New explortion of 4-Fluoroisobenzofuran-1,3-dione

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Reference of 652-39-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.652-39-1, Name is 4-Fluoroisobenzofuran-1,3-dione, molecular formula is C8H3FO3. In a Patent,once mentioned of 652-39-1

Disclosed are piperidine-2,6-dione derivatives and treatment of ulcerative colitis.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2506O – PubChem

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Electric Literature of 652-39-1, 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, 652-39-1, molcular formula is C8H3FO3, introducing its new discovery.

The invention discloses a 3 – phthalic acid synthetic method, the raw material 3 – nitrophthalic acid is dissolved by acetyl chloride solvent dehydration is carried out, after the dehydration by the fluorination potassium […], then adding thionyl chloride to remove the by-product generated in the process of fluoro, purification to obtain the target compound 3 – phthalic acid. The invention relates to 3 – nitrophthalic acid as the synthetic 3 – phthalic acid raw material, the raw material is cheap, simple process, high yield; by adjusting the PH of the method, the product from the sulfolane solvent in very good separation out, solves the high boiling point of the solvent is not easily evaporated difficult; using acetyl chloride as dehydration solvent, not only replacing the drug control acetic anhydride, but also reduces the acetic anhydride in the dehydration process of the acetic acid by-product, mild reaction conditions after processing is simple and convenient. (by machine translation)

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2504O – PubChem

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Microwave promoted high yielding synthesis of 4-aminoquinoline-phthalimides was developed with an aim to evaluate their anti-plasmodial potential. The scaffolds with longer spacer length (n = 6, 8) between two pharmacophores and a halogen substituent on the phthalimide ring displayed good antiplasmodial activity. Compound 5w, with an optimum combination of hexyl chain as spacer along with a tetra-bromophthalimide ring proved to be most potent and non-cytotoxic among the series exhibiting an IC50 value of 0.10 muM.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2552O – PubChem

New explortion of 4-Fluoroisobenzofuran-1,3-dione

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The BET proteins BRD2, BRD3, and BRD4 play important roles in transcriptional regulation and can be degraded by proteolysis-targeting chimeras (PROTACs) for BET proteins. However, the lack of intra-BET proteins selectivity limits the scope of current degraders as probes for target validation and could lead to unwanted side effects or toxicity in a therapeutic setting. We describe herein the design, synthesis, and evaluation of PROTAC BET degraders, based on the BET inhibitor with selectivity for the first Bromodomain benzo[cd]indole-2-one, alkylamide linker and cereblon ligand thalidomide. Compound 15 potently and rapidly induces reversible, long-lasting, and unexpectedly selective removal of BRD4 and BRD2 over BRD3, which not only effectively inhibits cell growth in human acute leukemia cell lines, but also very effective in inhibiting solid tumors with low cytotoxic effect in the cell profiles of NCI 60 cell lines. Remarkable dependency on linker length was observed for BRD4-degrading and c-Myc-driven antiproliferative activities in acute myeloid leukemia cell line MV4-11. The small-molecular 15 represents a novel, potent, and selective class of BRD4 and BRD2 degraders for the development of therapeutics to treat cancers.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2513O – PubChem

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Related Products of 652-39-1, 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, 652-39-1, molcular formula is C8H3FO3, introducing its new discovery.

A convenient method has been developed for the synthesis of new trifluoromethyl-substituted 11H-isoindolo[2,1-a]benzimidazol-11-one derivatives from 3-nitro-5-trifluoromethyl-o-phenylenediamine and aromatic anhydrides on the surface of silica gel impregnated with ZnCl2 under solvent free microwave irradiation conditions.{A figure is presented}.

