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Compound Detail

CHEMBL271878

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CC[C@H](C)[C@H](NC(=O)[C@@H]1N(C(=O)[C@@H](O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@@H](NC(C)=O)c2ccccc2)C(C)(C)C)CSC1(C)C)C(=O)N[C@@H](CCSC)C(N)=O

Basic Information

ChEMBL ID CHEMBL271878
Phase Preclinical
Structure Type MOL
InChI Key AMXJIKRNCOHDNZ-CODVFHOUSA-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)
0.10
QED
2
Ro5 Violations
20
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 0.21

Activity Summary

IC50 1 meas. best 7.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Gag-Pro polyprotein
CHEMBL3346
IC50 7.0 7.0 101.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Gag-Pro polyprotein IC50 = 101.0 nM 7.0 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