More research is needed about 3-Aminopiperidine-2,6-dione hydrochloride

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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, 24666-56-6, molcular formula is C5H9ClN2O2, introducing its new discovery. name: 3-Aminopiperidine-2,6-dione hydrochloride

DETERMINING SMALL MOLECULE-PROTEIN AND PROTEIN-PROTEIN INTERACTIONS

Provided herein are methods, systems, kits, and compositions useful for determining small molecule-protein interactions and protein-protein interactions. The photo-click tags provided herein can be conjugated to a small molecule or amino acid analog to provide compounds that can be integrated into a protein through photo-conjugation, allowing for identification of a small molecule-protein interaction or protein-protein interaction to elucidate the small molecules mechanism of action or the protein targeted by the small molecule. In some embodiments, the photo-click tags comprise a photo-conjugation moiety and a click chemistry handle, allowing for the attachment of various functional groups (e.g., affinity tags) to the small molecule or amino acid analog.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, name: 3-Aminopiperidine-2,6-dione hydrochloride, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 24666-56-6

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H9508N – PubChem