Ethyl (S)-(+)-2-pyrrolidinone-5-carboxylate
CAS: 7149-65-7
Ref. 3D-FE05980
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Información del producto
- (2S)-5-Oxopyrrolidine-2-carboxylic acid ethyl ester
- (S)-(+)-Ethyl 2-pyrrolidone-5-carboxylate
- (S)-Ethyl 5-oxopyrrolidine-2-carboxylate
- <span class="text-smallcaps">L</span>-2-Ethoxycarbonyl-5-pyrrolidone
- <span class="text-smallcaps">L</span>-Proline, 5-oxo-, ethyl ester
- <span class="text-smallcaps">L</span>-Pyroglutamic acid ethyl ester
- Ethyl (2S)-5-oxopyrrolidine-2-carboxylate
- Ethyl (S)-pyroglutamate
- Ethyl 5-oxo-<span class="text-smallcaps">L</span>-prolinate
- Ethyl <span class="text-smallcaps">L</span>-2-oxo-5-pyrrolidinecarboxylate
- Ver más sinónimos
- Ethyl <span class="text-smallcaps">L</span>-2-pyrrolidone-5-carboxylate
- Ethyl <span class="text-smallcaps">L</span>-pyroglutamate
- Ethyl L-pyroglutamate
- Ethyl pyroglutamate
- L-Pyroglutamic Acid Ethyl Ester
- NSC 166529
- NSC 72279
- Proline, 5-oxo-, ethyl ester, <span class="text-smallcaps">L</span>-
- Pyr-Oet
- Pyroglutamic acid ethyl ester
Ethyl (S)-(+)-2-pyrrolidinone-5-carboxylate is a potent inhibitor of plasma glucose levels. It inhibits chemical reactions by acting as a nucleophile, attacking the carbonyl group at the anomeric carbon. This reaction causes the ring to open and form an amide. Ethyl (S)-(+)-2-pyrrolidinone-5-carboxylate has been shown to have stereoselective effects in vitro, inhibiting 3-o-caffeoylquinic acid production in human erythrocytes. It also inhibits amide bond formation and fatty esters synthesis in vitro, leading to decreased lipid level. Ethyl (S)-(+)-2-pyrrolidinone-5-carboxylate also has anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis.
Propiedades químicas
Consulta técnica sobre: 3D-FE05980 Ethyl (S)-(+)-2-pyrrolidinone-5-carboxylate
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