- ￥1900
- 伊塔生物
- 中国/进口
- YT07936
- 2025年10月29日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
1
- 保质期：
3年
- 英文名：
Fmoc-Lys(Fmoc)-王树脂
- 库存：
68
- 供应商：
北京伊塔生物科技有限公司
- CAS号：
13321
- 规格：
25g
| YT03514 | 叔丁氧羰基-甲苯磺酰基-精氨酸 | Boc-Arg(Tos)-OH | 13836-37-8 | 5g | 瓶 |
| YT03516 | N-芴甲氧羰基-N'-甲苯磺酰基-L-精氨酸 | Fmoc-Arg(Tos)-OH | 83792-47-6 | 1g | 瓶 |
| YT03518 | 磷脂聚乙二醇氨基 | DSPE-PEG-NH2 | \N | 1g | 瓶 |
| YT03520 | 生物素聚乙二醇氨基 | Biotin-PEG-NH2 | \N | 1g | 瓶 |
| YT03522 | 葫芦巴胶 | 1kg | 瓶 |
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文献和实验Solid-Phase Synthesis of Neuropeptides by Fmoc Strategies
an automated peptide synthesizer that performs solid-phase peptide synthesis using the Fmoc strategy (1 ). This is based on the sequential addition of amino acid residues to an insoluble polymeric support. The base-labile Fmoc group
. Therefore, guanidinium functional group is considered as an important pharmacophoric element. Although a number of methods for solid-phase guanidinylation reactions exist, only a few are fully compatible with standard Fmoc solid-phase peptide
Synthesis of C-Terminal Peptide Thioesters Using Fmoc-Based Solid-Phase Peptide Chemistry
This chapter provides two protocols for the solid-phase synthesis of peptide thioesters using N α -Fmoc-protected amino acids. The first protocol is based on a so-called safety-catch linker, while the second relies on a backbone amide
