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Assay Detail

CHEMBL817082

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

Binding
Inhibition constant for vasopressin-stimulated adenylate cyclase of medullary membranes of human kidney
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Vasopressin V2 receptor (CHEMBL1790)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-activity relationships of novel vasopressin antagonists containing C-terminal diaminoalkanes and (aminoalkyl)guanidines.
Callahan JF, Ashton-Shue D, Bryan HG, Bryan WM, Heckman GD, Kinter LB, McDonald JE, Moore ML, Schmidt DB, Silvestri JS.
J Med Chem (1989) 32 : 391 -396
PubMed 2521519 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 8.36 8.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL416114 1 8.48
CHEMBL2370646 1 8.44
CHEMBL265591 1 8.43
CHEMBL2370640 1 8.38
CHEMBL2370642 1 8.32
CHEMBL2370641 1 8.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL416114 Ki = 3.3 nM 8.48
CHEMBL2370646 Ki = 3.6 nM 8.44
CHEMBL265591 Ki = 3.7 nM 8.43
CHEMBL2370640 Ki = 4.2 nM 8.38
CHEMBL2370642 Ki = 4.8 nM 8.32
CHEMBL2370641 Ki = 7.6 nM 8.12