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Assay Detail

CHEMBL1663824

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

Binding
Inhibition of rat SK Calcium channel
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Discovery of {1-[4-(2-{hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}-1H-benzimidazol-1-yl)piperidin-1-yl]cyclooctyl}methanol, systemically potent novel non-peptide agonist of nociceptin/orphanin FQ receptor as analgesic for the treatment of neuropathic pain: design, synthesis, and structure-activity relationships.
Hayashi S, Nakata E, Morita A, Mizuno K, Yamamura K, Kato A, Ohashi K.
Bioorg Med Chem (2010) 18 : 7675 -7699
PubMed 20875743 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 10.62 10.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL525408 APAMIN 1 10.62

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL525408 APAMIN IC50 = 0.024 nM 10.62