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Assay Detail

CHEMBL820893

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

Binding
Inhibition of radioligand [3H]AVP binding to V1 receptor in rat liver plasma membrane
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Tissue Liver
Subcellular Plasma Membrane
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Vasopressin V1 receptor (CHEMBL2095221)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

Enhanced selectivity of oxytocin antagonists containing sarcosine in position 7.
Pavo I, Slaninova J, Klein U, Fahrenholz F.
J Med Chem (1994) 37 : 255 -259
PubMed 7507528 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 12 8.69 9.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL384292 1 9.66
CHEMBL438387 1 9.49
CHEMBL265264 1 9.23
CHEMBL411420 1 9.21
CHEMBL373742 VASOPRESSIN 4.0 1 9.19
CHEMBL265017 1 9.02
CHEMBL330022 1 8.70
CHEMBL274397 1 8.42
CHEMBL414582 1 8.08
CHEMBL1793955 1 8.08
CHEMBL415230 1 7.88
CHEMBL87636 1 7.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL384292 Kd = 0.22 nM 9.66
CHEMBL438387 Kd = 0.32 nM 9.49
CHEMBL265264 Kd = 0.59 nM 9.23
CHEMBL411420 Kd = 0.62 nM 9.21
CHEMBL373742 VASOPRESSIN Kd = 0.65 nM 9.19
CHEMBL265017 Kd = 0.96 nM 9.02
CHEMBL330022 Kd = 2.0 nM 8.70
CHEMBL274397 Kd = 3.8 nM 8.42
CHEMBL414582 Kd = 8.28 nM 8.08
CHEMBL1793955 Kd = 8.28 nM 8.08
CHEMBL415230 Kd = 13.1 nM 7.88
CHEMBL87636 Kd = 50.1 nM 7.30