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61.
乌头属植物的化学成分及药理作用研究进展 总被引：1，自引：0，他引：1
乌头属植物物种极为丰富，是我国重要的药用植物之一。对我国乌头属植物的化学成分和药理作用的研究近况进行了综述，以期为乌头属植物的开发利用提供一定参考。 相似文献
62.
Two new alkaloids were isolated from the bark of Sarcomelicope megistophylla. Cyclomegistine B (1), a new quinolone alkaloid, that possesses a rare cyclobuta[b]quinoline ring system and sarcomejine B (2) which is a quinolone alkaloid with an unusual side chain. The structure of both compounds was elucidated on the basis of MS data and extensive NMR studies. 相似文献
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披针叶黄华抗杉木炭疽菌活性物质研究 总被引：8，自引：0，他引：8
预试验中发现披针叶黄华地上部分乙醇浸提物具有抗杉木炭疽菌活性 ,进一步用不同溶剂 ,在不同 p H值下萃取得到 4个组分 .生测表明披针叶黄华中生物碱部分对杉木炭疽菌的抑菌活性最强 .其生物碱对杉木炭疽菌分生孢子萌发较对菌丝生长的抑制活性强 ,对杉木炭疽菌的分生孢子和菌丝的 EC50分别为 1 36.0 μg/m L和 1 555.0 μg/m L 相似文献
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Alkaloids are a large and structurally diverse group of marine-derived natural products. Most marine-derived alkaloids are biologically active and show promising applications in modern (agro)chemical, pharmaceutical, and fine chemical industries. Different approaches have been established to access these marine-derived alkaloids. Among these employed methods, biotechnological approaches, namely, (chemo)enzymatic synthesis, have significant potential for playing a central role in alkaloid production on an industrial scale. In this review, we discuss research progress on marine-derived alkaloid synthesis via enzymatic reactions and note the advantages and disadvantages of their applications for industrial production, as well as green chemistry for marine natural product research. 相似文献
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Murebwayire S Diallo B Luhmer M Vanhaelen-Fastré R Vanhaelen M Duez P 《Fitoterapia》2006,77(7-8):615-617
A new alkaloid, named gasabiimine (1), together with four known bisbenzyltetrahydroisoquinoline alkaloids (phaeanthine, 1,2-dehydroapateline, N-methylapateline, O-methylcocsoline) has been isolated from the roots of Triclisia sacleuxii. The structure of the new alkaloid was elucidated by spectroscopic data analysis. 相似文献
70.
Three new quinolone alkaloids, 1-methyl-2-[7-hydroxy-(E)-9-tridecenyl]-4(1H)-quinolone (1), 1-methyl-2-[(Z)-4-nonenyl]-4(1H)-quinolone (2), 1-methyl-2-[(1E,5Z)-1,5-undecadienyl]-4(1H)-quinolone (3) and one new natural product, 1-methyl-2-[(E)-1-undecenyl]-4(1H)-quinolone (4), were isolated from the dried and nearly ripe fruits of Evodia rutaecarpa (Juss.) Benth., along with thirteen known compounds (5-17). In addition, one new artificial product, 1-methyl-2-[7-carbonyl-(E)-9-tridecenyl]-4(1H)-quinolone (1A) was also obtained. The structures of these compounds were determined by spectroscopic analyses. The cytotoxic activities of all of the compounds against the human cancer cell lines HL-60, N-87, H-460, and Hep G(2) cells were evaluated by MTT assay. The results showed that these alkaloids inhibited cell proliferation with IC(50) values between 14μM and 22μM. 相似文献