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Assay Detail

CHEMBL1055471

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

Binding
Inhibition of wild type CXCR1 transfected in mouse L1.2 cells assessed as inhibition of CXCL8-induced cell migration pretreated for 15 mins measured after 4 hrs
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type L1.2
Confidence 8 — Homologous single protein target
Curated By Intermediate

Target

C-X-C chemokine receptor type 1 (CHEMBL4029)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Activity Relationship of novel phenylacetic CXCR1 inhibitors.
Sablone MR, Cesta MC, Moriconi A, Aramini A, Bizzarri C, Di Giacinto C, Di Bitondo R, Gloaguen I, Aschi M, Crucianelli M, Bertini R, Allegretti M.
Bioorg Med Chem Lett (2009) 19 : 4026 -4030
PubMed 19560921 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.92 7.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL139 DICLOFENAC 4.0 1 7.92

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL139 DICLOFENAC IC50 = 12.0 nM 7.92