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

CHEMBL876375

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

Binding
Inhibition of [3H]prazosin binding to rat Alpha-1 adrenergic receptor
15
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Adrenergic receptor alpha-1 (CHEMBL1907610)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

Discovery of new tetracyclic tetrahydrofuran derivatives as potential broad-spectrum psychotropic agents.
Fernández J, Alonso JM, Andrés JI, Cid JM, Díaz A, Iturrino L, Gil P, Megens A, Sipido VK, Trabanco AA.
J Med Chem (2005) 48 : 1709 -1712
PubMed 15771415 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 15 7.27 8.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL85 RISPERIDONE 4.0 1 8.60
CHEMBL193639 2 8.12
CHEMBL42 CLOZAPINE 4.0 1 7.66
CHEMBL363581 1 7.50
CHEMBL435301 1 7.46
CHEMBL366164 1 7.39
CHEMBL194659 1 7.15
CHEMBL6437 MIANSERIN 4.0 1 7.13
CHEMBL715 OLANZAPINE 4.0 1 7.06
CHEMBL329566 1 6.97
CHEMBL364270 1 6.64
CHEMBL193435 1 6.63
CHEMBL195706 1 6.47
CHEMBL654 MIRTAZAPINE 4.0 1 6.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL85 RISPERIDONE Ki = 2.5 nM 8.60
CHEMBL193639 Ki = 7.5 nM 8.12
CHEMBL193639 Ki = 8.8 nM 8.06
CHEMBL42 CLOZAPINE Ki = 22.0 nM 7.66
CHEMBL363581 Ki = 32.0 nM 7.50
CHEMBL435301 Ki = 35.0 nM 7.46
CHEMBL366164 Ki = 41.0 nM 7.39
CHEMBL194659 Ki = 71.0 nM 7.15
CHEMBL6437 MIANSERIN Ki = 74.0 nM 7.13
CHEMBL715 OLANZAPINE Ki = 88.0 nM 7.06
CHEMBL329566 Ki = 108.0 nM 6.97
CHEMBL364270 Ki = 228.0 nM 6.64
CHEMBL193435 Ki = 234.0 nM 6.63
CHEMBL195706 Ki = 338.0 nM 6.47
CHEMBL654 MIRTAZAPINE Ki = 608.0 nM 6.22