• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

苦木科番荔枝属植物枝叶中的氧化阿朴啡和嘧啶-β-咔啉生物碱的抗锥虫活性。

Trypanocidal activity of oxoaporphine and pyrimidine-β-carboline alkaloids from the branches of Annona foetida Mart. (Annonaceae).

机构信息

LABORGANICS, Department of Chemistry, Federal University of Sergipe, 49100-000, São Cristóvão, SE, Brazil.

出版信息

Molecules. 2011 Nov 23;16(11):9714-20. doi: 10.3390/molecules16119714.

DOI:10.3390/molecules16119714
PMID:22113579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6264547/
Abstract

Phytochemical investigation of the branches of Annona foetida Mart. led to isolation from the CH(2)Cl(2) extract of four alkaloids: Atherospermidine (1), described for the first time in this species, liriodenine (2), O-methylmoschatoline (3), and annomontine (4). Their chemical structures were established on the basis of spectroscopic data from IR, MS, NMR (1D and 2D), and comparison with the literature. Compounds 2-4 showed potent trypanocidal effect when evaluated against epimastigote and trypomastigote forms of Trypanosoma cruzi.

摘要

从番荔枝科番荔枝属植物番荔枝的枝部分离得到 4 个生物碱:阿罗司帕定(1)、利罗定(2)、O-甲基毛果芸香碱(3)和番荔枝宁(4)。这是首次在该种植物中发现阿罗司帕定。根据红外光谱(IR)、质谱(MS)、核磁共振(1D 和 2D)等光谱数据并与文献进行比较,确定了它们的化学结构。化合物 2-4 对克氏锥虫的滋养体和鞭毛体形式具有很强的杀锥虫作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d3/6264547/ac18eff20646/molecules-16-09714-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d3/6264547/ac18eff20646/molecules-16-09714-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d3/6264547/ac18eff20646/molecules-16-09714-g001.jpg

相似文献

1
Trypanocidal activity of oxoaporphine and pyrimidine-β-carboline alkaloids from the branches of Annona foetida Mart. (Annonaceae).苦木科番荔枝属植物枝叶中的氧化阿朴啡和嘧啶-β-咔啉生物碱的抗锥虫活性。
Molecules. 2011 Nov 23;16(11):9714-20. doi: 10.3390/molecules16119714.
2
A pyrimidine-beta-carboline and other alkaloids from Annona foetida with antileishmanial activity.一种来自恶臭番荔枝的具有抗利什曼原虫活性的嘧啶-β-咔啉及其他生物碱。
J Nat Prod. 2006 Feb;69(2):292-4. doi: 10.1021/np050422s.
3
The antitumoral, trypanocidal and antileishmanial activities of extract and alkaloids isolated from Duguetia furfuracea.从皱叶黄肉楠中提取的生物碱的抗肿瘤、杀锥虫和抗利什曼原虫活性。
Phytomedicine. 2009 Nov;16(11):1059-63. doi: 10.1016/j.phymed.2009.03.019. Epub 2009 May 7.
4
Aporphine Alkaloids from Ocotea puberula with Anti-Trypanosoma Cruzi Potential - Activity of Dicentrine-β-N-Oxide in the Plasma Membrane Electric Potentials.来自柔毛肉豆蔻具有抗克氏锥虫潜力的阿朴菲生物碱——双苄基异喹啉-β-N-氧化物对质膜电位的活性
Chem Biodivers. 2021 Apr;18(4):e2001022. doi: 10.1002/cbdv.202001022. Epub 2021 Mar 1.
5
Annomontine, an alkaloid isolated from Annona purpurea, has anxiolytic-like effects in the elevated plus-maze.从紫玉盘(Annona purpurea)中分离出的生物碱安诺明具有高架十字迷宫样的抗焦虑作用。
Planta Med. 2011 Mar;77(4):322-7. doi: 10.1055/s-0030-1250406. Epub 2010 Oct 1.
6
Full NMR analysis of annomontine, methoxy- annomontine and N-hydroxyannomontine pyrimidine-beta-carboline alkaloids.
Magn Reson Chem. 2008 Jan;46(1):69-74. doi: 10.1002/mrc.2134.
7
In vitro activity of Rutaceae species against the trypomastigote form of Trypanosoma cruzi.芸香科植物对克氏锥虫无鞭毛体形式的体外活性。
J Ethnopharmacol. 2000 Nov;73(1-2):335-40. doi: 10.1016/s0378-8741(00)00315-9.
8
7,7-Dimethylaporphine alkaloids from the stem of Guatteriopsis friesiana.来自弗氏瓜馥木茎中的7,7-二甲基阿朴啡生物碱。
J Nat Prod. 2009 Aug;72(8):1516-9. doi: 10.1021/np800788n.
9
Cytotoxic aporphine alkaloids from leaves and twigs of Pseuduvaria trimera (Craib).来自三瓣暗罗(Pseuduvaria trimera (Craib))叶和嫩枝的细胞毒性阿朴啡生物碱。
Molecules. 2014 Jun 25;19(7):8762-72. doi: 10.3390/molecules19078762.
10
Two new β-carboline alkaloids from the stems of Picrasma quassioides.白皮树茎中的两个新β-咔啉生物碱。
Arch Pharm Res. 2018 May;41(5):513-518. doi: 10.1007/s12272-018-1034-2. Epub 2018 May 3.

