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Compound Detail

CHEMBL233649

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CSCC[C@H](NC(=O)[C@@H](NC(=O)[C@H]1N(C(=O)[C@@H](O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(C)=O)C(C)C)CSC1(C)C)C(C)C)C(N)=O

Basic Information

ChEMBL ID CHEMBL233649
Phase Preclinical
Structure Type MOL
InChI Key LXYGCMDJKMGFGW-BJFASDGLSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

837.1
MW (Da)
-0.47
ALogP
11
HBA
8
HBD
272.2
PSA (Ų)
0.07
QED
3
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H60N8O9S2
MW 837.08
Aromatic Rings 1
Heavy Atoms 57
NP-Likeness 0.12

Activity Summary

IC50 1 meas. best 6.45

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Gag-Pro polyprotein
CHEMBL3346
IC50 6.45 6.45 353.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Gag-Pro polyprotein IC50 = 353.0 nM 6.45 Inhibition of HTLV1 protease L40I mutant expressed in Escherichia coli BL21(DE3)... 18006315

Literature References

PubMed DOI Target Context # Activities
17448657 10.1016/j.bmcl.2007.04.019 Unchecked 2
18006315 10.1016/j.bmcl.2007.10.066 Protease 1
18006315 10.1016/j.bmcl.2007.10.066 Gag-Pro polyprotein 1

Data from ChEMBL 36 via Core Engine