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Compound Detail

CHEMBL267659

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CC(=O)NC(CS(=O)(=O)c1cccc2ccccc12)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N1CSC(C)(C)[C@H]1C(=O)NCc1ccccc1C

Basic Information

ChEMBL ID CHEMBL267659
Phase Preclinical
Structure Type MOL
InChI Key NYWNZCXQNAGWLE-XTUXAWACSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

744.9
MW (Da)
3.51
ALogP
8
HBA
4
HBD
162.0
PSA (Ų)
0.16
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H44N4O7S2
MW 744.94
Aromatic Rings 4
Heavy Atoms 52
NP-Likeness -0.21

Activity Summary

EC50 1 meas. best 7.4
IC50 1 meas. best 10.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 10.05 10.05 0.1 1
Human immunodeficiency virus 1
CHEMBL378
EC50 7.4 7.4 40.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 0.09 nM 10.05 Inhibition of HIV protease 17537628
Human immunodeficiency virus 1 EC50 = 40.0 nM 7.4 Antiviral activity against HIV1 3B in MT4 cells by MTT assay 17537628

Literature References

PubMed DOI Target Context # Activities
17537628 10.1016/j.bmcl.2007.05.039 Unchecked 3
17537628 10.1016/j.bmcl.2007.05.039 Human immunodeficiency virus 1 1
17537628 10.1016/j.bmcl.2007.05.039 MT4 1

Data from ChEMBL 36 via Core Engine