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| 编号: | 118049 |
| 中文名称: | FMOC-L-炔丙基甘氨酸 |
| 英文名: | Fmoc-Gly(Propargyl)-OH |
| CAS号: | 198561-07-8 |
| 单字母: | Fmoc-Pra-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。 -Pra炔丙基甘氨酸 -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: | C20H17O4N1 |
| 平均分子量: | 335.35 |
| 精确分子量: | 335.12 |
| 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 |
Fmoc-Pra-OH is a bioconjugate used in Click Chemistry. Click Chemistry is a chemical reaction that joins two components together by forming an amide bond between the carboxyl group of one component and the amino group on the other component. Fmoc-Pra-OH was synthesized by reacting the epidermal growth factor (EGF) with a cyclic peptide containing an acid moiety, which was conjugated to the azide group of an azidopropargyl linker. This bioconjugate has been shown to have proliferative activity in vitro and structural studies have been performed to understand its reactivity.





