Page last updated: 2024-08-05 15:40:19

vasopressin receptor antagonist

Any drug which blocks vasopressin receptors.

ChEBI ID: 59680

Members (2)

MemberDefinitionClass
conivaptanThe amide resulting from the formal condensation of 4-[(biphenyl-2-ylcarbonyl)amino]benzoic acid with the benzazepine nitrogen of 2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine. It is an antagonist for two of the three types of arginine vasopressin (AVP) receptors, V1a and V2. It is used as its hydrochloride salt for the treatment of hyponatraemia (low blood sodium levels) caused by syndrome of inappropriate antidiuretic hormone (SIADH).conivaptan
tolvaptanA benzazepine derivative incorporating a benzenedicarboxamide function whch is a selective vasopressin V2 receptor antagonist used to treat euvolemic and hypervolemic hyponatremia. It is also used in the treatment of rapidly progressing autosomal dominant polycystic kidney disease to slow the rate of cyst development and renal insufficiency. Tolvaptan is a racemate consisting of a 1:1 mixture of 5R and 5S stereomers.tolvaptan

Research

Studies (1,039)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-19900 (0.00)18.7374
1990's15 (1.44)18.2507
2000's163 (15.69)29.6817
2010's613 (59.00)24.3611
2020's248 (23.87)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials189 (16.36%)5.53%
Reviews271 (23.46%)6.00%
Case Studies110 (9.52%)4.05%
Observational48 (4.16%)0.25%
Other537 (46.49%)84.16%

Protein Targets (33)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
AR proteinHomo sapiens (human)Potency23.914522
cytochrome P450 2C9, partialHomo sapiens (human)Potency27.540411
cytochrome P450 2D6Homo sapiens (human)Potency12.134812
cytochrome P450 family 3 subfamily A polypeptide 4Homo sapiens (human)Potency3.609412
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency29.849311
estrogen nuclear receptor alphaHomo sapiens (human)Potency23.914522
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency26.603211
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency28.433433
EWS/FLI fusion proteinHomo sapiens (human)Potency24.816133
GVesicular stomatitis virusPotency27.540411
GLI family zinc finger 3Homo sapiens (human)Potency18.833611
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency11.985611
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency27.540411
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency27.540412
Interferon betaHomo sapiens (human)Potency27.540411
LuciferasePhotinus pyralis (common eastern firefly)Potency29.798122
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency33.488911
progesterone receptorHomo sapiens (human)Potency21.131711
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency32.554822
retinoid X nuclear receptor alphaHomo sapiens (human)Potency26.832522
Spike glycoproteinSevere acute respiratory syndrome-related coronavirusPotency31.099012
TDP1 proteinHomo sapiens (human)Potency21.136022
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency25.156622
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency0.016911
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency3.790211

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
ATP-binding cassette sub-family C member 3Homo sapiens (human)IC50133.000011
Bile salt export pumpHomo sapiens (human)IC509.990011
Canalicular multispecific organic anion transporter 1Homo sapiens (human)IC50133.000011
Multidrug resistance-associated protein 4Homo sapiens (human)IC50133.000011
Oxytocin receptorRattus norvegicus (Norway rat)Ki10.000011
Vasopressin V1a receptorHomo sapiens (human)IC500.264034
Vasopressin V1a receptorHomo sapiens (human)Ki0.109533
Vasopressin V1b receptorRattus norvegicus (Norway rat)Ki10.000011
Vasopressin V2 receptorHomo sapiens (human)IC500.121045
Vasopressin V2 receptorHomo sapiens (human)Ki0.001255