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Compound Detail

CHEMBL1077590

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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)N1Cc2ccccc2C[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O

Basic Information

ChEMBL ID CHEMBL1077590
Phase Preclinical
Structure Type BOTH
InChI Key HBTKHGJMLKXJGS-XZUOCMGYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

797.0
MW (Da)
2.69
ALogP
8
HBA
6
HBD
211.5
PSA (Ų)
0.13
QED
2
Ro5 Violations
16
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H56N6O8
MW 796.97
Aromatic Rings 3
Heavy Atoms 58
NP-Likeness -0.10

Activity Summary

Ki 2 meas. best 6.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase N
CHEMBL1907
Ki 6.66 6.66 218.8 1
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 5.61 5.61 2454.7 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

Data from ChEMBL 36 via Core Engine