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Compound Detail

CHEMBL4456725

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COc1ccc(S(=O)(=O)N(CC(C)C)C[C@@H](O)[C@H](Cc2ccccc2)Nc2c(N(C)[C@H]3CO[C@H]4OCC[C@H]43)c(=O)c2=O)cc1

Basic Information

ChEMBL ID CHEMBL4456725
Phase Preclinical
Structure Type MOL
InChI Key SVYFHKDGNIHBPM-AFZVTQHXSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

627.8
MW (Da)
2.22
ALogP
10
HBA
2
HBD
134.7
PSA (Ų)
0.26
QED
1
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H41N3O8S
MW 627.76
Aromatic Rings 3
Heavy Atoms 44
NP-Likeness -0.19

Activity Summary

Ki 1 meas. best 8.35

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 8.35 8.35 4.5 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 4.5 nM 8.35 Inhibition of HIV1 protease using Ac-Thr-Ile-Nle-Nle-Gln-Arg-NH2 substrate by co... 31416666

Literature References

PubMed DOI Target Context # Activities
31416666 10.1016/j.bmcl.2019.08.006 Human immunodeficiency virus 1 1
31416666 10.1016/j.bmcl.2019.08.006 Protease 1

Data from ChEMBL 36 via Core Engine