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Compound Detail

CHEMBL5278854

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CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(=O)O)C(=O)O

Basic Information

ChEMBL ID CHEMBL5278854
Phase Preclinical
Structure Type MOL
InChI Key NHJUFNWIIVOTIH-NUDUWCFGSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

1243.4
MW (Da)

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C55H86N16O17
MW 1243.39

Activity Summary

IC50 2 meas. best 6.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
PCSK9/LDLR
CHEMBL4523996
IC50 6.16 6.16 700.0 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
IC50 4.05 4.05 88900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
36446632 10.1021/acs.jmedchem.2c01290 PCSK9/LDLR 3
36446632 10.1021/acs.jmedchem.2c01290 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1

Data from ChEMBL 36 via Core Engine