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Compound Detail

CHEMBL258480

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CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC[C@H](CC(C)C)C(=O)O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)O

Basic Information

ChEMBL ID CHEMBL258480
Phase Preclinical
Structure Type BOTH
InChI Key GCFLCRJGOHZHEC-WRRKRXPISA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

804.0
MW (Da)
2.42
ALogP
9
HBA
8
HBD
243.2
PSA (Ų)
0.07
QED
2
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H57N7O9
MW 803.96
Aromatic Rings 3
Heavy Atoms 58
NP-Likeness -0.03

Activity Summary

Ki 2 meas. best 6.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Aminopeptidase N
CHEMBL1907
Ki 6.85 6.85 141.2 1
Leucyl-cystinyl aminopeptidase
CHEMBL2693
Ki 5.88 5.88 1318.3 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18386881 10.1021/jm701490g Leucyl-cystinyl aminopeptidase 1
18386881 10.1021/jm701490g Aminopeptidase N 1

Data from ChEMBL 36 via Core Engine