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Compound Detail

CHEMBL4103985

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CC(=O)N[C@@H](Cc1ccc(-c2ccccc2)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](Cc1ccc(I)cc1)C(=O)N[C@@H](Cc1csc2ccccc12)C(N)=O

Basic Information

ChEMBL ID CHEMBL4103985
Phase Preclinical
Structure Type MOL
InChI Key RCORIQNPILXJRC-MYOMABOUSA-N
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

914.9
MW (Da)
3.91
ALogP
7
HBA
8
HBD
221.4
PSA (Ų)
0.03
QED
2
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H47IN8O5S
MW 914.87
Aromatic Rings 5
Heavy Atoms 58
NP-Likeness -0.43

Activity Summary

EC50 3 meas. best 5.64

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 3
CHEMBL4774
EC50 5.64 5.64 2300.0 1
Melanocyte-stimulating hormone receptor
CHEMBL4077
EC50 5.51 5.51 3100.0 1
Melanocortin receptor 5
CHEMBL4489
EC50 5.26 5.26 5500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
28453292 10.1021/acs.jmedchem.7b00301 Melanocortin receptor 4 3
28453292 10.1021/acs.jmedchem.7b00301 Melanocortin receptor 3 1
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