• 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

吖啶酮生物碱对卡氏肺孢子虫的体外活性。

In vitro activities of acridone alkaloids against Pneumocystis carinii.

作者信息

Queener S F, Fujioka H, Nishiyama Y, Furukawa H, Bartlett M S, Smith J W

机构信息

Department of Pharmacology & Toxicology, Indiana University School of Medicine, Indianapolis 46202-5120.

出版信息

Antimicrob Agents Chemother. 1991 Feb;35(2):377-9. doi: 10.1128/AAC.35.2.377.

DOI:10.1128/AAC.35.2.377
PMID:2024971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC245010/
Abstract

Acridone alkaloids isolated from plants of the family Rutaceae have antiplasmodial activity in rodent models of malaria. Because a variety of antimalarial agents have also been shown to have activity against Pneumocystis carinii, we tested six of these alkaloids in an established culture model for P. carinii. Atalaphillinine and glycobismine A inhibited growth of cultured P. carinii at concentrations of 2.7 and 1.7 microM, respectively. This potency of effect is similar to that of chloroquine (3 microM) but somewhat less than that of primaquine (0.4 microM), which was previously evaluated in the same system.

摘要

从芸香科植物中分离出的吖啶酮生物碱在疟疾的啮齿动物模型中具有抗疟原虫活性。由于多种抗疟药也已显示出对卡氏肺孢子虫有活性,我们在已建立的卡氏肺孢子虫培养模型中测试了其中六种生物碱。阿塔拉菲林宁和甘氨双吖啶A分别在浓度为2.7微摩尔和1.7微摩尔时抑制培养的卡氏肺孢子虫的生长。这种作用效力与氯喹(3微摩尔)相似,但略低于先前在同一系统中评估的伯氨喹(0.4微摩尔)。

相似文献

1
In vitro activities of acridone alkaloids against Pneumocystis carinii.吖啶酮生物碱对卡氏肺孢子虫的体外活性。
Antimicrob Agents Chemother. 1991 Feb;35(2):377-9. doi: 10.1128/AAC.35.2.377.
2
Activities of new acridone alkaloid derivatives against Plasmodium yoelii in vitro.
Arzneimittelforschung. 1990 Sep;40(9):1026-9.
3
Bioactive acridone alkaloids from Swinglea glutinosa.来自粘滑番荔枝的生物活性吖啶酮生物碱。
J Nat Prod. 2001 Sep;64(9):1221-3. doi: 10.1021/np0005762.
4
In vitro and in vivo activities of atalaphillinine and related acridone alkaloids against rodent malaria.阿塔拉菲林宁及相关吖啶酮生物碱对啮齿类动物疟疾的体外和体内活性
Antimicrob Agents Chemother. 1989 Jan;33(1):6-9. doi: 10.1128/AAC.33.1.6.
5
In vitro activities of furoquinoline and acridone alkaloids against Plasmodium falciparum.呋喃喹啉和吖啶酮生物碱对恶性疟原虫的体外活性。
Antimicrob Agents Chemother. 1994 May;38(5):1169-71. doi: 10.1128/AAC.38.5.1169.
6
[Cytotoxicity of aspidospermane indole alkaloids with a modified tryptamine chain].[具有修饰色胺链的阿朴菲吲哚生物碱的细胞毒性]
J Nat Prod. 1995 Jul;58(7):1089-91. doi: 10.1021/np50121a018.
7
Molluscicidal acridone alkaloids from Angostura paniculata: isolation, structures, and synthesis.
J Nat Prod. 1992 Aug;55(8):1112-7. doi: 10.1021/np50086a012.
8
Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae) of southern Africa.来自非洲南部的杰氏特克莱木(芸香科:托达罗亚科)中的吖啶酮和呋喃喹啉生物碱。
Phytochemistry. 2007 Mar;68(5):663-7. doi: 10.1016/j.phytochem.2006.10.011. Epub 2006 Dec 15.
9
Isolation and in vitro antiplasmodial activities of alkaloids from Teclea trichocarpa: in vivo antimalarial activity and X-ray crystal structure of normelicopicine.毛果茶茱萸生物碱的分离及其体外抗疟活性:降新美洛匹辛的体内抗疟活性及X射线晶体结构
J Nat Prod. 2002 Jul;65(7):956-9. doi: 10.1021/np0106182.
10
Quinoline, quinazoline and acridone alkaloids.
Nat Prod Rep. 1997 Feb;14(1):11-20. doi: 10.1039/np9971400011.

