Yuzurimine-type alkaloids
Yuzurimine-type alkaloids are a class of nitrogen-containing natural products isolated from plants, particularly those belonging to the genus *Zanthoxylum*. These alkaloids exhibit diverse biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties. The yuzurimine structure typically consists of a core indole ring system with an attached pyrrole or pyridine moiety, creating unique chemical functional groups that contribute to their pharmacological potential. Due to their structural complexity, these alkaloids are often targets for pharmaceutical research aimed at developing new therapeutic agents. Their isolation and purification from natural sources involve intricate extraction methods followed by sophisticated chromatographic techniques. Yuzurimine-type alkaloids have garnered significant interest in the scientific community due to their promising medicinal applications.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Methyl (1R,2S,5S,8R)-2,6-dimethyl-8-oxido-20-oxo-8-azoniahexacyclo[11.5.1.11,5.02,10.03,8.016,19]icosa-13(19),16-diene-17-carboxylate | 1092555-02-6 | C23H29NO4 |
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Longistylumphylline A | 857672-34-5 | C23H29NO3 |
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Daphniyunnine A | 881388-87-0 | C23H31NO3 |
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Daphnilongeranine C; 21-Acetoxy, Me ester, N-oxide | 753450-66-7 | C25H33NO6 |
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Daphnilongeranine C; 21-Acetoxy, Me ester, N-oxide, conformational isomer | 753450-64-5 | C25H33NO6 |
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Daphnilongeranine C; 6'-Ester with #JFB06-M | 752252-75-8 | C38H49NO12 |
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Daphnilongeranine C; 4S-Hydroxy, 14,15-didehydro, Me ester | 1818395-42-4 | C23H29NO4 |
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subdaphnidine A | 1186496-67-2 | C25H33NO5 |
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Daphnilongeranin C | 750649-07-1 | C22H29NO3 |
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Daphniglaucine B | 543701-04-8 | C24H34NO4 |
Related Literature
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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