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Compound Detail

CHEMBL448184

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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)NCc1ccccc1CC(=O)O

Basic Information

ChEMBL ID CHEMBL448184
Phase Preclinical
Structure Type MOL
InChI Key QYODAZQUNPNFRP-VHOLSGDPSA-N
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

602.7
MW (Da)
3.99
ALogP
6
HBA
6
HBD
170.8
PSA (Ų)
0.16
QED
2
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H42N4O6
MW 602.73
Aromatic Rings 3
Heavy Atoms 44
NP-Likeness -0.53

Activity Summary

Ki 3 meas. best 5.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 5.89 5.47 1300.0 2
Aminopeptidase N
CHEMBL1907
Ki 4.68 4.68 21000.0 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