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Compound Detail

CHEMBL4068628

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CCOC(=O)C1=C(CN2CCOC[C@H]2C(=O)O)NC(c2nccs2)=N[C@@H]1c1ccc(Cl)cc1Cl

Basic Information

ChEMBL ID CHEMBL4068628
Phase Preclinical
Structure Type MOL
InChI Key HYOCBTTZXCDPCE-FUHWJXTLSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

525.4
MW (Da)
3.14
ALogP
9
HBA
2
HBD
113.3
PSA (Ų)
0.53
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H22Cl2N4O5S
MW 525.41
Aromatic Rings 2
Heavy Atoms 34
NP-Likeness -1.12

Activity Summary

EC50 1 meas. best 5.61

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatitis B virus
CHEMBL613497
EC50 5.61 5.61 2432.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Hepatitis B virus EC50 = 2432.0 nM 5.61 Antiviral activity against HBV infected in human HepG2.2.15 replicon cells asses... 29381358

Literature References

PubMed DOI Target Context # Activities
29381358 10.1021/acs.jmedchem.7b01914 Cytochrome P450 3A4 4
29381358 10.1021/acs.jmedchem.7b01914 Voltage-gated inwardly rectifying potassium channel KCNH2 1
29381358 10.1021/acs.jmedchem.7b01914 Hepatitis B virus 1

Data from ChEMBL 36 via Core Engine