引用本文的文献

1
(Hemsl.) Merr.: Ethnomedicinal, Phytochemistry, and Pharmacological Aspects.(赫姆斯利)梅里尔:民族药用、植物化学及药理学方面。
Plants (Basel). 2023 Dec 7;12(24):4094. doi: 10.3390/plants12244094.
2
Traditional Uses, Phytochemistry and Pharmacological Activities of Annonacae.番荔枝科植物的传统用途、植物化学和药理学活性。
Molecules. 2022 May 27;27(11):3462. doi: 10.3390/molecules27113462.
3
Novel total syntheses of oxoaporphine alkaloids enabled by mild Cu-catalyzed tandem oxidation/aromatization of 1-Bn-DHIQs.通过温和的铜催化1-Bn-DHIQs串联氧化/芳构化实现的氧代阿朴菲生物碱的新型全合成。

本文引用的文献

1
Chemical composition and antioxidant, antimicrobial, and larvicidal activities of the essential oils of Annona salzmannii and A. pickelii (Annonaceae).萨尔兹曼番荔枝和皮氏番荔枝(番荔枝科)精油的化学成分、抗氧化、抗菌和杀幼虫活性
Nat Prod Commun. 2011 Jun;6(6):907-12.
2
Natural products and Chagas' disease: a review of plant compounds studied for activity against Trypanosoma cruzi.天然产物与恰加斯病:抗克氏锥虫植物化合物的研究进展综述。
Nat Prod Rep. 2011 Apr;28(4):809-23. doi: 10.1039/c0np00069h. Epub 2011 Feb 3.
3
Flanking regions of monomorphic microsatellite loci provide a new source of data for plant species-level phylogenetics.
RSC Adv. 2018 Aug 14;8(51):28997-29007. doi: 10.1039/c8ra05338c.
4
Benzylated Dihydroflavones and Isoquinoline-Derived Alkaloids from the Bark of (Annonaceae) and Their Cytotoxicities.苯甲基二氢黄酮和小檗碱衍生生物碱来自(番荔枝科)树皮及其细胞毒性。
Molecules. 2021 Jun 18;26(12):3714. doi: 10.3390/molecules26123714.
5
Effects of a novel β-lapachone derivative on Trypanosoma cruzi: Parasite death involving apoptosis, autophagy and necrosis.一种新型β-拉帕醌衍生物对克氏锥虫的作用:涉及细胞凋亡、自噬和坏死的寄生虫死亡。
Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):207-219. doi: 10.1016/j.ijpddr.2016.10.003. Epub 2016 Oct 12.
6
Analgesic Potential of Essential Oils.精油的镇痛潜力。
Molecules. 2015 Dec 23;21(1):E20. doi: 10.3390/molecules21010020.
7
The influence of Brazilian plant extracts on Streptococcus mutans biofilm.巴西植物提取物对变形链球菌生物膜的影响。
J Appl Oral Sci. 2014 Sep-Oct;22(5):366-72. doi: 10.1590/1678-775720140085.
8
Cytotoxic Benzophenanthridine and Furoquinoline Alkaloids from Zanthoxylum buesgenii (Rutaceae).来自竹叶椒(芸香科)的细胞毒性苯并菲啶和呋喃喹啉生物碱。
