GPCR19
GPCR19, également connu sous le nom de GPR19, est un membre de la famille des récepteurs couplés aux protéines G dont les rôles sont encore en cours d'élucidation dans divers processus physiologiques. Bien que moins caractérisé que d'autres GPCR, GPCR19 suscite un intérêt particulier dans les recherches visant à découvrir de nouvelles cibles thérapeutiques pour les maladies métaboliques, le cancer et les troubles neurologiques. Chez CymitQuimica, nous offrons une sélection d'outils de recherche et de réactifs pour soutenir vos investigations sur les fonctions et les applications thérapeutiques potentielles de GPCR19.
31 produits trouvés pour "GPCR19"
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Hyodeoxycholic acid
CAS :<p>Hyodeoxycholic acid (NSC 60672) has been used in trials studying the treatment of Hypercholesterolemia.</p>Formule :C24H40O4Degré de pureté :97.29% - 98.82%Couleur et forme :SolidMasse moléculaire :392.57Deoxycholic acid
CAS :<p>Deoxycholic acid (Cholanoic Acid) is a bile acid formed by bacterial action from cholate.</p>Formule :C24H40O4Degré de pureté :99.91% - 99.91%Couleur et forme :Crystals From Alc SolidMasse moléculaire :392.57Ursodeoxycholic acid
CAS :<p>Ursodeoxycholic acid (UDCA) is a potent inhibitor of liver-specific fatty acid transporter 5 (FATP5),inhibits cholesterol absorption. High-Quality, Low-Cost!</p>Formule :C24H40O4Degré de pureté :99.74% - ≥95%Couleur et forme :White - Almost White Solid PowderMasse moléculaire :392.57PEN (rat)
CAS :<p>PEN (rat) is an Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.</p>Formule :C102H169N27O33Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :2301.62TGR5 agonist 1
<p>Compound 18 (TGR5 agonist 1) is a potent agonist of TGR5, exhibiting an EC50 value of 0.31 µM [1].</p>Formule :C28H48NNaO6SCouleur et forme :SolidMasse moléculaire :549.74TGR5 agonist 4
<p>TGR5 agonist 4 (compound 19), a derivative of cholic acid, selectively activates the TGR5 receptor with an effective concentration (EC50) of 4 μM [1].</p>Formule :C24H38F2O5Couleur et forme :SolidMasse moléculaire :444.555-HT7R antagonist 1 free base
CAS :<p>5-HT7R antagonist 1 (free base) is a G protein-biased antagonist for the 5-HT 7 R receptor, with a dissociation constant (K i) of 6.5 nM.</p>Formule :C14H17ClN4Couleur et forme :SolidMasse moléculaire :276.77PEN (human)
CAS :<p>PEN (human) is an Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.</p>Formule :C97H159N27O32Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :2215.49Cholic Acid 7-sulfate
CAS :<p>Cholic acid 7-sulfate: a cholic acid metabolite with added sulfate at position 7, increased in feces of male mice with specific diets.</p>Formule :C24H40O8SCouleur et forme :SolidMasse moléculaire :488.64TGR5 agonist 2
<p>TGR5 agonist 2 (compound 19) serves as a highly potent agonist of TGR5, demonstrating an EC50 value of 0.27 µM [1].</p>Formule :C29H50NNaO6SCouleur et forme :SolidMasse moléculaire :563.77TGR5 agonist 6
CAS :<p>Compound 22b, also known as TGR5 agonist 6, is a non-systemic, intestine-targeted TGR5 agonist that demonstrates significant and sustained blood glucose-lowering effects with an acceptable safety profile.</p>Formule :C42H48Cl2N6O6Couleur et forme :SolidMasse moléculaire :803.77TGR5 agonist 7
<p>TGR5 agonist 7 (Compound 22-Na) is an intestine-restricted, orally active agonist of the G protein-coupled bile acid receptor TGR5 (GPBAR1 or GPR131) with an EC50 of less than 1 μM. In mouse models, it demonstrates blood glucose-lowering effects, making it useful for diabetes research.</p>Formule :C37H59N2NaO9SCouleur et forme :SolidMasse moléculaire :730.93Triamterene
CAS :<p>Triamterene is a barosensitive epithelial sodium channel (ENaC) blocker with a diuretic effect. It can also act as an inhibitor of the TGR5 receptor, reducing GLP-1 secretion and cAMP level increases induced by TGR5 activation in a dose-dependent manner.</p>Formule :C12H11N7Degré de pureté :99.77%Couleur et forme :Yellow Yellow SolidMasse moléculaire :253.26BAR502
