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Compound Detail

CHEMBL1077592

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CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)C(C)C)C(=O)N[C@H]1Cc2ccccc2CN(CC(=O)N[C@@H](Cc2ccccc2)C(=O)O)C1=O

Basic Information

ChEMBL ID CHEMBL1077592
Phase Preclinical
Structure Type MOL
InChI Key IRVWFEPKJPEGIM-KBCQHTJQSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

756.9
MW (Da)
1.82
ALogP
8
HBA
7
HBD
220.3
PSA (Ų)
0.11
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H52N6O8
MW 756.90
Aromatic Rings 3
Heavy Atoms 55
NP-Likeness -0.02

Activity Summary

Ki 2 meas. best 7.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase N
CHEMBL1907
Ki 7.3 7.3 50.1 1
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 5.69 5.69 2041.7 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