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Compound Detail

CHEMBL1077585

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CCCC[C@@H](N)CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](C(=O)N[C@H]1Cc2c([nH]c3ccccc23)CN(CC(=O)N[C@@H](Cc2ccccc2)C(=O)O)C1=O)[C@@H](C)CC

Basic Information

ChEMBL ID CHEMBL1077585
Phase Preclinical
Structure Type MOL
InChI Key FYNOOCOLTPIGMJ-CNCKBNBHSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

824.0
MW (Da)
3.22
ALogP
8
HBA
8
HBD
236.1
PSA (Ų)
0.07
QED
2
Ro5 Violations
20
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C45H57N7O8
MW 823.99
Aromatic Rings 4
Heavy Atoms 60
NP-Likeness 0.07

Activity Summary

Ki 2 meas. best 7.26

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase N
CHEMBL1907
Ki 7.26 7.26 55.0 1
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 5.4 5.4 3981.1 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19757839 10.1021/jm900651p Aminopeptidase N 2
19757839 10.1021/jm900651p Leucyl-cystinyl aminopeptidase 2
19757839 10.1021/jm900651p Unchecked 1
19757839 10.1021/jm900651p Type-1 angiotensin II receptor 1
19757839 10.1021/jm900651p ADMET 1

Data from ChEMBL 36 via Core Engine