植物化学选Zanthoxylum armatum根,并探索其多醇含量和抗氧化活性
Saumya Agnihotri1, Preeti Dobhal1, Sayyed Ashfaqullah1
1Department of Botany, D.S.B. Campus, Kumaun University, Nainital, India.
Natural product research
|August 11, 2023
概括
这项研究分析了Zanthoxylum armatum根提取物,确定了37种化合物和显著的抗氧化活性. 亚酸是最丰富的多,表明潜在的健康益处.
科学领域:
- 植物化学 植物化学
- 药理学是指药理学,即药理学是指药理学.
- 自然产品化学 自然产品化学
背景情况:
- 桑托西 (Zanthoxylum armatum) 是一种具有传统药用用途的植物.
- 了解其根的化学特征对于验证其治疗潜力至关重要.
研究的目的:
- 为了研究Zanthoxylum armatum根甲醇提取物的化学成分.
- 评估其多醇含量和抗氧化剂潜力.
主要方法:
- 气色谱-质谱 (GC-MS) 用于化学分析.
- 高性能液体染色学 - 光二极管阵列 (HPLC-PDA) 用于的量化.
- 对抗氧化活性进行检测 (DPPH,金属化,FRAP).
主要成果:
- GC-MS确定了37种植物化学成分,包括 (+) - 素和保罗等显著化合物.
- 惠普LC分析显示,酸是最丰富的多,其次是酸和酸.
- 提取物表现出显著的抗氧化活性,具有高总,黄和含量.
结论:
- 桑托西 (Zanthoxylum armatum) 根提取物具有丰富的植物化学特征,具有相当大的抗氧化特性.
- 已识别的化合物和抗氧化剂潜力支持该植物的传统药用应用.
相关概念视频
Oxidative Cleavage of Alkenes: Ozonolysis
In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Reactions at the Benzylic Position: Oxidation and Reduction
The benzylic position describes the position of a carbon atom attached directly to a benzene ring. Benzene by itself does not undergo oxidation. In contrast, the benzylic carbon is quite reactive in the presence of strong oxidizing agents such as KMnO4 or H2CrO4. Therefore, alkylbenzenes are readily oxidized to benzoic acid, irrespective of the type of alkyl groups.
Oxidation of Phenols to Quinones
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Radical Autoxidation
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
Radical Oxidation of Allylic and Benzylic Alcohols
Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...


