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Compound Detail

CHEMBL4105142

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CC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](Cc1ccc(I)cc1)C(=O)N[C@@H](Cc1ccc(-c2ccccc2)cc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL4105142
Phase Preclinical
Structure Type MOL
InChI Key HCBZSDSBYHCIQA-RTNMLALUSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

867.8
MW (Da)
0.71
ALogP
7
HBA
11
HBD
283.3
PSA (Ų)
0.03
QED
2
Ro5 Violations
21
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H50IN11O5
MW 867.79
Aromatic Rings 3
Heavy Atoms 55
NP-Likeness -0.19

Activity Summary

Kd 2 meas. best 5.8
EC50 1 meas. best 5.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL3719
Kd 5.8 5.8 1584.9 1
Melanocortin receptor 5
CHEMBL4489
EC50 5.3 5.3 5000.0 1
Melanocortin receptor 3
CHEMBL4774
Kd 5.3 5.3 5011.9 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
28453292 10.1021/acs.jmedchem.7b00301 Melanocortin receptor 3 2
28453292 10.1021/acs.jmedchem.7b00301 Melanocortin receptor 4 2
28453292 10.1021/acs.jmedchem.7b00301 Melanocyte-stimulating hormone receptor 1
28453292 10.1021/acs.jmedchem.7b00301 Melanocortin receptor 5 1

Data from ChEMBL 36 via Core Engine