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Compound Detail

CHEMBL82898

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C[C@H](NC(=O)[C@@H](CC(=O)O)Cc1ccccc1)C(=O)O

Basic Information

ChEMBL ID CHEMBL82898
Phase Preclinical
Structure Type MOL
InChI Key ZQIDVTXWUJKSQE-GXSJLCMTSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

279.3
MW (Da)
0.91
ALogP
3
HBA
3
HBD
103.7
PSA (Ų)
0.69
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 C14H17NO5
MW 279.29
Aromatic Rings 1
Heavy Atoms 20
NP-Likeness 0.03

Activity Summary

IC50 2 meas. best 6.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.85 6.85 140.0 1
Leukotriene A-4 hydrolase
CHEMBL4618
IC50 6.52 6.52 300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 140.0 nM 6.85 Inhibitory activity against aminopeptidase -
Leukotriene A-4 hydrolase IC50 = 300.0 nM 6.52 Inhibitory activity against recombinant human Leukotriene A4 hydrolase -

Literature References

PubMed DOI Target Context # Activities
- 10.1016/0960-894X(95)00441-U Leukotriene A-4 hydrolase 1
- 10.1016/0960-894X(95)00441-U Unchecked 1
- 10.1016/0960-894X(95)00441-U Angiotensin-converting enzyme 1

Data from ChEMBL 36 via Core Engine