• 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

石蒜科的化学和生物活性。

The chemistry and biological activity of the Hyacinthaceae.

机构信息

Natural Products Research Group, Department of Chemistry, University of Surrey, Guildford, GU2 7XH, United Kingdom.

出版信息

Nat Prod Rep. 2013 Sep;30(9):1165-210. doi: 10.1039/c3np70008a. Epub 2013 Jul 29.

DOI:10.1039/c3np70008a
PMID:23892453
Abstract

The Hyacinthaceae (sensu APGII), with approximately 900 species in about 70 genera, can be divided into three main subfamilies, the Hyacinthoideae, the Urgineoideae and the Ornithogaloideae, with a small fourth subfamily the Oziroëoideae, restricted to South America. The plants included in this family have long been used in traditional medicine for a wide range of medicinal applications. This, together with some significant toxicity to livestock has led to the chemical composition of many of the species being investigated. The compounds found are, for the most part, subfamily-restricted, with homoisoflavanones and spirocyclic nortriterpenoids characterising the Hyacinthoideae, bufadienolides characterising the Urgineoideae, and cardenolides and steroidal glycosides characterising the Ornithogaloideae. The phytochemical profiles of 38 genera of the Hyacinthaceae will be discussed as well as any biological activity associated with both crude extracts and compounds isolated. The Hyacinthaceae of southern Africa were last reviewed in 2000 (T. S. Pohl, N. R. Crouch and D. A. Mulholland, Curr. Org. Chem., 2000, 4, 1287-1324; ref. 1); the current contribution considers the family at a global level.

摘要

风信子科(APGII 系统)约有 900 种,分属 70 余属,可分为三个主要的亚科,即风信子亚科、喇叭兰亚科和蓝星花亚科,还有一个小的第四亚科,即奥孜罗埃亚科,仅限于南美洲。该科植物长期以来一直被用于传统医学,具有广泛的药用用途。这一点,再加上对牲畜的一些显著毒性,导致许多物种的化学成分受到了研究。发现的化合物在大多数情况下是亚科特有的,同型异黄酮和螺环三萜类化合物是风信子亚科的特征,蟾蜍毒是喇叭兰亚科的特征,而强心苷和甾体糖苷是蓝星花亚科的特征。本文将讨论 38 个风信子科属的植物化学特征,以及与粗提取物和分离化合物相关的任何生物活性。2000 年对南非的风信子科植物进行了最后一次综述(T. S. Pohl、N. R. Crouch 和 D. A. Mulholland,Curr. Org. Chem.,2000,4,1287-1324;参考文献 1);本研究在全球范围内对该科进行了探讨。

相似文献

1
The chemistry and biological activity of the Hyacinthaceae.石蒜科的化学和生物活性。
Nat Prod Rep. 2013 Sep;30(9):1165-210. doi: 10.1039/c3np70008a. Epub 2013 Jul 29.
2
Bufadienolides from the southern African Drimia depressa (Hyacinthaceae: Urgineoideae).来自南非矮仙茅(风信子科:仙茅亚科)的蟾蜍二烯羟酸内酯
Phytochemistry. 2007 Jul;68(13):1731-4. doi: 10.1016/j.phytochem.2007.04.003. Epub 2007 May 18.
3
Bufadienolides from Drimia macrocentra and Urginea riparia (Hyacinthaceae: Urgineoideae).来自大中心绵枣儿和河岸绵枣儿(风信子科:绵枣儿亚科)的蟾蜍二烯羟酸内酯
Phytochemistry. 2007 Oct;68(19):2415-9. doi: 10.1016/j.phytochem.2007.05.023. Epub 2007 Jul 2.
4
Phytochemical Investigations of Three Rhodocodon (Hyacinthaceae Sensu APG II) Species.三种紫堇科(APG II系统下的风信子科)植物的植物化学研究
J Nat Prod. 2017 Jan 27;80(1):30-37. doi: 10.1021/acs.jnatprod.6b00240. Epub 2017 Jan 4.
5
Homoisoflavanones from Pseudoprospero firmifolium of the monotypic tribe Pseudoprospereae (Hyacinthaceae: Hyacinthoideae).单型族假普罗丝草族(风信子科:风信子亚科)假硬叶假普罗丝草中的高异黄酮类化合物。
Phytochemistry. 2007 Nov-Dec;68(22-24):2753-6. doi: 10.1016/j.phytochem.2007.08.005. Epub 2007 Sep 19.
6
COX-2 inhibitory activity of homoisoflavanones and xanthones from the bulbs of the Southern African Ledebouria socialis and Ledebouria ovatifolia (Hyacinthaceae: Hyacinthoideae).南非 Ledebouria socialis 和 Ledebouria ovatifolia(天门冬科:萱草科)鳞茎中的异黄烷酮和酮类化合物对 COX-2 的抑制活性。
Phytochemistry. 2013 Nov;95:284-90. doi: 10.1016/j.phytochem.2013.06.024. Epub 2013 Jul 13.
7
Out of Africa: Miocene dispersal, vicariance, and extinction within Hyacinthaceae subfamily Urgineoideae.走出非洲:Hyacinthaceae 亚科 Urgineoideae 中的中新世扩散、地理隔离和灭绝。
J Integr Plant Biol. 2013 Oct;55(10):950-64. doi: 10.1111/jipb.12065. Epub 2013 Aug 30.
8
Bufadienolides from bulbs of Urginea lydenburgensis (Hyacinthaceae: Urgineoideae).来自莱登堡地百合(风信子科:绵枣儿亚科)鳞茎的蟾蜍二烯羟酸内酯
Phytochemistry. 2006 Oct;67(19):2140-5. doi: 10.1016/j.phytochem.2006.05.009. Epub 2006 Jul 10.
9
Bufadienolides from Drimia robusta and Urginea epigea (Hyacinthaceae).来自粗壮海葱和地中海绵枣儿(风信子科)的蟾蜍二烯羟酸内酯
Phytochemistry. 2004 Dec;65(23):3069-73. doi: 10.1016/j.phytochem.2004.08.051.
10
Vascular myorelaxing activity of isolates from South African Hyacinthaceae partly mediated by activation of soluble guanylyl cyclase in rat aortic ring preparations.南非风信子科植物分离物的血管肌松弛活性在大鼠主动脉环标本中部分由可溶性鸟苷酸环化酶的激活介导。
J Pharm Pharmacol. 2008 Apr;60(4):489-97. doi: 10.1211/jpp.60.4.0012.

