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Assay Detail

CHEMBL4714818

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

Binding
Inhibition of 5-[[(1r,4r)-4-[[(1S)-4-amino-1-[[(1S,2R)-1-[[(1S)-2-[[(1S)-1-[[(1S)-1-[[(1S)-2-[[(1S,2R)-1-[[2-(carboxymethylamino)-2-oxoethyl]carbamoyl]-2-hydroxypropyl]amino]-1-(hydroxymethyl)-2-oxoethyl]carbamoyl]-5-[3-[N-methyl-4-[(4-nitrophenyl)azo]anilino]propanoylamino]pentyl]carbamoyl]-4-guanidinobutyl]amino]-1-methyl-2-oxoethyl]carbamoyl]-2-hydroxypropyl]carbamoyl]-4-oxobutyl]carbamoyl]cyclohexyl]carbamothioylamino]-2-(3-hydroxy-6-oxoxanthen-9-yl)benzoic acid binding to SIRT2 (unknown origin) measured after 2 hrs in presence of NAD+ by fluorometric method
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

NAD-dependent protein deacetylase sirtuin-2 (CHEMBL4462)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A Set of Highly Sensitive Sirtuin Fluorescence Probes for Screening Small-Molecular Sirtuin Defatty-Acylase Inhibitors.
Nakajima Y,Kawaguchi M,Ieda N,Nakagawa H
ACS Med Chem Lett (2021) 12 : 617 -624
PubMed 33859801 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.00 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4438193 1 7.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4438193 IC50 = 100.0 nM 7.00