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Compound Detail

CHEMBL4864365

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O=C(Nc1cncc(Cl)c1)c1cccc2[nH]ccc12

Basic Information

ChEMBL ID CHEMBL4864365
Phase Preclinical
Structure Type MOL
InChI Key SBSRQTRJDPJOIX-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

271.7
MW (Da)
3.47
ALogP
2
HBA
2
HBD
57.8
PSA (Ų)
0.75
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H10ClN3O
MW 271.71
Aromatic Rings 3
Heavy Atoms 19
NP-Likeness -1.66

Activity Summary

IC50 1 meas. best 4.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.0 4.0 100000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 100000.0 nM 4.0 Inhibition of SARS-CoV-2 3CL protease using HiyteFluor-488ESATL-QSGLRKAK-(QXL)-N... 34528437

Literature References

PubMed DOI Target Context # Activities
34528437 10.1021/acs.jmedchem.1c01214 Unchecked 1
34528437 10.1021/acs.jmedchem.1c01214 SARS-CoV-2 1

Data from ChEMBL 36 via Core Engine