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

CHEMBL828254

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

Binding
Binding affinity against 5-Hydroxy tryptamine 7 receptor
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

5-hydroxytryptamine receptor 7 (CHEMBL3155)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Aminotriazine 5-HT7 antagonists.
Mattson RJ, Denhart DJ, Catt JD, Dee MF, Deskus JA, Ditta JL, Epperson J, Dalton King H, Gao A, Poss MA, Purandare A, Tortolani D, Zhao Y, Yang H, Yeola S, Palmer J, Torrente J, Stark A, Johnson G.
Bioorg Med Chem Lett (2004) 14 : 4245 -4248
PubMed 15261279 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 8.09 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL413049 1 8.70
CHEMBL182937 1 8.70
CHEMBL180086 1 8.70
CHEMBL182174 1 8.52
CHEMBL183862 1 8.52
CHEMBL182322 1 8.30
CHEMBL183462 1 8.10
CHEMBL182797 1 8.10
CHEMBL182418 1 8.05
CHEMBL441312 1 8.00
CHEMBL182840 1 7.64
CHEMBL180946 1 7.44
CHEMBL182805 1 7.27
CHEMBL182121 1 7.22
CHEMBL360374 1 -
CHEMBL183347 1 -
CHEMBL185560 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL413049 Ki = 2.0 nM 8.70
CHEMBL182937 Ki = 2.0 nM 8.70
CHEMBL180086 Ki = 2.0 nM 8.70
CHEMBL182174 Ki = 3.0 nM 8.52
CHEMBL183862 Ki = 3.0 nM 8.52
CHEMBL182322 Ki = 5.0 nM 8.30
CHEMBL183462 Ki = 8.0 nM 8.10
CHEMBL182797 Ki = 8.0 nM 8.10
CHEMBL182418 Ki = 9.0 nM 8.05
CHEMBL441312 Ki = 10.0 nM 8.00
CHEMBL182840 Ki = 23.0 nM 7.64
CHEMBL180946 Ki = 36.0 nM 7.44
CHEMBL182805 Ki = 54.0 nM 7.27
CHEMBL182121 Ki = 60.0 nM 7.22
CHEMBL360374 Ki > 1000.0 nM -
CHEMBL183347 Ki > 41000.0 nM -
CHEMBL185560 Ki > 1000.0 nM -