Napelline-type diterpenoid alkaloids
Napelline-type diterpenoid alkaloids are a class of natural products isolated from various species of plants, particularly those in the genus *Aconitum* (monkshood). These compounds exhibit a variety of pharmacological activities including analgesic, anti-inflammatory, and cytotoxic effects. Structurally, napelline-type diterpenoid alkaloids typically feature a diterpene core with characteristic substitution patterns that include various functional groups such as hydroxyls, methoxyls, and amino acids. Notably, these alkaloids often contain unique nitrogen-containing rings that contribute to their complex structure and bioactivity profiles. Research on napelline-type diterpenoid alkaloids has revealed potential applications in drug development for the treatment of pain syndromes, inflammation, and certain types of cancer due to their selective binding properties and modulatory effects on cellular pathways.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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napelline | 5008-52-6 | C22H33NO3 |
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Songorine | 509-24-0 | C22H31NO3 |
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12-acetylluciculine | 62511-84-6 | C24H35NO4 |
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1-acetylluciculine | 68676-52-8 | C24H35NO4 |
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luciculine | 110064-70-5 | C22H33NO3 |
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(20S)-1α,15β-Dihydroxy-4β-methyl-16-methylene-7α,20-cycloveatchan-12-one | 29722-71-2 | C20H27NO3 |
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Napelline; 12-Epimer, 12-Ac | 2171318-89-9 | C24H35NO4 |
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Napelline; 11β-Hydroxy | 169626-33-9 | C22H33NO4 |
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12-epi-15-O-acetylnapelline | 5008-49-1 | C24H35NO4 |
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liangshanine | 137031-43-7 | C23H35NO3 |
Related Literature
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Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
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Yuan-Jun Tong,Lu-Dan Yu,Lu-Lu Wu,Shu-Ping Cao,Ru-Ping Liang,Li Zhang,Xing-Hua Xia,Jian-Ding Qiu Chem. Commun., 2018,54, 7487-7490
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Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
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M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
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