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Compound Detail

CHEMBL259039

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COC(=O)N[C@H](C(=O)NN(CCC[C@](O)(Cc1ccccc1)C(=O)N[C@H]1c2ccccc2C[C@H]1O)Cc1ccc(Br)cc1)C(C)(C)C

Basic Information

ChEMBL ID CHEMBL259039
Phase Preclinical
Structure Type MOL
InChI Key BUXZHPPMFKNUOP-RKVFUFCESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

709.7
MW (Da)
4.58
ALogP
7
HBA
5
HBD
140.2
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 C36H45BrN4O6
MW 709.68
Aromatic Rings 3
Heavy Atoms 47
NP-Likeness 0.05

Activity Summary

Ki 1 meas. best 6.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 6.38 6.38 420.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 420.0 nM 6.38 Inhibition of HIV1 protease expressed in Escherichia coli 18215014

Literature References

PubMed DOI Target Context # Activities
18215014 10.1021/jm070680h Protease 1
18215014 10.1021/jm070680h Human immunodeficiency virus 1 1
18215014 10.1021/jm070680h MT4 1
18215014 10.1021/jm070680h Caco-2 1

Data from ChEMBL 36 via Core Engine