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Compound Detail

CHEMBL3085804

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CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL3085804
Phase Preclinical
Structure Type MOL
InChI Key GRKFAKKVJNTEAI-UHXSMRHISA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

1317.5
MW (Da)

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C63H84N18O14
MW 1317.48

Activity Summary

Ki 2 meas. best 10.28

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KiSS-1 receptor
CHEMBL5413
Ki 10.28 10.28 0.1 1
KiSS-1 receptor
CHEMBL1169599
Ki 10.15 10.15 0.1 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KiSS-1 receptor Ki = 0.052 nM 10.28 Binding affinity to human KISS1R expressed in CHO cell membranes 24047141
KiSS-1 receptor Ki = 0.07 nM 10.15 Binding affinity to rat KISS1R 24047141

Literature References

PubMed DOI Target Context # Activities
24047141 10.1021/jm401056w KiSS-1 receptor 3
24047141 10.1021/jm401056w Serum 1

Data from ChEMBL 36 via Core Engine