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Compound Detail

CHEMBL469484

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CC[C@@H](C)[C@H](NC(=O)c1cc(N)cc(Cc2ccc(O)cc2)c1)C(=O)NCc1ccccc1CC(=O)O

Basic Information

ChEMBL ID CHEMBL469484
Phase Preclinical
Structure Type MOL
InChI Key ICAOSNPQNLVFDW-CLYVBNDRSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

503.6
MW (Da)
3.65
ALogP
5
HBA
5
HBD
141.8
PSA (Ų)
0.25
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H33N3O5
MW 503.60
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -0.52

Activity Summary

Ki 1 meas. best 4.01

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 4.01 4.01 97000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Leucyl-cystinyl aminopeptidase Ki = 97000.0 nM 4.01 Inhibition of human recombinant IRAP expressed in HEK293 cells 18556208

Literature References

PubMed DOI Target Context # Activities
18556208 10.1016/j.bmc.2008.05.046 Leucyl-cystinyl aminopeptidase 2
18556208 10.1016/j.bmc.2008.05.046 Aminopeptidase N 1

Data from ChEMBL 36 via Core Engine