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Compound Detail

CHEMBL450236

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CCC[C@H]1C(=O)N([C@@H](Cc2ccc3ccccc3c2)C(=O)NC)CCN1C(=O)[C@@H](Cc1ccc(F)cc1)NC(=O)C1(N)CCCC1

Basic Information

ChEMBL ID CHEMBL450236
Phase Preclinical
Structure Type MOL
InChI Key WOWDZBDFXRWMIV-AYQJTBPPSA-N
3
Targets
6
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

629.8
MW (Da)
3.47
ALogP
5
HBA
3
HBD
124.8
PSA (Ų)
0.30
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H44FN5O4
MW 629.78
Aromatic Rings 3
Heavy Atoms 46
NP-Likeness -0.20

Activity Summary

EC50 3 meas. best 8.05
Ki 3 meas. best 7.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 4
CHEMBL259
EC50 8.05 8.05 9.0 1
Melanocortin receptor 4
CHEMBL259
Ki 7.85 7.85 14.0 1
Melanocyte-stimulating hormone receptor
CHEMBL3795
EC50 7.36 7.36 44.0 1
Melanocortin receptor 3
CHEMBL4644
EC50 7.24 7.24 58.0 1
Melanocyte-stimulating hormone receptor
CHEMBL3795
Ki 6.65 6.65 225.0 1
Melanocortin receptor 3
CHEMBL4644
Ki 6.33 6.33 471.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18771254 10.1021/jm800525p Melanocortin receptor 3 3
18771254 10.1021/jm800525p Melanocortin receptor 4 3
18771254 10.1021/jm800525p Melanocyte-stimulating hormone receptor 3

Data from ChEMBL 36 via Core Engine