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Compound Detail

CHEMBL606392

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Cc1c(O)cccc1C(=O)N[C@@H](Cc1cccs1)[C@H](O)CN1C[C@H]2CCCC[C@H]2C[C@H]1C(=O)NC(C)(C)C

Basic Information

ChEMBL ID CHEMBL606392
Phase Preclinical
Structure Type MOL
InChI Key OTWIIQSIDGVCGR-WKFYBSLTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

541.8
MW (Da)
4.26
ALogP
6
HBA
4
HBD
101.9
PSA (Ų)
0.40
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H43N3O4S
MW 541.76
Aromatic Rings 2
Heavy Atoms 38
NP-Likeness -0.37

Activity Summary

IC50 1 meas. best 8.54

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 8.54 8.54 2.9 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 2.9 nM 8.54 Inhibition of recombinant wild type HIV1 protease assessed as hydrolysis of fluo... 20108932

Literature References

PubMed DOI Target Context # Activities
20108932 10.1021/jm900846f Protease 3
20108932 10.1021/jm900846f Human immunodeficiency virus type 1 protease 3

Data from ChEMBL 36 via Core Engine