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Compound Detail

CHEMBL3605606

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CC(C)C(=O)Nc1ccc(N(C(=O)Cn2cnc3ccccc32)C(C(=O)NC(C)(C)C)c2ccsc2)cc1

Basic Information

ChEMBL ID CHEMBL3605606
Phase Preclinical
Structure Type MOL
InChI Key BROWYSAZDJJFMS-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

531.7
MW (Da)
5.38
ALogP
6
HBA
2
HBD
96.3
PSA (Ų)
0.32
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H33N5O3S
MW 531.68
Aromatic Rings 4
Heavy Atoms 38
NP-Likeness -2.06

Activity Summary

IC50 1 meas. best 4.28

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.28 4.28 52300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 52300.0 nM 4.28 Inhibition of Tylonycteris bat coronavirus HKU4 N-terminal His6-tagged 3CLpro ex... 26190463

Literature References

PubMed DOI Target Context # Activities
26190463 10.1016/j.bmc.2015.06.039 Unchecked 3

Data from ChEMBL 36 via Core Engine