CAS :<p>BAR502 is a dual GPBAR1 and FXR agonist (IC50s: 0.4 μM and 2 μM).</p>Formule :C25H44O3Degré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :392.62BAR501
CAS :<p>BAR501是高效选择性的 GPBAR1激动剂(EC50:1 μM)。</p>Formule :C26H46O3Degré de pureté :99.29% - 99.68%Couleur et forme :SolidMasse moléculaire :406.64TC-G 1005
CAS :<p>TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5).</p>Formule :C25H25N3O2Degré de pureté :98.60% - 99.78%Couleur et forme :SolidMasse moléculaire :399.48Deoxycholic acid sodium salt
CAS :<p>Deoxycholic acid sodium salt (Sodium deoxycholate) can activate the G protein-coupled bile acid receptor TGR5 that stimulates BAT thermogenic activity.</p>Formule :C24H39NaO4Degré de pureté :97.88% - 99.75%Couleur et forme :Cream Crystalline PowderMasse moléculaire :414.56SBI-115
CAS :<p>SBI-115 is an antagonist of TGR5. SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5</p>Formule :C14H13ClN2O4SDegré de pureté :99.53% - 99.78%Couleur et forme :SolidMasse moléculaire :340.78TGR5 Receptor Agonist
CAS :<p>TGR5 is a potent TGR5(GPCR19) agonist.</p>Formule :C18H14Cl2N2O2Degré de pureté :99.77% - ≥95%Couleur et forme :SolidMasse moléculaire :361.22PEN (human) aceate
<p>PEN (human) aceate, one of the most abundant hypothalamic neuropeptide and derived from the proprotein ProSAAS, is an endogenous ligand of GPR83.</p>Formule :C99H163N27O34Degré de pureté :99.25%Couleur et forme :SolidMasse moléculaire :2275.51SB756050
CAS :<p>SB756050 is a specific TGR5 agonist.</p>Formule :C21H28N2O8S2Degré de pureté :98.78% - >99.99%Couleur et forme :SolidMasse moléculaire :500.59Ursodeoxycholic acid sodium
CAS :<p>Ursodeoxycholic acid sodium (Sodium Ursodeoxycholate) is a naturally occurring secondary bile acid with anti-inflammatory and cytoprotective activities.</p>Formule :C24H40NaO4Degré de pureté :99.66% - 99.96%Couleur et forme :SolidMasse moléculaire :415.56CAY10789
CAS :<p>CAY10789: potent CysLT1R antagonist (IC50 2.8 µM), GPBAR1 agonist (EC50 3 µM), reduces U937 cell adhesion, TNF-α, stable with promising pharmacokinetics.</p>Formule :C17H15NO2Couleur et forme :SolidMasse moléculaire :265.31WB403
CAS :<p>WB403 activates TGR5, lowers fasting/postprandial glucose and HbA1c, enhances glucose tolerance, and normalizes pancreatic α/β-cells in diabetic mice.</p>Formule :C19H19BrN2OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :403.34TGR5 agonist 3
CAS :<p>Compound 8, a cholic acid derivative, functions as a selective TGR5 agonist and exhibits an EC50 value of 5 μM [1].</p>Formule :C28H48O5Couleur et forme :SolidMasse moléculaire :464.68INT-777 R-enantiomer
CAS :<p>INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5.</p>Formule :C27H46O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :450.65RO5527239
CAS :<p>RO5527239 is a potent, orally available GPBAR1 agonist agent.</p>Formule :C28H31N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :457.56INT-777
CAS :<p>INT-777 (S-EMCA) is a potent TGR5 agonist with an EC50 of 0.82 μM.</p>Formule :C27H46O5Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :450.655-HT7R antagonist 1
<p>5-HT7R antagonist 1 is a G protein-biased antagonist with Ki of 6.5 nM for 5-HT 7R.</p>Formule :C14H18Cl2N4Couleur et forme :SolidMasse moléculaire :313.23TGR5 Receptor Agonist 3
CAS :<p>TGR5 Receptor Agonist 3 is a GPBAR1 agonist with EC50 of 16.4 nM (hTGR5) & 209 nM (mTGR5), ensures gallbladder safety and reduces filling.</p>Formule :C29H27N3O6Couleur et forme :SolidMasse moléculaire :513.54GPBAR1-IN-3
CAS :<p>GPBAR1-IN-3 (Compound 14) is both a selective agonist for GPBAR1, with an EC50 value of 0.17 μM, and an antagonist for CysLT1R [1].</p>Formule :C21H23NO2Couleur et forme :SolidMasse moléculaire :321.41
