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Compound Detail

CHEMBL526298

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C[C@H](CS)C(=O)N1[C@@H](SCCc2ccccc2)CC[C@H]1C(=O)O

Basic Information

ChEMBL ID CHEMBL526298
Phase Preclinical
Structure Type MOL
InChI Key QVHZTNDYZCMLFE-SNPRPXQTSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

353.5
MW (Da)
2.93
ALogP
4
HBA
2
HBD
57.6
PSA (Ų)
0.74
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H23NO3S2
MW 353.51
Aromatic Rings 1
Heavy Atoms 23
NP-Likeness 0.02

Activity Summary

IC50 2 meas. best 9.74

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Angiotensin-converting enzyme
CHEMBL1808
IC50 9.74 9.74 0.2 1
Leukotriene A-4 hydrolase
CHEMBL5786
IC50 5.29 5.29 5100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Angiotensin-converting enzyme IC50 = 0.18 nM 9.74 Inhibition of ACE 18674901
Leukotriene A-4 hydrolase IC50 = 5100.0 nM 5.29 Inhibition of guinea pig lung leukotriene A4 hydrolase 18674901

Literature References

PubMed DOI Target Context # Activities
18674901 10.1016/j.bmcl.2008.07.043 Leukotriene A-4 hydrolase 1
18674901 10.1016/j.bmcl.2008.07.043 Angiotensin-converting enzyme 1

Data from ChEMBL 36 via Core Engine