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Compound Detail

CHEMBL4437581

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CCOc1c(N[C@@H](Cc2ccccc2)[C@H](O)CN(CC(C)C)S(=O)(=O)c2ccc(OC)cc2)c(=O)c1=O

Basic Information

ChEMBL ID CHEMBL4437581
Phase Preclinical
Structure Type MOL
InChI Key OEDBXTXXZZVDNF-XZOQPEGZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

530.6
MW (Da)
2.42
ALogP
8
HBA
2
HBD
122.2
PSA (Ų)
0.30
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 C27H34N2O7S
MW 530.64
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -0.57

Activity Summary

Ki 1 meas. best 6.33

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 6.33 6.33 463.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 463.3 nM 6.33 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