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

CHEMBL5553822

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

Binding
Inhibition of recombinant human haspin (470 to 798 residues) expressed in bacteria using ARTKQTARKSTGGKAPRKQLA as substrate incubated for 30 mins in presence of ATP by ADP-Glo kinase assay
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

Serine/threonine-protein kinase haspin (CHEMBL1075163)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A Comprehensive <i>In Vitro</i> Characterization of a New Class of Indole-Based Compounds Developed as Selective Haspin Inhibitors.
Vestuto V, Ciaglia T, Musella S, Di Sarno V, Smaldone G, Di Matteo F, Scala MC, Napolitano V, Miranda MR, Amodio G, Novi S, Pepe G, Basilicata MG, Gazzillo E, Pace S, Gomez-Monterrey IM, Sala M, Bifulco G, Tecce MF, Campiglia P, Ostacolo C, Lauro G, Manfra M, Bertamino A.
J Med Chem (2024) 67 : 12711 -12734
PubMed 39038808 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.18 7.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5181620 1 7.18

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5181620 IC50 = 65.8 nM 7.18