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Compound Detail

CHEMBL4206617

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COc1ccc(S(=O)(=O)N(CC(C)C)C[C@@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@@H]2C[C@@H]3CO[C@@H]4CCC[C@H]2[C@H]34)cc1

Basic Information

ChEMBL ID CHEMBL4206617
Phase Preclinical
Structure Type MOL
InChI Key YTIYICLVROYRNE-DATQEUORSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

600.8
MW (Da)
4.24
ALogP
7
HBA
2
HBD
114.4
PSA (Ų)
0.37
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H44N2O7S
MW 600.78
Aromatic Rings 2
Heavy Atoms 42
NP-Likeness 0.23

Activity Summary

Ki 1 meas. best 8.34

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 8.34 8.34 4.5 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 4.55 nM 8.34 Inhibition of wild type HIV-1 NL4-3 protease expressed in Escherichia coli Roset... 29763303

Literature References

PubMed DOI Target Context # Activities
29763303 10.1021/acs.jmedchem.8b00298 Protease 1
29763303 10.1021/acs.jmedchem.8b00298 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine