15/9/2021 News Properties and Exciting Facts About 31140-42-8

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Synthetic Route of 31140-42-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.31140-42-8, Name is 3-Boc-Amino-2,6-dioxopiperidine, molecular formula is C10H16N2O4. In a Article,once mentioned of 31140-42-8

The use of small molecules to regulate cellular levels of specific proteins is poised to become a powerful technique in the coming years. Critical to the success of any project utilizing such an approach will be the ability to synthesize libraries of candidate small molecules for testing in cellular systems. Herein, we describe a practical synthesis of a phthalimide-based scaffold, which can be easily diversified to make Cereblon-targeting PROTACs. We demonstrate the effectiveness of this approach by synthesizing a ?PROTAC toolbox? of four amines which can be coupled to inhibitors in a straightforward manner.

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Reference:
Piperidine – Wikipedia,
Piperidine | C5H18317N – PubChem

 

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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, 31140-42-8, molcular formula is C10H16N2O4, introducing its new discovery. Quality Control of: 3-Boc-Amino-2,6-dioxopiperidine

(Matrix presented) A five-step synthesis of an azido-thalidomide analogue is presented. The sequence requires cheap and readily available starting materials and reagents, and only two steps require purification. Additionally, the azido-labeled analogue possesses activity comparable to that of thalidomide in inhibiting the proliferation of human microvascular endothelial cells, thus providing impetus for its use as a potential photoaffinity label of thalidomide.

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Reference:
Piperidine – Wikipedia,
Piperidine | C5H18340N – PubChem

 

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Preliminary biological evaluations of new thalidomide analogues for multiple sclerosis application

The present work deals with the synthesis of a new series of thalidomide derivatives for therapeutic applications. These compounds were evaluated in vitro on a human endothelial cell line EA.hy926 for their antiproliferative potential and in vivo on an experimental animal multiple sclerosis model called EAE as angiogenesis inhibitors. The preliminary results obtained on EAE assays seem to validate that anti-angiogenesis compounds could be promising tools for the treatment of MS.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H18319N – PubChem

 

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The synthetic route of 31140-42-8 has been constantly updated, and we look forward to future research findings.

31140-42-8, 3-Boc-Amino-2,6-dioxopiperidine is a piperidines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

To a solution of tert-butyl (2-78, 2,6-dioxopiperidin-3-yl)carbamate (1.0 g, 4.38 mmol) in THF (15 mL) was added NaH (263 mg, 6.57 mmol) at 0 C. After stirring for 20 minutes at room temperature, iodomethane (327 muL, 5.26 mmol) was added to the reaction mixture. After stirring for 2 hours, the mixture was diluted with EtOAc and quenched with water. The organic layer was collected and the aqueous layer was washed with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated. The crude compound 2-79 was carried forward in the next step without additional purification., 31140-42-8

The synthetic route of 31140-42-8 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; DANA FARBER CANCER INSTITUTE, INC.; GRAY, Nathanael; JANG, Jaebong; DE CLERCQ, Dries; ECK, Michael; (201 pag.)WO2017/185036; (2017); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem