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Compound Detail

CHEMBL264352

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CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H]1CSSC[C@H](C(N)=O)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@@H](CCC(=O)O)NC1=O

Basic Information

ChEMBL ID CHEMBL264352
Phase Preclinical
Structure Type BOTH
InChI Key FEKXKTLLBDRSQH-XVRHLUALSA-N
4
Targets
5
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

1338.5
MW (Da)

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C60H79N19O13S2
MW 1338.55

Activity Summary

Ki 4 meas. best 9.28
EC50 1 meas. best 9.57

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL259
EC50 9.57 9.57 0.3 1
Melanocortin receptor 4
CHEMBL2700
Ki 9.28 9.28 0.5 1
Melanocortin receptor 4
CHEMBL259
Ki 9.11 9.11 0.8 1
Melanocyte-stimulating hormone receptor
CHEMBL3795
Ki 7.77 7.77 17.1 1
Melanocortin receptor 3
CHEMBL4644
Ki 7.26 7.26 55.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15857110 10.1021/jm0501432 Melanocortin receptor 4 4
15857110 10.1021/jm0501432 Melanocyte-stimulating hormone receptor 1
15857110 10.1021/jm0501432 Melanocortin receptor 3 1
15857110 10.1021/jm0501432 Melanocortin receptor 5 1

Data from ChEMBL 36 via Core Engine