Chem Cent J. 2014 Oct 21;8(1):61. doi: 10.1186/s13065-014-0061-4. eCollection 2014.
9
N-butyl-[1-(4-methoxy)phenyl-9H-β-carboline]-3-carboxamide prevents cytokinesis in Leishmania amazonensis.N-丁基-[1-(4-甲氧基)苯基-9H-β-咔啉]-3-甲酰胺可阻止亚马逊利什曼原虫的胞质分裂。
Antimicrob Agents Chemother. 2014 Dec;58(12):7112-20. doi: 10.1128/AAC.03340-14. Epub 2014 Sep 15.
10
Evaluation of the anti-inflammatory and antinociceptive effects of the essential oil from leaves of Xylopia laevigata in experimental models.光滑番荔枝叶精油在实验模型中的抗炎和镇痛作用评估
ScientificWorldJournal. 2014;2014:816450. doi: 10.1155/2014/816450. Epub 2014 Jul 3.
侧翼微卫星区域为植物种水平系统发育提供了新的数据源。
Mol Phylogenet Evol. 2009 Dec;53(3):726-33. doi: 10.1016/j.ympev.2009.07.024. Epub 2009 Jul 29.
4
7,7-Dimethylaporphine alkaloids from the stem of Guatteriopsis friesiana.来自弗氏瓜馥木茎中的7,7-二甲基阿朴啡生物碱。
J Nat Prod. 2009 Aug;72(8):1516-9. doi: 10.1021/np800788n.
5
Biological activity of 1,2,3,4-tetrahydro-beta-carboline-3-carboxamides against Trypanosoma cruzi.1,2,3,4-四氢-β-咔啉-3-甲酰胺对克氏锥虫的生物活性
Acta Trop. 2009 Apr;110(1):7-14. doi: 10.1016/j.actatropica.2008.11.008. Epub 2008 Nov 20.
6
Full NMR analysis of annomontine, methoxy- annomontine and N-hydroxyannomontine pyrimidine-beta-carboline alkaloids.
Magn Reson Chem. 2008 Jan;46(1):69-74. doi: 10.1002/mrc.2134.
7
A pyrimidine-beta-carboline and other alkaloids from Annona foetida with antileishmanial activity.一种来自恶臭番荔枝的具有抗利什曼原虫活性的嘧啶-β-咔啉及其他生物碱。
J Nat Prod. 2006 Feb;69(2):292-4. doi: 10.1021/np050422s.
8
Therapeutic activity and criterion of cure on mice experimentally infected with Trypanosoma cruzi.对实验感染克氏锥虫的小鼠的治疗活性和治愈标准
Rev Inst Med Trop Sao Paulo. 1962 Nov-Dec;4:389-96.
9
New ent-kaurane diterpenoids with anti-platelet aggregation activity from Annona squamosa.从番荔枝中分离得到的具有抗血小板聚集活性的新对映-贝壳杉烷二萜类化合物。
J Nat Prod. 2002 Oct;65(10):1462-7. doi: 10.1021/np020191e.
10
Effects of some beta-carboline alkaloids on intact Trypanosoma cruzi epimastigotes.
Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1999 Jan;122(1):27-31. doi: 10.1016/s0742-8413(98)10069-5.