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Assay Detail

CHEMBL828754

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

Binding
In vitro binding affinity was determined as displacement of [3H]N-R-methylhistamine from C6 cell membranes expressing human histamine H3 receptor
29
Total Activities
29
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type C6
Confidence 9 — Direct single protein target
Curated By Expert

Target

Histamine H3 receptor (CHEMBL264)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

4-(2-[2-(2(R)-methylpyrrolidin-1-yl)ethyl]benzofuran-5-yl)benzonitrile and related 2-aminoethylbenzofuran H3 receptor antagonists potently enhance cognition and attention.
Cowart M, Faghih R, Curtis MP, Gfesser GA, Bennani YL, Black LA, Pan L, Marsh KC, Sullivan JP, Esbenshade TA, Fox GB, Hancock AA.
J Med Chem (2005) 48 : 38 -55
PubMed 15634000 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 29 9.15 10.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL178853 1 10.10
CHEMBL178682 1 10.05
CHEMBL179539 1 10.00
CHEMBL362607 1 9.72
CHEMBL179263 1 9.72
CHEMBL178192 1 9.68
CHEMBL368699 1 9.68
CHEMBL369502 1 9.68
CHEMBL362662 1 9.66
CHEMBL179472 1 9.64
CHEMBL360885 1 9.60
CHEMBL178950 1 9.59
CHEMBL555146 1 9.57
CHEMBL361801 1 9.57
CHEMBL179372 1 9.46
CHEMBL179702 1 9.39
CHEMBL179015 1 9.36
CHEMBL351231 1 9.35
CHEMBL359462 1 9.31
CHEMBL426603 1 9.29
CHEMBL178191 1 9.28
CHEMBL178410 1 9.28
CHEMBL180368 1 9.16
CHEMBL180125 1 9.06
CHEMBL368398 1 8.67
CHEMBL14638 CIPROXIFAN 1 7.20
CHEMBL260374 THIOPERAMIDE 1 7.14
CHEMBL361355 1 7.03
CHEMBL302196 1 6.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL178853 Ki = 0.08 nM 10.10
CHEMBL178682 Ki = 0.09 nM 10.05
CHEMBL179539 Ki = 0.1 nM 10.00
CHEMBL362607 Ki = 0.19 nM 9.72
CHEMBL179263 Ki = 0.19 nM 9.72
CHEMBL178192 Ki = 0.21 nM 9.68
CHEMBL368699 Ki = 0.21 nM 9.68
CHEMBL369502 Ki = 0.21 nM 9.68
CHEMBL362662 Ki = 0.22 nM 9.66
CHEMBL179472 Ki = 0.23 nM 9.64
CHEMBL360885 Ki = 0.25 nM 9.60
CHEMBL178950 Ki = 0.26 nM 9.59
CHEMBL555146 Ki = 0.27 nM 9.57
CHEMBL361801 Ki = 0.27 nM 9.57
CHEMBL179372 Ki = 0.35 nM 9.46
CHEMBL179702 Ki = 0.41 nM 9.39
CHEMBL179015 Ki = 0.44 nM 9.36
CHEMBL351231 Ki = 0.45 nM 9.35
CHEMBL359462 Ki = 0.49 nM 9.31
CHEMBL426603 Ki = 0.51 nM 9.29
CHEMBL178191 Ki = 0.52 nM 9.28
CHEMBL178410 Ki = 0.52 nM 9.28
CHEMBL180368 Ki = 0.69 nM 9.16
CHEMBL180125 Ki = 0.88 nM 9.06
CHEMBL368398 Ki = 2.15 nM 8.67
CHEMBL14638 CIPROXIFAN Ki = 63.0 nM 7.20
CHEMBL260374 THIOPERAMIDE Ki = 72.0 nM 7.14
CHEMBL361355 Ki = 93.0 nM 7.03
CHEMBL302196 Ki = 760.0 nM 6.12