Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5372997

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Displacement of [3H]-(9S,12S,15S,19R,E)-4-amino-N-((S)-1-(((S)-1-(((S)-1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)amino)-5-guanidino-1-oxopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)-15-(3-guanidinopropyl)-12-(4-hydroxybenzyl)-2,11,14,17,20-pentaoxo-19-(4-(propanamido-2,3-t2)butanamido)-1,3,5,10,13,16,21-heptaazacyclopentacos-3-ene-9-carboxamide from human Y4R expressed in CHO cells coexpressing Gqi5-mtAEQ under hypotonic sodium free buffer condition
10
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Neuropeptide Y receptor type 4 (CHEMBL4877)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

[<sup>3</sup>H]UR-JG102-A Radiolabeled Cyclic Peptide with High Affinity and Excellent Selectivity for the Neuropeptide Y Y<sub>4</sub> Receptor.
Gleixner J, Gattor AO, Humphrys LJ, Brunner T, Keller M.
J Med Chem (2023) 66 : 13788 -13808
PubMed 37773891 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 10.09 11.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5423253 2 11.00
CHEMBL4873376 2 10.96
CHEMBL4540843 PANCREATIC POLYPEPTIDE 2.0 2 10.44
CHEMBL5428989 2 9.68
CHEMBL5411178 2 9.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5423253 Ki = 0.01 nM 11.00
CHEMBL4873376 Ki = 0.011 nM 10.96
CHEMBL4540843 PANCREATIC POLYPEPTIDE Ki = 0.03631 nM 10.44
CHEMBL4540843 PANCREATIC POLYPEPTIDE Ki = 0.037 nM 10.43
CHEMBL5428989 Ki = 0.2089 nM 9.68
CHEMBL5411178 Ki = 0.389 nM 9.41
CHEMBL5411178 Ki = 0.39 nM 9.41
CHEMBL5428989 Ki = 0.41 nM 9.39
CHEMBL5423253 Ki = 0.008913 nM -
CHEMBL4873376 Ki = 0.00912 nM -