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Compound Detail

CHEMBL211131

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N=C(N)NCCC[C@@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2c[nH]cn2)NC(=O)CCCCCCCNC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O

Basic Information

ChEMBL ID CHEMBL211131
Phase Preclinical
Structure Type MOL
InChI Key KYHILABVVZODQF-GZXHTMMISA-N
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

767.9
MW (Da)
1.59
ALogP
7
HBA
10
HBD
251.9
PSA (Ų)
0.06
QED
2
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C40H53N11O5
MW 767.94
Aromatic Rings 4
Heavy Atoms 56
NP-Likeness 0.42

Activity Summary

EC50 3 meas. best 9.28
Ki 1 meas. best 5.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor (M1 and M4)
CHEMBL2111423
EC50 9.28 9.28 0.5 1
Melanocortin receptor 4
CHEMBL259
Ki 5.36 5.36 4420.0 1
Melanocyte-stimulating hormone receptor
CHEMBL3795
EC50 5.29 5.29 5095.8 1
Melanocortin receptor 4
CHEMBL259
EC50 5.02 5.02 9592.4 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16678415 10.1016/j.bmcl.2006.04.050 Melanocortin receptor 4 2
16678415 10.1016/j.bmcl.2006.04.050 Melanocortin receptor (M1 and M4) 1
16678415 10.1016/j.bmcl.2006.04.050 Melanocyte-stimulating hormone receptor 1

Data from ChEMBL 36 via Core Engine