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Assay Detail

CHEMBL617263

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

Binding
Half-maximal inhibition of [3H]- Ketanserin binding to 5-hydroxytryptamine 2A receptor in rat cerebral cortex homogenate
23
Total Activities
21
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Tissue Cerebral cortex
Confidence 8 — Homologous single protein target
Curated By Expert

Target

5-hydroxytryptamine receptor 2A (CHEMBL322)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Pyrrolo[1,3]benzothiazepine-based atypical antipsychotic agents. Synthesis, structure-activity relationship, molecular modeling, and biological studies.
Campiani G, Butini S, Gemma S, Nacci V, Fattorusso C, Catalanotti B, Giorgi G, Cagnotto A, Goegan M, Mennini T, Minetti P, Di Cesare MA, Mastroianni D, Scafetta N, Galletti B, Stasi MA, Castorina M, Pacifici L, Ghirardi O, Tinti O, Carminati P.
J Med Chem (2002) 45 : 344 -359
PubMed 11784139 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 23 8.27 9.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL303313 1 9.85
CHEMBL64249 CLOROTEPINE 2.0 1 9.64
CHEMBL64875 1 9.48
CHEMBL93240 METITEPINE 2.0 1 9.40
CHEMBL120512 1 8.94
CHEMBL368324 1 8.83
CHEMBL2111781 1 8.76
CHEMBL2111783 2 8.40
CHEMBL715 OLANZAPINE 4.0 1 8.40
CHEMBL333455 1 8.36
CHEMBL118889 1 8.23
CHEMBL119687 1 8.06
CHEMBL42 CLOZAPINE 4.0 1 8.00
CHEMBL121274 1 7.92
CHEMBL2111782 2 7.74
CHEMBL116542 1 7.65
CHEMBL333955 1 7.64
CHEMBL333246 1 7.60
CHEMBL118092 1 7.27
CHEMBL118919 1 7.13
CHEMBL54 HALOPERIDOL 4.0 1 6.78

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL303313 Ki = 0.1413 nM 9.85
CHEMBL64249 CLOROTEPINE Ki = 0.2291 nM 9.64
CHEMBL64875 Ki = 0.3311 nM 9.48
CHEMBL93240 METITEPINE Ki = 0.3981 nM 9.40
CHEMBL120512 Ki = 1.148 nM 8.94
CHEMBL368324 Ki = 1.479 nM 8.83
CHEMBL2111781 Ki = 1.738 nM 8.76
CHEMBL2111783 Ki = 3.981 nM 8.40
CHEMBL715 OLANZAPINE Ki = 3.981 nM 8.40
CHEMBL2111783 Ki = 4.266 nM 8.37
CHEMBL333455 Ki = 4.365 nM 8.36
CHEMBL118889 Ki = 5.888 nM 8.23
CHEMBL119687 Ki = 8.71 nM 8.06
CHEMBL42 CLOZAPINE Ki = 10.0 nM 8.00
CHEMBL121274 Ki = 12.02 nM 7.92
CHEMBL2111782 Ki = 18.2 nM 7.74
CHEMBL2111782 Ki = 19.95 nM 7.70
CHEMBL116542 Ki = 22.39 nM 7.65
CHEMBL333955 Ki = 22.91 nM 7.64
CHEMBL333246 Ki = 25.12 nM 7.60
CHEMBL118092 Ki = 53.7 nM 7.27
CHEMBL118919 Ki = 74.13 nM 7.13
CHEMBL54 HALOPERIDOL Ki = 165.96 nM 6.78