- ￥696 - 18900
- TargetMol
- 美国
- T38063
- 2025年07月10日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
零下80~20°C
- 保质期：
Powder: -20°C for 3 years In solvent: -80°C for 2 years
- 英文名：
N-Acetyl lysyltyrosylcysteine amide
- 库存：
10
- 供应商：
TargetMol
- CAS号：
1287585-40-3
- 规格：
100 mg/50 mg/500 mg/1 mg/25 mg/5 mg/10 mg
| 规格： | 100 mg | 产品价格： | ￥9430.0 |
|---|---|---|---|
| 规格： | 50 mg | 产品价格： | ￥6860.0 |
| 规格： | 500 mg | 产品价格： | ￥18900.0 |
| 规格： | 1 mg | 产品价格： | ￥696.0 |
| 规格： | 25 mg | 产品价格： | ￥4890.0 |
| 规格： | 5 mg | 产品价格： | ￥1790.0 |
| 规格： | 10 mg | 产品价格： | ￥2970.0 |
Product Introduction
Bioactivity
英文名:N-Acetyl lysyltyrosylcysteine amide
描述:N-Acetyl lysyltyrosylcysteine amide is a non-toxic myeloperoxidase (MPO) tripeptide inhibitor that is potent, reversible, and specific.N-Acetyl lysyltyrosylcysteine amide effectively inhibits MPO production in vivo. N-Acetyl lysyltyrosylcysteine amide attenuates neuronal damage and preserves brain tissue and neurological function in the post-stroke brain.N-Acetyl lysyltyrosylcysteine amide inhibits MPO-dependent hypochlorite (HOCl) production, protein nitration and LDL oxidation.N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, and specific agent. N-Acetyl lysyltyrosylcysteine amide is used in the study of bronchial dysplasia.
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文献和实验Analysis of Fatty Acid Amide Hydrolase Activity in Plants
N -Acylethanolamines (NAEs) are fatty acid derivatives amide-linked to ethanolamine. NAEs vary in chain lengths and numbers of double bonds and generally reflect the fatty acids found in membrane lipids in the tissues in which they reside
The 1,5-Disubstituted Tetrazole Ring as a cis-Amide Bond Surrogate
Proline occupies a special role among those amino acids incorporated into peptides and proteins by the normal ribosomal pathways, since it is the only residue that leads to an N -alkyl amide bond. In peptide natural products
Backbone Amide Linker Strategies for the Solid-Phase Synthesis of C - Terminal Modified Peptides
This chapter describes backbone amide linker (BAL) strategies for the N α-Fmoc solid-phase synthesis of C-terminal modified peptides. Most solid-phase protocols for the assembly of such peptides have limited generality, because they rely on the C
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