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Compound Detail

CHEMBL4467544

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

Basic Information

ChEMBL ID CHEMBL4467544
Phase Preclinical
Structure Type MOL
InChI Key XDNRBKBBLUFFJU-WLQDXNQPSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

613.7
MW (Da)
2.20
ALogP
10
HBA
3
HBD
143.5
PSA (Ų)
0.23
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 C31H39N3O8S
MW 613.73
Aromatic Rings 3
Heavy Atoms 43
NP-Likeness -0.18

Activity Summary

Ki 1 meas. best 8.25

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 8.25 8.25 5.6 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 5.6 nM 8.25 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