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Compound Detail

CHEMBL4060839

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COc1ccc(S(=O)(=O)N(CC(C)C)C[C@@H](O)[C@H](Cc2ccccc2)NC(=O)c2cncc(C(=O)N3CCC[C@@H]3c3nc(C)cs3)c2)cc1

Basic Information

ChEMBL ID CHEMBL4060839
Phase Preclinical
Structure Type MOL
InChI Key FHZVRJLISTWTAA-WIHCDAFUSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

705.9
MW (Da)
4.88
ALogP
9
HBA
2
HBD
142.0
PSA (Ų)
0.19
QED
1
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H43N5O6S2
MW 705.90
Aromatic Rings 4
Heavy Atoms 49
NP-Likeness -1.01

Activity Summary

Ki 1 meas. best 8.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 8.6 8.6 2.5 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 2.5 nM 8.6 Inhibition of HIV1 protease using fluorogenic substrate by continuous fluorometr... 28434781

Literature References

PubMed DOI Target Context # Activities
28434781 10.1016/j.bmc.2017.04.005 Unchecked 1
28434781 10.1016/j.bmc.2017.04.005 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine