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Compound Detail

CHEMBL2164935

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Cc1cc(C(=O)N[C@H](C(=O)N[C@@H](Cc2ccc(F)cc2)C(=O)N[C@@H](/C=C/C(=O)OCc2ccnc3ccccc23)CCC(N)=O)C(C)C)no1

Basic Information

ChEMBL ID CHEMBL2164935
Phase Preclinical
Structure Type MOL
InChI Key ZWZVIAQVWZFRBG-QPQAHCDJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

686.7
MW (Da)
3.20
ALogP
9
HBA
4
HBD
195.6
PSA (Ų)
0.10
QED
1
Ro5 Violations
16
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H39FN6O7
MW 686.74
Aromatic Rings 4
Heavy Atoms 50
NP-Likeness -0.63

Activity Summary

IC50 1 meas. best 6.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Genome polyprotein
CHEMBL2396505
IC50 6.89 6.89 130.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Genome polyprotein IC50 = 130.0 nM 6.89 Inhibition of Coxsackievirus B3 protease 3c using NMA-EALFQGPPVK-DNP as substrat... 23062551

Literature References

PubMed DOI Target Context # Activities
23062551 10.1016/j.bmcl.2012.08.120 Coxsackievirus B3 2
23062551 10.1016/j.bmcl.2012.08.120 Genome polyprotein 1

Data from ChEMBL 36 via Core Engine