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Application of 805250-17-3, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 805250-17-3, molcular formula is C11H12O4, introducing its new discovery.

The G protein-coupled receptor 40 (GPR40)/free fatty acid receptor 1 (FFA1) has emerged as an attractive target for a novel insulin secretagogue with glucose dependency. We previously identified phenylpropanoic acid derivative 1 (3-{4-[(2?,6?-dimethylbiphenyl-3-yl)methoxy]-2-fluorophenyl} propanoic acid) as a potent and orally available GPR40/FFA1 agonist; however, 1 exhibited high clearance and low oral bioavailability, which was likely due to its susceptibility to beta-oxidation at the phenylpropanoic acid moiety. To identify long-acting compounds, we attempted to block the metabolically labile sites at the phenylpropanoic acid moiety by introducing a fused-ring structure. Various fused-ring alkanoic acids with potent GPR40/FFA1 activities and good PK profiles were produced. Further optimizations of the lipophilic portion and the acidic moiety led to the discovery of dihydrobenzofuran derivative 53 ((6-{[4?-(2-ethoxyethoxy)-2?,6?-dimethylbiphenyl-3-yl]methoxy} -2,3-dihydro-1-benzofuran-3-yl)acetic acid), which acted as a GPR40/FFA1 agonist with in vivo efficacy during an oral glucose tolerance test (OGTT) in rats with impaired glucose tolerance.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3567O – PubChem

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805250-17-3, Name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate, belongs to benzofurans compound, is a common compound. Computed Properties of C11H12O4In an article, once mentioned the new application about 805250-17-3.

The present invention relates to a novel biphenyl heterocyclic derivative represented by a general formula (I) and a preparation method thereof and use of a pharmaceutical composition containing the derivative for preparation of a drug for treating diabetes. The biphenyl heterocyclic derivative has extremely excellent hypoglycemic activity in vivo, and excellent in vivo safety and low liver toxicity risk of the compound having such a structure are unexpectedly found, and the novel biphenyl heterocyclic derivative may be used for preventing or treating diabetes.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3540O – PubChem

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Chemistry is traditionally divided into organic and inorganic chemistry. Formula: C11H12O4, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 805250-17-3

The present invention relates to thioaryl derivatives of Formula 1 as defined in the specification, a method for preparing the same, a pharmaceutical composition comprising the same and use thereof. The thioaryl derivatives of Formula 1 according to the present invention promote GLP-1 formation in the gastrointestinal tract and improve insulin resistance in macrophages, pancreas cells, etc. due to anti-inflammatory action, and can accordingly be effectively used for preventing or treating diabetes, complications of diabetes, inflammation, obesity, non-alcoholic fatty liver, steatohepatitis or osteoporosis.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3544O – PubChem

Brief introduction of 805250-17-3

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Synthetic Route of 805250-17-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.805250-17-3, Name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate, molecular formula is C11H12O4. In a article,once mentioned of 805250-17-3

The present invention relates to compounds of general formula I, wherein the groups (Het)Ar and R1 are defined as in claim 1, which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3535O – PubChem

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Application of 805250-17-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.805250-17-3, Name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate, molecular formula is C11H12O4. In a article,once mentioned of 805250-17-3

The free fatty acid receptor 1 (FFA1/GPR40) is a novel antidiabetic target based on particular mechanism in enhancing glucose-stimulated insulin secretion. Most of reported FFA1 agonists, however, have been suffered from relatively high lipophilicity and molecular weight. Aiming to develop potent agonists with improved physicochemical property, 25 compounds containing triazole scaffold and various carboxylic acid fragments were synthesized via the click chemistry. Among them, the optimal lead compound 26 with relatively low lipophicity (Log D7.4 = 1.95) and molecular weight (Mw = 391.78) exhibited a considerable FFA1 agonistic activity (36.15%). In addition, compound 26 revealed a significant improvement in the glucose tolerance with a 21.4% and 14.2% reduction of glucose AUC0?2hin normal ICR mice and type 2 diabetic C57BL/6 mice, respectively. All of these results demonstrated that compound 26 was considered to be a promising lead compound suitable for further optimization.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3565O – PubChem