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Benzofuran – Wikipedia,
Benzofuran | C8H2548O – PubChem

Extended knowledge of 652-39-1

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Chemistry is traditionally divided into organic and inorganic chemistry. Computed Properties of C8H3FO3, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 652-39-1

A series of secondary amine-substituted isoindoline-1,3-dione-4-aminoquinolines were prepared via microwave heating and assayed for their anti-mycobacterial activities. The compound with a butyl chain as a spacer between the two pharmacophores and piperidine as the secondary amine component on the isoindoline ring was the most potent and non-cytotoxic among the synthesized compounds, exhibiting a minimum inhibitory concentration (MIC99) of 6.25 mug mL-1 against Mycobacterium tuberculosis.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2553O – PubChem

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Electric Literature of 652-39-1, 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.652-39-1, Name is 4-Fluoroisobenzofuran-1,3-dione, molecular formula is C8H3FO3. In a article,once mentioned of 652-39-1

The invention discloses a cyano-containing phthalic amide derivative and its preparation and application. The compounds of the invention is shown in formula I, In formula I, R1 Is methyl, halogen, nitro; R2 Is H or methyl; R3 Is H or methyl; m is 0, 1 or 2; n is 1 – 6 any integer; a is 1 – 3 any integer; Y is selected from halogen, nitro, C1 – C6 Alkyl, C1 – C6 Alkoxy, trifluoromethyl, seven […] and […] isopropyl in the at least one. Said compound and/or its in agriculture trial on the salt, and/or a stereoisomer thereof in the preparation of the agricultural chemical pesticide application. The compounds of this invention have excellent pesticidal activity, 0.25 mg/L under the dosage of lepidopteran pest Diamondback moth demonstrate very good active; its aquatic ecosystem in the bottom end of the food chain […] has low toxicity, low toxicity to aquatic organisms; the compounds of this invention have a reasonable eco-toxicity and environmental compatibility, which belongs to the high efficiency, low toxicity, green agricultural chemicals. (by machine translation)

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2488O – PubChem

Discovery of 4-Fluoroisobenzofuran-1,3-dione

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Reference of 652-39-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.652-39-1, Name is 4-Fluoroisobenzofuran-1,3-dione, molecular formula is C8H3FO3. In a Article,once mentioned of 652-39-1

The cytochrome bc1 complex (the bc1 complex or complex III) is an attractive target for the discovery of numerous pharmaceuticals and pesticides. In order to identify new lead structures for this target, a new series of molecules, N-(4-aryloxyphenyl)phthalimides, were designed and synthesized in a straightforward manner. Our design strategy was to introduce a 4-aryloxyphenyl group, a fragment which exhibited promising bc1 complex-inhibiting properties, into the aryl group of the valuable N-arylphthalimide backbone. Afterward, the biochemical evaluation of the newly synthesized compounds was carried out, and the results implied that several compounds demonstrated good activities against succinate-cytochrome reductase (SCR, a mixture of mitochondrial complex II and the bc1 complex). Further studies confirmed that 3e? a representative compound in this paper, was identified as an inhibitor of the bc1 complex. Furthermore, computational simulations were also performed to better understand binding of 3e? to the enzyme complex, which indicated that 3e? should bind to the Qo site of the bc1 complex. Consequently, we harbor the idea that this paper can provide a solid platform for synthesis and discovery of other bc1 complex inhibitors.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2517O – PubChem

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Development of highly effective, safe, and fast-acting anti-depressants is urgently required for the treatment of major depressive disorder. It has been suggested that targeting 5-HT2A and 5-HT2C in addition to inhibition of serotonin reuptake may be beneficial in generating anti-depressant agents with better pharmacology and less adverse effects. We have developed phthalazinone-based compounds that potently bind to 5-HT2A, 5-HT2C, and the serotonin transporter. The representative compounds 11j and 11l displayed strong binding affinities against these targets, and showed favorable toxicity profiles as determined by hERG binding and CYP inhibition assays. Furthermore, these compounds presented promising anti-depressant effects comparable to fluoxetine and also synergistic effects with fluoxetine in forced swimming test, which implicates these compounds can be developed to help the treatment of major depressive disorder.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2515O – PubChem

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Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. category: benzofuran, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 652-39-1, in my other articles.

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Compounds having the general structure A – L – B are presented wherein A and B are independently an E3 ubiquitin ligase protein binding ligand compound of formula 1A or 1 B. Pharmaceutical compositions comprising these compounds and methods of use are also presented.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2468O – PubChem