GPCR19
GPCR19, também conhecido como GPR19, é um membro da família dos receptores acoplados à proteína G, com funções que ainda estão sendo elucidadas em vários processos fisiológicos. Embora menos caracterizado do que outros GPCRs, o GPCR19 é de interesse em pesquisas focadas na descoberta de novos alvos terapêuticos para doenças metabólicas, câncer e distúrbios neurológicos. Na CymitQuimica, oferecemos uma seleção de ferramentas de pesquisa e reagentes para apoiar suas investigações sobre as funções e potenciais aplicações terapêuticas do GPCR19.
Foram encontrados 38 produtos para "GPCR19".
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Deoxycholic acid
CAS:Deoxycholic acid (Cholanoic Acid) is a bile acid formed by bacterial action from cholate.Fórmula:C24H40O4Pureza:99.84% - 99.91%Cor e Forma:SolidPeso molecular:392.57Hyodeoxycholic acid
CAS:Hyodeoxycholic acid (NSC 60672) has been used in trials studying the treatment of Hypercholesterolemia.Fórmula:C24H40O4Pureza:97.29% - 98.82%Cor e Forma:SolidPeso molecular:392.57Ursodeoxycholic acid
CAS:Ursodeoxycholic acid (UDCA) is a potent inhibitor of liver-specific fatty acid transporter 5 (FATP5),inhibits cholesterol absorption. High-Quality, Low-Cost!Fórmula:C24H40O4Pureza:99.48% - ≥95%Cor e Forma:White SolidPeso molecular:392.57GPBAR-A
CAS:GPBAR-A is a synthetic small-molecule agonist of GPBAR1, also known as TGR5, that activates this G protein–coupled bile acid receptor involved in energy homeostasis, glucose metabolism, and immune regulation, GPBAR-A is extensively studied for its therapeutic potential in metabolic disorders such as type 2 diabetes, obesity, and inflammation-related diseases.Fórmula:C23H15F7N2O2Pureza:99.99%Cor e Forma:White SolidPeso molecular:484.37TGR5 agonist 1
Compound 18 (TGR5 agonist 1) is a potent agonist of TGR5, exhibiting an EC50 value of 0.31 µM [1].Fórmula:C28H48NNaO6SCor e Forma:SolidPeso molecular:549.74TGR5 agonist 4
TGR5 agonist 4 (compound 19), a derivative of cholic acid, selectively activates the TGR5 receptor with an effective concentration (EC50) of 4 μM [1].Fórmula:C24H38F2O5Cor e Forma:SolidPeso molecular:444.555-HT7R antagonist 1 free base
CAS: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.Fórmula:C14H17ClN4Cor e Forma:SolidPeso molecular:276.77PEN (human)
CAS:PEN (human) is an Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.Fórmula:C97H159N27O32Pureza:98%Cor e Forma:SolidPeso molecular:2215.49PEN (rat)
CAS:PEN (rat) is an Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.Fórmula:C102H169N27O33Pureza:98%Cor e Forma:SolidPeso molecular:2301.62TGR5 agonist 2
TGR5 agonist 2 (compound 19) serves as a highly potent agonist of TGR5, demonstrating an EC50 value of 0.27 µM [1].Fórmula:C29H50NNaO6SCor e Forma:SolidPeso molecular:563.77TGR5 agonist 6
CAS: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.Fórmula:C42H48Cl2N6O6Cor e Forma:SolidPeso molecular:803.77TGR5 agonist 7
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.Fórmula:C37H59N2NaO9SCor e Forma:SolidPeso molecular:730.93Neuromedin S (human)
CAS:Neuromedin S (human) is a 33-amino acid neuropeptide identified as an endogenous ligand for the orphan G-protein coupled receptor (GPCR) FM-4/TGR-1, acting onCor e Forma:SolidTriamterene
CAS: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.Fórmula:C12H11N7Pureza:99.77%Cor e Forma:Yellow SolidPeso molecular:253.26LIFR/GPBAR1 modulator 1
LIFR/GPBAR1 modulator 1 is an orally active, potent GPBAR1 agonist (EC50= 0.2 μM) and LIFR inhibitor (IC50= 7.9 μM). It enhances the expression of leukemia inhibitory factor (LIF)-mediated LIFR and GPBAR1 mRNA, while significantly reducing the expression of fibrosis markers (COL1A1, ASMA, and TGFβ), decreasing TIMP1 levels, and increasing MMP9 expression. LIFR/GPBAR1 modulator 1 is applicable for research into human fibrotic diseases.Triamterene (Standard)
CAS:Triamterene (Standard) is the standard substance of Triamterene, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. 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.Fórmula:C12H11N7Cor e Forma:SolidPeso molecular:253.26PEN (human) aceate
PEN (human) aceate, one of the most abundant hypothalamic neuropeptide and derived from the proprotein ProSAAS, is an endogenous ligand of GPR83.Fórmula:C99H163N27O34Pureza:95.98%Cor e Forma:SolidPeso molecular:2275.51TC-G 1005
CAS:TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5).Fórmula:C25H25N3O2Pureza:98.60% - 99.78%Cor e Forma:SolidPeso molecular:399.48Ref: TM-T8818
1mg34,00€2mg43,00€5mg65,00€1mL*10mM (DMSO)72,00€10mg90,00€25mg178,00€50mg269,00€100mg400,00€SBI-115
CAS:SBI-115 is an antagonist of TGR5. SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5Fórmula:C14H13ClN2O4SPureza:99.53% - 99.78%Cor e Forma:SolidPeso molecular:340.78SB756050
CAS:SB756050 is a specific TGR5 agonist.Fórmula:C21H28N2O8S2Pureza:98.78% - >99.99%Cor e Forma:SolidPeso molecular:500.59
