Matrine family derivatives: Synthesis, reactions procedures, mechanism, and application in medicinal, agricultural, and materials chemistry

Matrine alkaloid is a type of Sophora flavescens (Ku Shen) found in plants. It holds excellent applications for anticancer, antimicrobials, antibacterial, anti pests, and other applications in material chemistry such as electrochemical. Owing to its superior biological and pharmaceutical properties...

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Main Authors: Jamal A.H. Kowah (Author), Ruobing Gao (Author), Fu Li (Author), Chenxi Guang (Author), Meiyan Jiang (Author), Xiaolin Wu (Author), Lisheng Wang (Author), Xu Liu (Author)
Format: Book
Published: Elsevier, 2023-04-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jamal A.H. Kowah  |e author 
700 1 0 |a Ruobing Gao  |e author 
700 1 0 |a Fu Li  |e author 
700 1 0 |a Chenxi Guang  |e author 
700 1 0 |a Meiyan Jiang  |e author 
700 1 0 |a Xiaolin Wu  |e author 
700 1 0 |a Lisheng Wang  |e author 
700 1 0 |a Xu Liu  |e author 
245 0 0 |a Matrine family derivatives: Synthesis, reactions procedures, mechanism, and application in medicinal, agricultural, and materials chemistry 
260 |b Elsevier,   |c 2023-04-01T00:00:00Z. 
500 |a 2772-4174 
500 |a 10.1016/j.ejmcr.2022.100098 
520 |a Matrine alkaloid is a type of Sophora flavescens (Ku Shen) found in plants. It holds excellent applications for anticancer, antimicrobials, antibacterial, anti pests, and other applications in material chemistry such as electrochemical. Owing to its superior biological and pharmaceutical properties over the past decade, pharmaceutical researchers have demonstrated that matrine can defeat the proliferation of various cancer cells, such as the proliferation of the human erythroleukemia cell line K562 and human hepatic cancer cell line SMMC-7721. This review mainly highlights the recent progress of matrine in synthesis, reaction procedures, mechanisms, and applications in medicinal, agricultural, and materials chemistry. In addition, we have also paid attention to the reactivity of matrine rings with different positions, including reactivity in N-1, C-13, C-14, (A, B, C) rings, carbonyl group at 15 positions, and amide bond at 15 and 16 positions, fused D-ring, opened A, B, and D-ring, via structural simplification, and total synthesis and design of matrine analogues from other compounds with different strategies. Particularly, the reported strategies were conducted in classical and non-classical conditions, mainly green conditions such as green solvents, catalysts, and other procedures. 
546 |a EN 
690 |a Matrine derivatives 
690 |a Synthesis 
690 |a Design and mechanism 
690 |a Application 
690 |a Structural modifications 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
690 |a Other systems of medicine 
690 |a RZ201-999 
655 7 |a article  |2 local 
786 0 |n European Journal of Medicinal Chemistry Reports, Vol 7, Iss , Pp 100098- (2023) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S277241742200070X 
787 0 |n https://doaj.org/toc/2772-4174 
856 4 1 |u https://doaj.org/article/1d7d6624c40b4eb9ad1567ffe203029d  |z Connect to this object online.