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Compound Detail

CHEMBL4174361

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CCCC[C@@H]1NC(=O)[C@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O

Basic Information

ChEMBL ID CHEMBL4174361
Phase Preclinical
Structure Type MOL
InChI Key JOKDUJYLRRCMRY-PZMAVKSXSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

957.1
MW (Da)
-0.88
ALogP
10
HBA
10
HBD
320.2
PSA (Ų)
0.06
QED
2
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C48H68N12O9
MW 957.15
Aromatic Rings 2
Heavy Atoms 69
NP-Likeness 0.54

Activity Summary

Kd 2 meas. best 8.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL3719
Kd 8.6 8.6 2.5 1
Melanocortin receptor 3
CHEMBL4774
Kd 6.2 6.2 631.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
30035543 10.1021/acs.jmedchem.8b00684 Melanocortin receptor 5 2
30035543 10.1021/acs.jmedchem.8b00684 Melanocyte-stimulating hormone receptor 2
30035543 10.1021/acs.jmedchem.8b00684 Melanocortin receptor 4 2
30035543 10.1021/acs.jmedchem.8b00684 Melanocortin receptor 3 2
30035543 10.1021/acs.jmedchem.8b00684 Unchecked 1

Data from ChEMBL 36 via Core Engine