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Compound Detail

CHEMBL501326

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CC(C)[C@H](N)C(=O)Nc1cc(Cc2ccc(O)cc2)cc(C(=O)N2CCC[C@H]2C(=O)NCc2ccccc2C(=O)O)c1

Basic Information

ChEMBL ID CHEMBL501326
Phase Preclinical
Structure Type MOL
InChI Key YBYTVJPRGHOHDZ-NSOVKSMOSA-N
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

572.7
MW (Da)
3.52
ALogP
6
HBA
5
HBD
162.1
PSA (Ų)
0.25
QED
1
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H36N4O6
MW 572.66
Aromatic Rings 3
Heavy Atoms 42
NP-Likeness -0.78

Activity Summary

Ki 3 meas. best 4.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 4.92 4.905 12000.0 2
Aminopeptidase N
CHEMBL1907
Ki 4.26 4.26 55000.0 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