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Assay Detail

CHEMBL827381

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

Binding
In vitro binding affinity for Dopamine receptor D2
20
Total Activities
20
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Dopamine D1/D5 receptor antagonists with improved pharmacokinetics: design, synthesis, and biological evaluation of phenol bioisosteric analogues of benzazepine D1/D5 antagonists.
Wu WL, Burnett DA, Spring R, Greenlee WJ, Smith M, Favreau L, Fawzi A, Zhang H, Lachowicz JE.
J Med Chem (2005) 48 : 680 -693
PubMed 15689153 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 20 5.69 6.63

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL369477 1 6.63
CHEMBL361179 1 6.59
CHEMBL368926 1 6.18
CHEMBL298406 ECOPIPAM 3.0 1 6.01
CHEMBL367108 1 6.01
CHEMBL62 SCH-23390 1 6.00
CHEMBL368482 1 5.99
CHEMBL177896 1 5.98
CHEMBL366347 1 5.86
CHEMBL359696 1 5.82
CHEMBL367020 1 5.54
CHEMBL179215 1 5.52
CHEMBL177267 1 5.50
CHEMBL366839 1 5.49
CHEMBL180059 1 5.45
CHEMBL366569 1 5.30
CHEMBL359605 1 5.00
CHEMBL177331 1 5.00
CHEMBL175965 1 5.00
CHEMBL424776 1 5.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL369477 Ki = 232.0 nM 6.63
CHEMBL361179 Ki = 257.0 nM 6.59
CHEMBL368926 Ki = 661.0 nM 6.18
CHEMBL298406 ECOPIPAM Ki = 980.0 nM 6.01
CHEMBL367108 Ki = 984.0 nM 6.01
CHEMBL62 SCH-23390 Ki = 1000.0 nM 6.00
CHEMBL368482 Ki = 1023.0 nM 5.99
CHEMBL177896 Ki = 1040.0 nM 5.98
CHEMBL366347 Ki = 1390.0 nM 5.86
CHEMBL359696 Ki = 1530.0 nM 5.82
CHEMBL367020 Ki = 2890.0 nM 5.54
CHEMBL179215 Ki = 3000.0 nM 5.52
CHEMBL177267 Ki = 3200.0 nM 5.50
CHEMBL366839 Ki = 3270.0 nM 5.49
CHEMBL180059 Ki = 3550.0 nM 5.45
CHEMBL366569 Ki = 5010.0 nM 5.30
CHEMBL359605 Ki = 10000.0 nM 5.00
CHEMBL177331 Ki = 10000.0 nM 5.00
CHEMBL175965 Ki = 10000.0 nM 5.00
CHEMBL424776 Ki = 10000.0 nM 5.00