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Compound Detail

CHEMBL152612

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CC(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC(Cc1c[nH]c2ccccc12)C(N)=O

Basic Information

ChEMBL ID CHEMBL152612
Phase Preclinical
Structure Type MOL
InChI Key DFCJPPDAOZROBS-YFTKSLQMSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

685.8
MW (Da)
-0.58
ALogP
7
HBA
9
HBD
268.4
PSA (Ų)
0.04
QED
2
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H43N11O5
MW 685.79
Aromatic Rings 4
Heavy Atoms 50
NP-Likeness 0.12

Activity Summary

EC50 4 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanocortin receptor 5
CHEMBL4489
EC50 8.4 8.4 4.0 1
Melanocortin receptor 4
CHEMBL3719
EC50 7.76 7.76 17.2 1
Melanocyte-stimulating hormone receptor
CHEMBL4077
EC50 7.7 7.7 20.1 1
Melanocortin receptor 3
CHEMBL4774
EC50 6.81 6.81 156.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
12477357 10.1021/jm020296e Melanocyte-stimulating hormone receptor 1
12477357 10.1021/jm020296e Melanocortin receptor 3 1
12477357 10.1021/jm020296e Melanocortin receptor 4 1
12477357 10.1021/jm020296e Melanocortin receptor 5 1

Data from ChEMBL 36 via Core Engine