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In order to discover a novel type of analgesic, we investigated dual activity ligands with TRPV1 antagonism and mu-opioid receptor affinity with the goal of eliciting synergistic analgesia while avoiding the side effects associated with single targeting. Based on a combination approach, a series of 4-benzyl-4-(dimethylamino)piperidinyl analogues were designed, synthesized and evaluated for their receptor activities. Among them, compound 49 exhibited the most promising dual-acting activity toward TRPV1 and the mu-opioid receptor in vitro. In vivo, 49 displayed potent, dose-dependent antinociceptive activity in both the 1st and 2nd phases in the formalin assay. Consistent with its postulated mechanism, we confirmed that in vivo, as in vitro, compound 49 both antagonized TRPV1 and functioned as a mu-opioid agonist. This result indicates that dual-acting TRPV1 antagonist/mu-opioid ligands can be made and represent a new and promising class of analgesic.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2445O – PubChem

The important role of 6,7-Dimethoxy-3H-1-isobenzofuranone

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The compounds of formula (I) of the subject invention are related to 2-substituted cephem compounds, which have a wide antimicrobial spectrum, in particular exhibit potent antimicrobial activity against beta-lactamase producing Gram negative bacteria, and pharmaceutical compositions comprising the same.

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Benzofuran – Wikipedia,
Benzofuran | C8H3124O – PubChem

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Related Products of 10242-10-1, 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.10242-10-1, Name is 5-Chlorobenzofuran-2-carboxylic acid, molecular formula is C9H5ClO3. In a article,once mentioned of 10242-10-1

Compounds of formula (I) wherein X is a fluorine or a chlorine atom; the methyl groups located at the 2- and 5-position of the piperazine ring are in trans-configuration to each other; Y is NH or O; R1 is selected front hydrogen, chloro, bromo, nitro, methyl or trifluoromethyl; R2 is selected from hydrogen, halo, methyl, trifluoromethyl, methoxy or trifluoromethoxy; or a pharmaceutically acceptable salt or solvate thereof, The invention also relates to pharmaceutical compositions containing a compound of formula (I) together with a pharmaceutically acceptable carrier. Included are also processes for the preparation of compounds of formula (I), as well as methods for treating mammals suffering from inflammatory, autoimmune, proliferative or hyperproliferative diseases by administering a compound having the formula (I) to said mammal.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3168O – PubChem

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This invention provides novel 5-HT 1F agonists of the Formula STR1 in which X, Y, E, R, A, B, and n are as defined in the specification, which are useful for the treatment of migraine and associated disorders.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H365O – PubChem

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Application of 54109-03-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.54109-03-4, Name is 5-Chloroisobenzofuran-1(3H)-one, molecular formula is C8H5ClO2. In a Article,once mentioned of 54109-03-4

Versatile, simple and inexpensive ligand-free, copper-catalyzed N-arylations of sulfoximines and nitrogen-containing heterocycles have been developed affording N-arylated products in high yields.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2613O – PubChem

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of 3-Hydroxyisobenzofuran-1(3H)-one, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 16859-59-9, Name is 3-Hydroxyisobenzofuran-1(3H)-one, molecular formula is C8H6O3

A series of isobenzofuran-1(3H)-ones (phthalides), analogues of the naturally occurring phytotoxin cryphonectric acid, were designed, synthesized, and fully characterized by NMR, IR, and MS analyses. Their synthesis was achieved via condensation, aromatization, and acetylation reactions. The measurement of the electron transport chain in spinach chloroplasts showed that several derivatives are capable of interfering with the photosynthetic apparatus. Few of them were found to inhibit the basal rate, but a significant inhibition was brought about only at concentrations exceeding 50 muM. Some other analogues acted as uncouplers or energy transfer inhibitors, with a remarkably higher effectiveness. Isobenzofuranone addition to the culture medium inhibited the growth of the cyanobacterium Synechococcus elongatus, with patterns consistent with the effects measured in vitro upon isolated chloroplasts. The most active derivatives, being able to completely suppress algal growth at 20 muM, may represent structures to be exploited for the design of new active ingredients for weed control.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H1503O – PubChem

A new application about Benzofuran-4-carboxylic acid

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Electric Literature of 166599-84-4, 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, 166599-84-4, molcular formula is C9H6O3, introducing its new discovery.

The invention relates to a azacitidine preparation method, the method avoids azacitidine contact water, reduce azacitidine degradation, not only simple operation, greatly improving the yield and purity. In addition, in the azacitidine further in the purification process, the invention the use of ethanol as a solvent of the crystal, the cost is greatly reduced, more suitable for industrial application. (by machine translation)

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H1615O – PubChem

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We report the total synthesis of an alkaloid isolated from the mangrove fungi Hypocrea virens, based on the originally claimed structure, via a photochemical sequence. Inconsistencies between data sets led to a revision of the proposed structure followed by a concise synthetic sequence to deliver the revised natural product.

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Benzofuran – Wikipedia,
Benzofuran | C8H1458O – PubChem

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A series of novel amide-based small molecule inhibitors of inosine monophosphate dehydrogenase (IMPDH) was explored. The synthesis and the structure-activity relationships (SARs) derived from in vitro studies are described.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2017O – PubChem

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Reference of 13196-11-7, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 13196-11-7, Name is Benzofuran-6-ol, molecular formula is C8H6O2. In a Patent,once mentioned of 13196-11-7

Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette (“”ABC””) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator (“”CFTR””). The present invention also relates to methods of treating CFTR mediated diseases using compounds of the present invention.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H398O – PubChem