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Compound Detail

CHEMBL3605598

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CC(C)(C)NC(=O)C(c1cccnc1)N(C(=O)Cc1c[nH]c2ccccc12)c1ccc(OCF)cc1

Basic Information

ChEMBL ID CHEMBL3605598
Phase Preclinical
Structure Type MOL
InChI Key FTQDJPYKJYPQFK-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

488.6
MW (Da)
5.10
ALogP
4
HBA
2
HBD
87.3
PSA (Ų)
0.36
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H29FN4O3
MW 488.56
Aromatic Rings 4
Heavy Atoms 36
NP-Likeness -1.32

Activity Summary

IC50 1 meas. best 5.41

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.41 5.41 3900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 3900.0 nM 5.41 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