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Compound Detail

CHEMBL451423

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CC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

Basic Information

ChEMBL ID CHEMBL451423
Phase Preclinical
Structure Type BOTH
InChI Key KCIDBIZAMUCOIJ-FKWFRFQNSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

730.8
MW (Da)
-0.47
ALogP
9
HBA
10
HBD
309.0
PSA (Ų)
0.02
QED
2
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H42N12O7
MW 730.79
Aromatic Rings 4
Heavy Atoms 53
NP-Likeness -0.29

Activity Summary

EC50 4 meas. best 7.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL3719
EC50 7.89 7.89 13.0 1
Melanocortin receptor 5
CHEMBL4489
EC50 7.75 7.75 17.6 1
Melanocortin receptor 3
CHEMBL4774
EC50 6.21 6.21 615.0 1
Melanocyte-stimulating hormone receptor
CHEMBL4077
EC50 5.99 5.99 1030.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18800761 10.1021/jm800291b Melanocyte-stimulating hormone receptor 2
18800761 10.1021/jm800291b Melanocortin receptor 3 2
18800761 10.1021/jm800291b Melanocortin receptor 4 2
18800761 10.1021/jm800291b Melanocortin receptor 5 2

Data from ChEMBL 36 via Core Engine