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Compound Detail

CHEMBL5093125

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C#CC[C@H](NCCC)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCc1ccc(-c2ccccc2)cc1

Basic Information

ChEMBL ID CHEMBL5093125
Phase Preclinical
Structure Type MOL
InChI Key NUCRAMFEBUKPJM-KYJUHHDHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

506.6
MW (Da)
4.57
ALogP
3
HBA
4
HBD
86.0
PSA (Ų)
0.21
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H34N4O2
MW 506.65
Aromatic Rings 4
Heavy Atoms 38
NP-Likeness -0.48

Activity Summary

IC50 1 meas. best 4.64

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.64 4.64 22650.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 22650.0 nM 4.64 Inhibition of SARS CoV-2 main protease using DABCYL-KTSAVLQ1SGFRKM-E(EDANS)-NH2 ... 34571172

Literature References

PubMed DOI Target Context # Activities
34571172 10.1016/j.ejmech.2021.113863 Unchecked 2
34571172 10.1016/j.ejmech.2021.113863 SARS-CoV-2 2
34571172 10.1016/j.ejmech.2021.113863 Vero 2

Data from ChEMBL 36 via Core Engine