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Compound Detail

CHEMBL487435

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

Basic Information

ChEMBL ID CHEMBL487435
Phase Preclinical
Structure Type MOL
InChI Key BIJUDPHLIRJQPE-YDFBLROQSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

455.6
MW (Da)
3.13
ALogP
5
HBA
5
HBD
141.8
PSA (Ų)
0.37
QED
0
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H33N3O5
MW 455.56
Aromatic Rings 2
Heavy Atoms 33
NP-Likeness -0.37

Activity Summary

Ki 2 meas. best 4.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase N
CHEMBL1907
Ki 4.16 4.16 69000.0 1
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 4.12 4.12 76000.0 1

Activity Data Samples

Top measurements by pChEMBL value

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