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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
2-8°C储存;充氩
- 英文名:
N-Fmoc-L-glutamic acid 1-tert-butyl ester
- 库存:
现货
- 供应商:
上海阿拉丁生化科技股份有限公司
- 规格:
N136487-5g/N136487-500g/N136487-25g/N136487-250mg/N136487-1g/N136487-100g
| 规格: | N136487-5g | 产品价格: | ¥88.9 |
|---|---|---|---|
| 规格: | N136487-500g | 产品价格: | ¥4500.9 |
| 规格: | N136487-25g | 产品价格: | ¥419.9 |
| 规格: | N136487-250mg | 产品价格: | ¥25.9 |
| 规格: | N136487-1g | 产品价格: | ¥26.9 |
| 规格: | N136487-100g | 产品价格: | ¥1499.9 |
英文名:N-Fmoc-L-glutamic acid 1-tert-butyl ester
纯度或规格:≥98%
SPU:N136487
CAS:84793-07-7
存储温度:2-8°C储存;充氩
运输条件:低温运输
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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
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