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| 编号: | 120482 |
| 中文名称: | Fmoc-Lys(Boc)-OH |
| 中文同义词: | N-alpha-芴甲氧羰基-N-epsilon-叔丁氧羰基-L-赖氨酸 |
| 英文名: | Fmoc-Lys(Boc)-OH |
| 英文同义词: | N-alpha-FMOC-Nepsilon-BOC-L-Lysine |
| CAS号: | 71989-26-9 |
| 单字母: | Fmoc-K(Boc)-OH |
| 三字母: | Fmoc N端Fmoc保护,9-芴甲氧羰基(Fmoc)是伯胺和仲胺的保护基团。在固相肽合成(SPPS)中,它是氨基酸主链的常用保护基,因为它可以很容易地用哌啶去除,而不会干扰树脂和肽之间的酸不稳定连接体。 -Lys(Boc)侧链Boc保护的赖氨酸;叔丁氧羰基或叔丁氧羰基(Boc)是胺的保护基团。Boc基团可用强酸去除,如用三氟乙酸在二氯甲烷中去除,或用HCl在甲醇中去除。 -OHC端羧基:C-terminal carboxyl group。在肽或多肽链中含有游离羧基的氨基酸一端。在表示氨基酸序列时,通常将C端放在肽链的右边。 |
| 氨基酸个数: | 1 |
| 分子式: | C26H32O6N2 |
| 平均分子量: | 468.54 |
| 精确分子量: | 468.23 |
| 等电点(PI): | - |
| pH=7.0时的净电荷数: | - |
| 平均亲水性: | - |
| 疏水性值: | - |
| 消光系数: | - |
| 来源: | 人工化学合成,仅限科学研究使用,不得用于人体。 |
| 储存条件: | 负80℃至负20℃ |
| 标签: | Fmoc保护氨基酸 Boc保护氨基酸 赖氨酸类 |
Fmoc固相多肽合成中Fmoc保护的赖氨酸Lys
Fmoc-Lys(Boc)-OH is a monoclonal antibody that reacts with lysine residues. It is synthesized by reacting a solid phase support with an aliphatic hydrocarbon. The reactive functional group on the hydrocarbon terminates in an amine and forms an amide linkage to the amino terminus of the peptide. The hydroxyl terminus of the peptide is then reacted with a trifluoroacetic acid (TFA) ester of lysine in the presence of base. This reaction produces a TFA salt of Fmoc-Lys(Boc)-OH, which can be purified by high salt precipitation or reversed to produce Fmoc-Lys(Boc)-OH by treatment with base. Fmoc-Lys(Boc)-OH has been used as a reagent for chemical conjugation to fluorophores and other molecules such as biotin, avidin, strept





