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Compound Detail

CHEMBL4174761

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N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CO)NC(=O)[C@H](CN)NC(=O)[C@H](CCc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC1=O

Basic Information

ChEMBL ID CHEMBL4174761
Phase Preclinical
Structure Type MOL
InChI Key YKHASWSLDVHIPY-JTPPURIGSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

979.1
MW (Da)
-1.78
ALogP
11
HBA
11
HBD
323.4
PSA (Ų)
0.05
QED
3
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C50H66N12O9
MW 979.15
Aromatic Rings 3
Heavy Atoms 71
NP-Likeness 0.50

Activity Summary

Kd 2 meas. best 9.2

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL3719
Kd 9.2 9.2 0.6 1
Melanocortin receptor 3
CHEMBL4774
Kd 7.2 7.2 63.1 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 Melanocortin receptor 4 2
30035543 10.1021/acs.jmedchem.8b00684 Melanocortin receptor 3 2
30035543 10.1021/acs.jmedchem.8b00684 Melanocyte-stimulating hormone receptor 1
30035543 10.1021/acs.jmedchem.8b00684 Unchecked 1

Data from ChEMBL 36 via Core Engine