepatitis B virus 3
22520261 10.1016/j.bmcl.2012.03.081 Unchecked 3
22520261 10.1016/j.bmcl.2012.03.081 ADMET 1

Data from ChEMBL 36 via Core Engine