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34 results about "Vasopressin receptor" patented technology

The actions of vasopressin are mediated by stimulation of tissue-specific G protein-coupled receptors (GPCRs) called vasopressin receptors that are classified into the V₁ (V1A), V₂, and V₃ (V1B) receptor subtypes. These three subtypes differ in localization, function and signal transduction mechanisms.

Vasopressin pathway polymorphisms as indicators of subject outcome in critically ill subjects

The invention provides methods, nucleic acids, compositions and kits for predicting a subject's response to treatment with one or more vasopressin receptor agonists to identify subjects having a greater benefit from treatment with vasopressin receptor agonist(s). The method generally comprises determining a vasopressin pathway associated gene polymorphism genotype(s) of a subject for one or more polymorphisms in the these genes, comparing the determined genotype with known genotypes for the polymorphism that correspond with an improved response genotype to identify potential subjects having an inflammatory condition who are more likely to benefit from treatment with a vasopressin receptor agonist and subsequent to treatment recover from the inflammatory condition. The invention also provides for methods of treating such subjects with vasopressin receptor agonists based on the subject's genotype.
Owner:THE UNIV OF BRITISH COLUMBIA +1

Triazoles as oxytocin antagonists

The present invention relates to triazole derivatives of formula (I) notably for use as pharmaceutically active compounds, as well as pharmaceutical formulations containing such triazole derivatives. Said triazoles are useful in the treatment and / or prevention of preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. In particular, the present invention is related to triazole derivatives displaying a substantial modulatory, in particular antagonistic activity, of the oxytocin and / or vasopressin receptor. More preferably, said compounds are useful in the treatment and / or prevention of disease states mediated by oxytocin and / or vasopressin. The present invention is furthermore related to novel triazole derivatives as well as to methods of their preparation.
Owner:MERCK SERONO SA

Pharmaceutically active sulfanilide derivatives

The present invention relates to sulfanilide derivatives of formula (I), in which R1 and R2 are optionally substituted aryl and heteroaryl groups and the other variables are as defined in the claims, for use as pharmaceutically active compounds, as well as pharmaceutical formulations containing such sulfanilide derivatives. Said derivatives are useful in the treatment and / or prevention of preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. In particular, the present invention is related to sulfanilide derivatives displaying a substantial modulatory, in particular antagonistic activity, of the oxytocin and / or vasopressin receptor. More preferably, said compounds are useful in the treatment and / or prevention of disease states mediated by oxytocin and / or vasopressin, including preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. The present invention is furthermore related to novel sulfanilide derivatives as well as to methods of their preparation.
Owner:MERCK SERONO SA

V1b receptor antagonist for use in the treatment of patients having an elevated avp level and/or an elevated copeptin level

The present invention relates to a vasopressin receptor 1B (V1B) antagonist for use in the treatment of depressive symptoms and / or anxiety symptoms in patients showing an elevated arginine vasopressin (AVP) level and / or an elevated copeptin level. The present invention further relates to a method for predicting the treatment response to a V1B antagonist in patients with depressive symptoms and / or anxiety symptoms.
Owner:MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN EV

Peptides and pharmaceutical compositions for use in the treatment by nasal administration of patients suffering from anxiety and sleep disorders

InactiveUS20140249090A1Increase alertnessNervous disorderPeptide/protein ingredientsPanicGeneralised anxiety disorder
The present invention provides peptides for use in a medicament which is administered nasally, wherein the peptide is an agonist of neuropeptide S receptor (NPSR), of the receptor TGR23 and/or of vasopressin receptor-related receptor 1 (VRR1) or for use in the treatment of a patient by causing, promoting or increasing relieve or healing of phobic anxiety, avoidance anxiety, dissociative anxiety such as flashbacks, depersonalization, derealization, intrusions, vegetative symptoms related to anxiety symptoms, especially in panic attacks, in posttraumatic stress disorder, in generalised anxiety disorder and in anxiety accompanying depressive, or psychotic episodes, arousal, awakening, alertness, activity, spontaneous movement, an anxiolytic effect or a combination thereof in the patient, wherein the peptide is administered nasally or for use in the prophylaxis and/or treatment of an anxiety or sleep disorder, especially in any type of hypersomnia like idiopathic hypersomnia, wherein the peptide is administered nasally. Further provided are pharmaceutical compositions for nasal administration comprising at least one of said peptides, uses of said peptide or said pharmaceutical composition. The invention also provides a method for identifying target neurons of a peptide in an animal, wherein the peptide is administered nasally.
Owner:MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN EV

Method for stabilizing blood pressure in hemodialysis subjects

InactiveUS20070213259A1Reduce excessFacilitate reducing excess extracellular fluidBiocideOrganic active ingredientsHemodialysisHaemodialysis machine
The present invention provides a method for regulating blood pressure in a hemodialysis subject using a vasopressin receptor agonist, so as to facilitate removal of excessive extracellular fluid in the subject.
Owner:INTRADIALYTIC PHARMA

Compound with function of diuresis, preparation method and functions thereof

InactiveCN102690259AImprove solubilitySolve problems such as poor absorptionNervous disorderOrganic chemistryDiuresisSympathetic nervous system
The invention belongs to the technical field of medicaments with a function of diuresis, and discloses benzazepine compound with a general formula I structure, pharmaceutically acceptable salts, an R definition and R claims. The invention further discloses a preparation method for the compound, a medicament composition which takes the compound or the pharmaceutically acceptable salts as active effective components and functions of preventing or treating illnesses related to an arginine vasopressin receptor V1a, an arginine vasopressin receptor V1b, an arginine vasopressin receptor V2, a sympathetic nervous system or a system of rennin-angiotensin-aldosterone.
Owner:TIANJIN INSTITUTE OF PHARMA RESEARCH

Label-free arginine vasopressin receptor cell model construction and ligand screening method

The invention relates to a label-free arginine vasopressin receptor cell model construction and ligand screening method, in particular to a method for building the models of a subtype (V1a receptor) of an arginine vasopressin receptor on different cell lines and for carrying ligand screening by using a label-free cell dynamic mass reset technology. The V1a receptor model disclosed by the invention is constructed on an HEK293 cell line for endogenous expression of the V1a receptor and a transfected CHO-V1a cell line. The method has the characteristics of being close to an in-vivo real environment, free of labels, capable of monitoring in real time, high in flux and simple to operate, and ligands with V1a receptor activity, including agonists and antagonists, can be screened.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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