Examples of using Agonists in English and their translations into Urdu
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Ecclesiastic
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Colloquial
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Computer
Previous Agonists- what are they?
Drug Class serotonin receptor agonists.
The effect of GABA agonists are increased by ivermectin.
URB 597 enhanced the behavioural effects of anandamide butnot other CB1 agonists.
GnRH agonists that are mainly used or solely in medicine embodydeslorelin and fertirelin.
People also translate
Lorcaserin is in a class of medications called serotonin receptor agonists.
Dopamine agonists(such as cabergoline, bromocriptine and quinagolide) can be taken as tablets.
Obeticholic Acid powder is in a class of medications called farnesoid X receptor agonists.
GnRH agonists may be administered by injection, by an implant, or intranasally as a nasal spray.
Lorcaserin hydrochloride is a rawmaterial belonging to the class of serotonin receptor agonists.
GnRH agonists are given by injections into fat, as implants placed into fat, and as nasal sprays.
Raw Lorcaserin powder belongs to aclass of drugs known as serotonin receptor agonists.
Also Semaglutide research shows that GLP-1 agonists has a lower stroke risk compared to other controls.
Serotonin agonists are used as antidepressants, anxiolytics, and in the treatment of migraine disorders.
Raw Palmitoylethanolamide powder(PEA) is an endogenous fatty acid amide,belonging to the class of nuclear factor agonists.
Semaglutide is a glucagon-like peptide-1 receptor agonists which people also refer to them as GLP-1 agonists.
GnRH agonists that are marketed and are offered for medical use embody buserelin, Gonadorelin, goserelin, histrelin, leuprorelin, nafarelin, and triptorelin.
Except for Gonadorelin, that is employed as a Progonadotropin,and all approved GnRH agonists are used as anti-gonadotropins.
Position statement on the use of dopamine agonists in endocrine disorders; Society for Endocrinology(Feb 2009- reviewed Nov 2011).
With the exception of gonadorelin, which is used as a progonadotropin,all approved GnRH agonists are used as antigonadotropins.
Studies done in the early 2000s have found that GW 501516 andother PPAR agonists have also been able to stop metabolic disorders such as obesity and diabetes through specific gene expressions.
GnRH agonists are synthetically shapely when the natural GnRH decapeptide with specific modifications, sometimes double and single substitutions and usually in position vi(amino acid substitution), nine(alkylation) and ten(deletion).
Preliminary data from several clinical studies indicate that compared to LHRH agonists, Degarelix was linked to considerably higher overall survival within the 1st year of treatment.
In vivo: When administered to mice at 16 mg/kg, intraperitoneally, JZL-184 reduces MAGL activity by 85%, elevates brain 2-AG levels by 8-fold, and elicits analgesic activity in a variety of pain assays thatqualitatively mimics direct central cannabinoid(CB1) agonists.
Studies conducted in the early 21st century have found that GW501516 andother PPAR agonists can also prevent metabolic disorders such as obesity and diabetes through specific gene expression.
When administered to mice at 16 mg/kg, intraperitoneally, JZL-184 reduces MAGL activity by 85%, elevates brain 2-AG levels by 8-fold, and elicits analgesic activity in a variety of pain assays thatqualitatively mimics direct central cannabinoid(CB1) agonists.
Racetam class nootropics like piracetam are considered acetylcholine agonists, compounds that increase the production and release of acetylcholine by stimulating the appropriate neurotransmitter receptor sites.
Lorcaserin HCL powder is a selective 5-HT2C receptor agonist that is thought to decrease food intake through the central POMC system.
Flibanserin is in aclass of medications called a serotonin receptor 1A agonist/serotonin receptor 2A antagonist.
Raw Palmitoylethanolamide powder Application Raw Palmitoylethanolamide powder is an endogenous CB2 cannabinoid receptor agonist and selective GPR55 agonist.