Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2114365

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CC(C)C[C@@H](N)C(=O)CC(Cc1ccccc1)C(=O)O

Basic Information

ChEMBL ID CHEMBL2114365
Phase Preclinical
Structure Type MOL
InChI Key SGMZGZICZKFASN-ARLHGKGLSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

277.4
MW (Da)
2.26
ALogP
3
HBA
2
HBD
80.4
PSA (Ų)
0.76
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H23NO3
MW 277.36
Aromatic Rings 1
Heavy Atoms 20
NP-Likeness 0.51

Activity Summary

Ki 2 meas. best 6.11

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase B
CHEMBL2452
Ki 6.11 6.11 770.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Aminopeptidase B Ki = 770.0 nM 6.11 Competitive inhibition of aminopeptidase B or arginyl aminopeptidase purified fr... 2566685

Literature References

PubMed DOI Target Context # Activities
2566685 10.1021/jm00126a039 Leucyl-cystinyl aminopeptidase 2
2566685 10.1021/jm00126a039 Aminopeptidase B 1

Data from ChEMBL 36 via Core Engine