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Compound Detail

CHEMBL330561

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CC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

Basic Information

ChEMBL ID CHEMBL330561
Phase Preclinical
Structure Type BOTH
InChI Key ULBOINVSOBKOSI-ZXYZSCNASA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

701.9
MW (Da)
0.76
ALogP
7
HBA
8
HBD
239.7
PSA (Ų)
0.04
QED
2
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H43N9O5S
MW 701.85
Aromatic Rings 4
Heavy Atoms 50
NP-Likeness -0.20

Activity Summary

EC50 4 meas. best 7.39

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 5
CHEMBL4489
EC50 7.39 7.39 40.5 1
Melanocortin receptor 4
CHEMBL3719
EC50 7.04 7.04 91.2 1
Melanocyte-stimulating hormone receptor
CHEMBL4077
EC50 6.69 6.69 203.0 1
Melanocortin receptor 3
CHEMBL4774
EC50 5.53 5.53 2950.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
12061882 10.1021/jm0104872 Melanocyte-stimulating hormone receptor 1
12061882 10.1021/jm0104872 Melanocortin receptor 3 1
12061882 10.1021/jm0104872 Melanocortin receptor 4 1
12061882 10.1021/jm0104872 Melanocortin receptor 5 1

Data from ChEMBL 36 via Core Engine