克罗托福兰二甲:结构多样性,自然资源和治疗潜力
Hagar M Mohamed1,2, Gamal A Mohamed3, Sabrin R M Ibrahim4,5
1Department of Medical Laboratory Analysis, College of Medical and Health Sciences, Liwa University, Abu Dhabi, United Arab of Emirates.
Journal of pharmacy & bioallied sciences
|November 26, 2025
概括
这篇评论详细介绍了crotofolanes,这是来自Croton属的独特的diterpenoids. 它涵盖了它们的结构,起源,生物合成和重要的生物活动,如抗HIV和细胞毒性质.
科学领域:
- 自然产品化学 自然产品化学
- 植物化学 植物化学
- 药用化学 医学化学
背景情况:
- 克罗托福兰是一种独特的二烯类,其特点是合的三环形5/6/7环骨架.
- 这些化合物主要是从属于Croton属 (Euphorbiaceae) 的植物中分离出来的.
研究的目的:
- 综合审查和总结报告中的crotofolanes.
- 详细说明它们的来源,结构分类,生物合成和生物活动.
主要方法:
- 从1975年到2025年4月的crotofolane研究的文献综述.
- 对11个Croton物种的隔离数据的分析.
- 编制结构和生物活动信息.
主要成果:
- 共有62种crotofolane衍生物已被确定.
- 这些化合物表现出多样化的生物特性,包括抗HIV,抗疟疾,细胞毒性和免疫抑制活性.
- 结构变化源于明显的氧化变化和重新排列.
结论:
- 克罗托福兰体代表着结构多样化和生物学上重要的四平类动物.
- 对crotofolanes的进一步研究可能会产生新的治疗剂.
更多相关视频
相关概念视频
Drugs that Stabilize Microtubules
2.6K
Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
2.6K
Drugs that Destabilize Microtubules
3.6K
Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
3.6K
Structure-Activity Relationships and Drug Design
1.7K
Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
1.7K
Introduction to Plant Diversity
48.4K
From Water to Land
48.4K
Lipid-derived Compounds in the Human Body
6.2K
Fats and lipids are crucial components in the human body. Some lipid-derived compounds, such as fat-soluble vitamins, eicosanoids, lipoproteins, and glycolipids, also play unique roles to support various biological processes .
Fat-soluble Vitamins
Fat-soluble vitamins, including vitamins A, D, E, and K, are required in minimal quantities, but their deficiencies can lead to severely abnormal physiological conditions. For example, vitamin A deficiency can cause night blindness, dry skin,...
Fat-soluble Vitamins
Fat-soluble vitamins, including vitamins A, D, E, and K, are required in minimal quantities, but their deficiencies can lead to severely abnormal physiological conditions. For example, vitamin A deficiency can cause night blindness, dry skin,...
6.2K
Targets for Drug Action: Overview
10.0K
Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
10.0K


