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Compound Detail

CHEMBL272494

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CC[C@H](C)[C@H](NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N1CSC(C)(C)[C@@H]1C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(N)=O)[C@@H](C)CC)c1ccccc1

Basic Information

ChEMBL ID CHEMBL272494
Phase Preclinical
Structure Type MOL
InChI Key PBACNDIAGMYTTF-OPXQPRFUSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

870.1
MW (Da)
2.42
ALogP
10
HBA
7
HBD
229.1
PSA (Ų)
0.09
QED
2
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H63N7O8S2
MW 870.15
Aromatic Rings 2
Heavy Atoms 60
NP-Likeness -0.01

Activity Summary

IC50 1 meas. best 6.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Gag-Pro polyprotein
CHEMBL3346
IC50 6.5 6.5 320.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Gag-Pro polyprotein IC50 = 320.0 nM 6.5 Inhibition of HTLV1 protease L40I mutant expressed in Escherichia coli BL21(DE3)... 18006315

Literature References

PubMed DOI Target Context # Activities
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