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Chemistry is traditionally divided into organic and inorganic chemistry. Product Details of 805250-17-3, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 805250-17-3

The present invention relates to biphenyl derivatives, its preparation method and its pharmaceutical composition and use in medicine. Specifically, the invention relates to a new urea-biphenyl derivatives, its pharmaceutical composition and its preparation method, further relates to the biphenyl derivative and or containing the pharmaceutical composition as a therapeutic agent, in particular as GPR40 agonists and in preparation for the treatment of diabetes and metabolic disorders and other diseases in use. The invention relates to compounds containing carry urethane, this group in the structure of this type of compound with the uniqueness and novelty. (by machine translation)

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3553O – PubChem

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Product Details of 805250-17-3, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 805250-17-3, name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate. In an article£¬Which mentioned a new discovery about 805250-17-3

A amide structure of the GPR40 agonist compound and use thereof (by machine translation)

The invention relates to a novel structure of the amide compound and its pharmaceutical composition, the compound of structure such as states the acid radical of the general formula (I) is shown. The amide compound (I) can regulate the GPR40 activity, can be used for GPR40 activity related diseases such as diabetes mellitus and metabolic syndrome. (by machine translation)

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Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H3549O – PubChem

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The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 805250-17-3 is helpful to your research. Related Products of 805250-17-3

Related Products of 805250-17-3, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 805250-17-3, molcular formula is C11H12O4, introducing its new discovery.

Design, synthesis and structure?activity relationship studies of GPR40 agonists containing amide linker

Free fatty acid receptor 1 (FFAR1/GPR40) attracted significant attention as a potential target for developing novel antidiabetic drugs because of its unique mechanism in glucose homeostasis. Several reports have expressed concerns about central nervous system (CNS) penetration of GPR40 agonists, which is possibly attributed to their high lipophilicity and low total polar surface area. Herein, we report our efforts to improve the physicochemical properties and pharmacokinetic profiles of LY2881835, a GPR40 agonist that had undergone Phase I clinical trial, through a series of structural optimizations. We identified an orally efficacious compound, 15k, which possessed increased plasma exposure, prolonged half-life and reduced CNS exposure and liver to plasma distribution ratio compared with LY2881835. 15k is a potentially valuable lead compound in the development of safe and efficacious GPR40-targeted drugs to treat type 2 diabetes mellitus.

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Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H3559O – PubChem

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Related Products of 805250-17-3, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 805250-17-3, Name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate,introducing its new discovery.

Discovery of novel pyrrole-based scaffold as potent and orally bioavailable free fatty acid receptor 1 agonists for the treatment of type 2 diabetes

The free fatty acid receptor 1 (FFA1) has gained significant interest as a novel antidiabetic target. Most of FFA1 agonists reported in the literature bearing a common biphenyl scaffold, which was crucial for toxicity verified by the researchers of Daiichi Sankyo. Herein, we describe the systematic exploration of non-biphenyl scaffold and further chemical modification of the optimal pyrrole scaffold. All of these efforts led to the identification of compound 11 as a potent and orally bioavailable FFA1 agonist without the risk of hypoglycemia. Further molecular modeling studies promoted the understanding of ligand-binding pocket and might help to design more promising FFA1 agonists.

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Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H3562O – PubChem

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 805250-17-3, name is Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate, introducing its new discovery. Safety of Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate

BIPHENYL COMPOUNDS AND USES THEREOF

The present invention relates to biphenyl compounds and uses thereof in medicine. Specifically, the present invention relates to a compound of Formula (I), or a stereoisomer, a geometric isomer, a tautomer, a mesomer, a racemate, an enantiomer, a diastereoisomer, an N-oxide, a hydrate, a solvate, a metabolite, a hydrolysate, a pharmaceutically acceptable salt or a prodrug thereof. The compound disclosed herein is used as a therapeutic agent particularly a GPR40 agonist for treating diabetes and metabolic disease in a patient.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 805250-17-3, and how the biochemistry of the body works.Safety of Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate

Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H3557O – PubChem