引用本文的文献

1
Plant-derived chemicals as potential inhibitors of SARS-CoV-2 main protease (6LU7), a virtual screening study.植物源化学物质作为 SARS-CoV-2 主要蛋白酶(6LU7)抑制剂的潜力:一项虚拟筛选研究。
Phytother Res. 2021 Jun;35(6):3262-3274. doi: 10.1002/ptr.7041. Epub 2021 Mar 23.
2
Heterocycle-Fused Acridines.杂环稠合吖啶类化合物。
Adv Heterocycl Chem. 1997;70:89-161. doi: 10.1016/S0065-2725(08)60930-7. Epub 2008 Apr 25.
3
Identification of a class of sulfonamides highly active against dihydropteroate synthase form Toxoplasma gondii, Pneumocystis carinii, and Mycobacterium avium.鉴定出一类对刚地弓形虫、卡氏肺孢子虫和鸟分枝杆菌的二氢蝶酸合酶具有高活性的磺胺类药物。
Antimicrob Agents Chemother. 1996 Mar;40(3):727-33. doi: 10.1128/AAC.40.3.727.
4
Activity and mode of action of acridine compounds against Leishmania donovani.吖啶化合物对杜氏利什曼原虫的活性及作用方式
Antimicrob Agents Chemother. 1996 Mar;40(3):684-90. doi: 10.1128/AAC.40.3.684.
5
Evaluation of potent inhibitors of dihydrofolate reductase in a culture model for growth of Pneumocystis carinii.在卡氏肺孢子虫生长的培养模型中对二氢叶酸还原酶强效抑制剂的评估。
Antimicrob Agents Chemother. 1995 Nov;39(11):2436-41. doi: 10.1128/AAC.39.11.2436.
6
8-aminoquinolines effective against Pneumocystis carinii in vitro and in vivo.8-氨基喹啉在体外和体内对卡氏肺孢子虫有效。
Antimicrob Agents Chemother. 1993 Oct;37(10):2166-72. doi: 10.1128/AAC.37.10.2166.
7
In vitro activities of furoquinoline and acridone alkaloids against Plasmodium falciparum.呋喃喹啉和吖啶酮生物碱对恶性疟原虫的体外活性。
Antimicrob Agents Chemother. 1994 May;38(5):1169-71. doi: 10.1128/AAC.38.5.1169.
8
Molecular cloning and heterologous expression of acridone synthase from elicited Ruta graveolens L. cell suspension cultures.诱导的芸香细胞悬浮培养物中吖啶酮合酶的分子克隆及异源表达
Plant Mol Biol. 1995 Feb;27(4):681-92. doi: 10.1007/BF00020222.
9
Structure-activity and structure-selectivity studies on diaminoquinazolines and other inhibitors of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase.二氨基喹唑啉及其他卡氏肺孢子虫和刚地弓形虫二氢叶酸还原酶抑制剂的构效关系和构选关系研究
Antimicrob Agents Chemother. 1995 Jan;39(1):79-86. doi: 10.1128/AAC.39.1.79.

本文引用的文献

1
In vitro effects of antiprotozoan drugs and immune serum on Pneumocystis carinii.抗寄生虫药物和免疫血清对卡氏肺孢子虫的体外作用。
J Infect Dis. 1980 Jun;141(6):775-80. doi: 10.1093/infdis/141.6.775.
2
Alkaloids of Acronychia Baueri Schott I. Isolation of the alkaloids and a study of the antitumor and other biological properties of acronycine.
J Pharm Sci. 1966 Aug;55(8):758-68. doi: 10.1002/jps.2600550803.
3
Latent Pneumocystis infection of rats, relapse, and chemotherapy.大鼠的潜伏性肺孢子菌感染、复发及化疗
Lab Invest. 1966 Oct;15(10):1559-77.
4
Synthesis and biological activity of acronycine analogs.
J Med Chem. 1972 Mar;15(3):266-70. doi: 10.1021/jm00273a014.
5
Effects of the antineoplastic alkaloid acronycine on the ultrastructure and growth patterns of cultured cells.
Cancer Res. 1973 Oct;33(10):2320-9.
6
Antimicrobial susceptibility of Pneumocystis carinii in culture.卡氏肺孢子菌在培养中的药敏性。
Diagn Microbiol Infect Dis. 1985 Sep;3(5):381-7. doi: 10.1016/0732-8893(85)90076-8.
7
Activity of clindamycin with primaquine against Pneumocystis carinii in vitro and in vivo.克林霉素与伯氨喹联合应用对卡氏肺孢子虫的体内外活性
Antimicrob Agents Chemother. 1988 Jun;32(6):807-13. doi: 10.1128/AAC.32.6.807.
8
Quinoline, quinazoline, and acridone alkaloids.喹啉、喹唑啉和吖啶酮生物碱。
Nat Prod Rep. 1988 Jun;5(3):293-307. doi: 10.1039/np9880500293.
9
In vitro and in vivo activities of atalaphillinine and related acridone alkaloids against rodent malaria.阿塔拉菲林宁及相关吖啶酮生物碱对啮齿类动物疟疾的体外和体内活性
Antimicrob Agents Chemother. 1989 Jan;33(1):6-9. doi: 10.1128/AAC.33.1.6.
10
Pneumocystis carinii: improved models to study efficacy of drugs for treatment or prophylaxis of Pneumocystis pneumonia in the rat (Rattus spp.).卡氏肺孢子虫:用于研究大鼠(褐家鼠属)卡氏肺孢子虫肺炎治疗或预防药物疗效的改良模型。
Exp Parasitol. 1990 Jan;70(1):100-6. doi: 10.1016/0014-4894(90)90089-u.