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

CHEMBL3875676

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

Binding
Displacement of [3H]spiperone from dopamine D2 receptor in Sprague-Dawley rat striatum incubated for 30 mins by liquid scintillation counting analysis
42
Total Activities
42
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

Target

D(2) dopamine receptor (CHEMBL339)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Synthesis and biological evaluation of new 6-hydroxypyridazinone benzisoxazoles: Potential multi-receptor-targeting atypical antipsychotics.
Cao X, Chen Y, Zhang Y, Qiu Y, Yu M, Xu X, Liu X, Liu BF, Zhang G.
Eur J Med Chem (2016) 124 : 713 -728
PubMed 27639363 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 42 7.22 9.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3885471 1 9.70
CHEMBL3885254 1 9.40
CHEMBL3883955 1 9.30
CHEMBL3884161 1 8.57
CHEMBL85 RISPERIDONE 4.0 1 8.43
CHEMBL3884325 1 8.21
CHEMBL3884918 1 8.11
CHEMBL3884874 1 7.97
CHEMBL3884183 1 7.79
CHEMBL3884138 1 7.57
CHEMBL3883408 1 7.55
CHEMBL3883603 1 7.48
CHEMBL3884994 1 7.45
CHEMBL3883388 1 7.42
CHEMBL3884034 1 7.42
CHEMBL3884681 1 7.42
CHEMBL3884066 1 7.42
CHEMBL3884300 1 7.39
CHEMBL3883511 1 7.39
CHEMBL3884065 1 7.38
CHEMBL3883942 1 7.36
CHEMBL3884105 1 7.34
CHEMBL3883557 1 7.34
CHEMBL3884733 1 6.76
CHEMBL3885003 1 6.75
CHEMBL3884820 1 6.42
CHEMBL3885088 1 6.30
CHEMBL3883773 1 6.28
CHEMBL3885016 1 6.22
CHEMBL3884545 1 6.19

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3885471 Ki = 0.2 nM 9.70
CHEMBL3885254 Ki = 0.4 nM 9.40
CHEMBL3883955 Ki = 0.5 nM 9.30
CHEMBL3884161 Ki = 2.7 nM 8.57
CHEMBL85 RISPERIDONE Ki = 3.7 nM 8.43
CHEMBL3884325 Ki = 6.1 nM 8.21
CHEMBL3884918 Ki = 7.8 nM 8.11
CHEMBL3884874 Ki = 10.8 nM 7.97
CHEMBL3884183 Ki = 16.2 nM 7.79
CHEMBL3884138 Ki = 26.7 nM 7.57
CHEMBL3883408 Ki = 28.1 nM 7.55
CHEMBL3883603 Ki = 33.1 nM 7.48
CHEMBL3884994 Ki = 35.4 nM 7.45
CHEMBL3884066 Ki = 38.1 nM 7.42
CHEMBL3884681 Ki = 38.5 nM 7.42
CHEMBL3883388 Ki = 38.3 nM 7.42
CHEMBL3884034 Ki = 38.5 nM 7.42
CHEMBL3884300 Ki = 41.1 nM 7.39
CHEMBL3883511 Ki = 40.3 nM 7.39
CHEMBL3884065 Ki = 41.8 nM 7.38
CHEMBL3883942 Ki = 43.7 nM 7.36
CHEMBL3884105 Ki = 45.5 nM 7.34
CHEMBL3883557 Ki = 45.3 nM 7.34
CHEMBL3884733 Ki = 174.0 nM 6.76
CHEMBL3885003 Ki = 179.0 nM 6.75
CHEMBL3884820 Ki = 379.0 nM 6.42
CHEMBL3885088 Ki = 499.0 nM 6.30
CHEMBL3883773 Ki = 524.0 nM 6.28
CHEMBL3885016 Ki = 595.0 nM 6.22
CHEMBL3884545 Ki = 648.0 nM 6.19
CHEMBL3885327 Ki = 777.0 nM 6.11
CHEMBL3884885 Ki = 808.0 nM 6.09
CHEMBL3884619 Ki = 845.0 nM 6.07
CHEMBL3885211 Ki = 916.0 nM 6.04
CHEMBL3883960 Ki = 914.0 nM 6.04
CHEMBL3883495 Ki = 953.0 nM 6.02
CHEMBL3884209 Ki = 1196.0 nM 5.92
CHEMBL3885180 Ki = 1322.0 nM 5.88
CHEMBL3883429 Ki > 10000.0 nM -
CHEMBL3884581 Ki > 10000.0 nM -
CHEMBL3885152 Ki > 10000.0 nM -
CHEMBL3883484 Ki > 10000.0 nM -