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Compound Detail

CHEMBL4472672

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CCCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)NNC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)NC)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL4472672
Phase Preclinical
Structure Type MOL
InChI Key MELMLAHGMHGBKE-ORYMTKCHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

751.0
MW (Da)
1.26
ALogP
7
HBA
10
HBD
248.5
PSA (Ų)
0.04
QED
2
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H58N10O6
MW 750.95
Aromatic Rings 2
Heavy Atoms 54
NP-Likeness -0.16

Activity Summary

EC50 1 meas. best 8.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KiSS-1 receptor
CHEMBL5413
EC50 8.85 8.85 1.4 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KiSS-1 receptor EC50 = 1.4 nM 8.85 Agonist activity at human KISS1R expressed in CHO cells assessed as increase in ... 30598349

Literature References

PubMed DOI Target Context # Activities
30598349 10.1016/j.bmcl.2018.12.016 No relevant target 1
30598349 10.1016/j.bmcl.2018.12.016 KiSS-1 receptor 1

Data from ChEMBL 36 via Core Engine