引用本文的文献

1
Integration Viewpoint Using UHPLC-MS/MS, In Silico Analysis, Network Pharmacology, and In Vitro Analysis to Evaluate the Bio-Potential of Extracts.运用超高效液相色谱-串联质谱法(UHPLC-MS/MS)、计算机模拟分析、网络药理学和体外分析的整合观点来评估提取物的生物潜力。
Molecules. 2025 Jul 4;30(13):2855. doi: 10.3390/molecules30132855.
2
Cyclic Imines and Their Salts as Universal Precursors in the Synthesis of Nitrogen-Containing Alkaloids.环状亚胺及其盐类作为含氮生物碱合成中的通用前体。
Int J Mol Sci. 2024 Dec 31;26(1):288. doi: 10.3390/ijms26010288.
3
Exploring the Antiangiogenic and Anti-Inflammatory Potential of Homoisoflavonoids: Target Identification Using Biotin Probes.
探索异黄酮类化合物的抗血管生成和抗炎潜力:使用生物素探针进行的靶标鉴定。
Biomolecules. 2024 Jun 30;14(7):785. doi: 10.3390/biom14070785.
4
The Bioactivity and Phytochemicals of (), a Plant of Multiple Pharmacological Activities.具有多种药理活性的植物()的生物活性与植物化学物质
Int J Mol Sci. 2024 Feb 23;25(5):2592. doi: 10.3390/ijms25052592.
5
Potential pharmacokinetic interactions with concurrent use of herbal medicines and a ritonavir-boosted COVID-19 protease inhibitor in low and middle-income countries.在低收入和中等收入国家,草药与利托那韦增强型COVID-19蛋白酶抑制剂同时使用时的潜在药代动力学相互作用。
Front Pharmacol. 2023 Jul 12;14:1210579. doi: 10.3389/fphar.2023.1210579. eCollection 2023.
6
Comparative Cytogenetics and Fluorescent Chromosome Banding in Five Indian Species of Medik.五种印度药用植物的比较细胞遗传学与荧光染色体显带分析
Plants (Basel). 2023 Jul 3;12(13):2534. doi: 10.3390/plants12132534.
7
Acaricidal Activity of Bufadienolides Isolated from against and Structural Elucidation of Arenobufagin-3--L-rhamnopyranoside.从 中分离得到的蟾蜍二烯醇类化合物对 的杀螨活性及沙蟾毒精-3--L-鼠李吡喃糖苷的结构解析
Plants (Basel). 2022 Jun 21;11(13):1629. doi: 10.3390/plants11131629.
8
Bulbous Plants : "A Thin Line between Poisonous and Healing Compounds" with Biological Activities.球根植物:“有毒化合物与具有生物活性的治疗性化合物之间的微妙界限”
Pharmaceutics. 2021 Sep 1;13(9):1385. doi: 10.3390/pharmaceutics13091385.
9
Total Synthesis of Naturally Occurring 5,7,8-Trioxygenated Homoisoflavonoids.天然存在的5,7,8-三氧化异黄酮类化合物的全合成
ACS Omega. 2020 May 6;5(19):11043-11057. doi: 10.1021/acsomega.0c00932. eCollection 2020 May 19.
10
Sulfadiazine Masquerading as a Natural Product from (Scilloideae).磺胺哒嗪伪装成来自(石蒜科)的天然产物。
J Nat Prod. 2020 Apr 24;83(4):1305-1308. doi: 10.1021/acs.jnatprod.0c00163. Epub 2020 Mar 25.