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L selenocystine secys2

Manufactured by Thermo Fisher Scientific
Sourced in Japan, United States

L-selenocystine (SeCys2) is a laboratory reagent used in various research and analytical applications. It is a selenium-containing amino acid that can serve as a source of selenium in biochemical studies and experiments.

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2 protocols using l selenocystine secys2

1

Bioselenocompounds: Structural Diversity and Biological Significance

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Sodium selenate and potassium selenocyanate (SeCN) were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). Sodium selenite and seleno-l-methionine (SeMet) were purchased from Nacalai Tesque (Kyoto, Japan). Se-Methylseleno-l-cysteine (MeSeCys) and l-selenocystine (SeCys2) were purchased from Acros Organics (Waltham, MA) and Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan), respectively. Trimethylselenonium iodide (TMSe+) was purchased from Tri Chemical (Uenohara, Japan). l-Selenohomolanthionine (SeHLan) and 1β-methylseleno-N-acetylgalactosamine (SeSug1) were synthesized in our laboratory in accordance with our previous work [7 ,8 (link)]. The chemical structures of the bioselenocompounds used in this study are shown in Fig. 1.

Structures of bioselenocompounds used in this study. SeCN: selenocyanate, SeMet: selenomethionine, MeSeCys: Se-methylselenocysteine, SeHLan: selenohomolanthionine, SeCys2: selenocystine, SeSug1: 1β-methylseleno-N-acetylgalactosamine, TMSe+: trimethylselenonium ion.

Fig. 1
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2

Synthesis of Selenocompounds for Biological Study

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Sodium selenate and potassium selenocyanate (SeCN) were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). Sodium selenite and seleno-l-methionine (SeMet) were purchased from Nacalai Tesque (Kyoto, Japan). Se-Methylseleno-l-cysteine (MeSeCys) and l-selenocystine (SeCys2) were purchased from Acros Organics (Waltham, MA, USA) and Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan), respectively. Trimethylselenonium iodide (TMSe+) was purchased from Tri Chemical (Uenohara, Japan). l-Selenohomolanthionine (SeHLan) and Se-methylseleno-N-acetylgalactosamine (SeSug1) were synthesized in our laboratory in accordance with our previous work [6 (link),8 (link)]. The chemical structures of the bioselenocompounds used in this study are shown in Figure 1.
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