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Compound Detail

CHEMBL1161323

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CCCC[C@@H](NC(C)=O)C(=O)N[C@@H]1CC(=O)NCCCC[C@@H](C(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H]2C[C@@]3(C)CCCC[C@@]3(C)N2C1=O

Basic Information

ChEMBL ID CHEMBL1161323
Phase Preclinical
Structure Type BOTH
InChI Key KHGZKFBKKYRZCD-FFQWDCJVSA-N
3
Targets
6
Activities
3
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

1116.4
MW (Da)

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C59H81N13O9
MW 1116.38

Activity Summary

IC50 3 meas. best 9.96
Kd 2 meas. best 8.9
EC50 1 meas. best 9.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 5
CHEMBL4608
IC50 9.96 9.96 0.1 1
Melanocortin receptor 4
CHEMBL259
IC50 9.8 9.8 0.2 1
Melanocortin receptor 5
CHEMBL4608
EC50 9.7 9.7 0.2 1
Melanocortin receptor 4
CHEMBL259
Kd 8.9 8.9 1.3 1
Melanocortin receptor 3
CHEMBL4644
IC50 8.6 8.6 2.5 1
Melanocortin receptor 3
CHEMBL4644
Kd 8.2 8.2 6.3 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
12431055 10.1021/jm0202526 Melanocortin receptor 3 3
12431055 10.1021/jm0202526 Melanocortin receptor 4 3
12431055 10.1021/jm0202526 Melanocortin receptor 5 3

Data from ChEMBL 36 via Core Engine