Dipartimento di Scienze Biochimiche "A. Rossi Fanelli" and Centro di Biologia Molecolare del CNR, Università di Roma "La Sapienza", Piazzale Aldo Moro, 5, I-00185, Roma, Italy.
Amino Acids. 1993 Feb;5(1):23-32. doi: 10.1007/BF00806189.
The products of autoxidation of S-aminoethyl-L-cysteine ketimine (AECK) have been analysed with the amino acid analyzer, with thin layer chromatography and with high performance liquid chromatography. Under the conditions of the assay (pH 8.5, 38°C, O2 bubbling) AECK is almost totally oxidized in 1.5 hours. Among the final products a component running fast in HPLC, named Cx1, has been isolated, reduced with NaBH4 and analysed. Reduced Cx1 resulted to show the same properties of synthetic thiomorpholine-3-carboxylic acid-S-oxide, known in the past literature with the name of "chondrine". On the basis of these results and by specific chromatographic tests, Cx1 has been identified as the sulfoxide of AECK. Among the other autoxidation products, thiomorpholine-3-one has been identified. The detection, after HCl hydrolysis, of glyoxylic acid and mesoxalic semialdehyde together with cysteamine indicates that compounds provided with easily cleavable S-C bonds, possibly thiohemiacetals or (and) thioesters, are the likely intermediates for other products. AECK sulfoxide and thiomorpholine-3-one are relatively stable and cannot be taken as the main intermediates for the remaining oxidation products.
用氨基酸分析仪、薄层层析和高效液相色谱法对 S-氨乙基-L-半胱氨酸酮亚胺(AECK)的自动氧化产物进行了分析。在测定条件下(pH8.5,38°C,通氧),AECK 在 1.5 小时内几乎完全氧化。在最终产物中,一种在 HPLC 中快速移动的成分 Cx1 被分离出来,用 NaBH4 还原并进行分析。还原后的 Cx1 表现出与过去文献中以“chondrine”命名的合成噻唑啉-3-羧酸-S-氧化物相同的性质。基于这些结果和特定的色谱测试,Cx1 被鉴定为 AECK 的亚砜。在其他自动氧化产物中,鉴定出了噻唑啉-3-酮。盐酸水解后检测到羟乙酸和甲亚磺酸半醛以及半胱氨酸胺表明,具有易断裂 S-C 键的化合物,可能是硫代半缩醛和/或硫代酯,是其他产物的可能中间体。AECK 亚砜和噻唑啉-3-酮相对稳定,不能作为剩余氧化产物的主要中间体。