T. Khosnutdinova, N. Gemejiyeva, Zhanat Karzhaubekova, N. Sultanova
{"title":"Coumarins of genus Ferula L. (Apiaceae Lindl.)","authors":"T. Khosnutdinova, N. Gemejiyeva, Zhanat Karzhaubekova, N. Sultanova","doi":"10.18321/ectj1494","DOIUrl":null,"url":null,"abstract":"The biologically active coumarins from Ferula L. species of the family Apiaceae Lindl. for the period 1970 to 2022 have been reviewed. The phytochemical investigation of different parts of Ferula L., including gum resin, leaves, fruits, seeds, roots, rhizomes, and resins led to the separation of different types of coumarins. Nearly 185 coumarins were isolated from 35 species of Ferula L. growing in different countries. Coumarins are represented mainly by umbelliferone (7-O-hydroxycoumarin) derivatives substituted in the C-7 position of aglycone, furanocoumarins and metabolites have terpene fragments, esters and glycosides. Umbelliferon is found as a taxon for the genus Ferula L. Some «unusual» metabolites have a furan fragment attached to the pyrone ring. Coumarins are of the psoralen type, containing a furan ring in the C-6 and C-7 positions of the primary skeleton. The rare coumarins with terpene fragments (hemiterpene, monoterpen, sesquiterpene) were reported. The biological activities of some extracts and individual metabolites such as antiinflammatory, cytotoxicity, antibacterial, antileishmanial, antiviral, antigenotoxic, antitumor, anticoagulant, antioxidant, antimycobacterial, inhibition a-glucosidase, antileishmanial were found.","PeriodicalId":11795,"journal":{"name":"Eurasian Chemico-Technological Journal","volume":" ","pages":""},"PeriodicalIF":0.5000,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Eurasian Chemico-Technological Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18321/ectj1494","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
蜂科阿魏属植物中具有生物活性的香豆素。对1970年至2022年期间进行了审查。通过对阿魏树胶树脂、叶片、果实、种子、根、根茎和树脂等不同部位的植物化学研究,分离出了不同类型的香豆素。从分布在不同国家的35种阿魏植物中分离到近185种香豆素。香豆素主要以伞形素(7- o -羟基香豆素)衍生物取代苷元C-7位,呋喃香豆素及其代谢产物有萜烯片段、酯类和苷类。umbellliferon被发现为阿魏属的一个分类群。一些“不寻常的”代谢物有一个呋喃片段附在吡酮环上。香豆素是补骨脂素类型,在主骨架的C-6和C-7位置含有呋喃环。报道了含有萜烯片段的罕见香豆素(半萜、单萜、倍半萜)。发现部分提取物和个别代谢产物具有抗炎、细胞毒、抗菌、抗利什曼原虫、抗病毒、抗基因毒性、抗肿瘤、抗凝血、抗氧化、抗真菌、抑制a-葡萄糖苷酶、抗利什曼原虫等生物活性。
The biologically active coumarins from Ferula L. species of the family Apiaceae Lindl. for the period 1970 to 2022 have been reviewed. The phytochemical investigation of different parts of Ferula L., including gum resin, leaves, fruits, seeds, roots, rhizomes, and resins led to the separation of different types of coumarins. Nearly 185 coumarins were isolated from 35 species of Ferula L. growing in different countries. Coumarins are represented mainly by umbelliferone (7-O-hydroxycoumarin) derivatives substituted in the C-7 position of aglycone, furanocoumarins and metabolites have terpene fragments, esters and glycosides. Umbelliferon is found as a taxon for the genus Ferula L. Some «unusual» metabolites have a furan fragment attached to the pyrone ring. Coumarins are of the psoralen type, containing a furan ring in the C-6 and C-7 positions of the primary skeleton. The rare coumarins with terpene fragments (hemiterpene, monoterpen, sesquiterpene) were reported. The biological activities of some extracts and individual metabolites such as antiinflammatory, cytotoxicity, antibacterial, antileishmanial, antiviral, antigenotoxic, antitumor, anticoagulant, antioxidant, antimycobacterial, inhibition a-glucosidase, antileishmanial were found.
期刊介绍:
The journal is designed for publication of experimental and theoretical investigation results in the field of chemistry and chemical technology. Among priority fields that emphasized by chemical science are as follows: advanced materials and chemical technologies, current issues of organic synthesis and chemistry of natural compounds, physical chemistry, chemical physics, electro-photo-radiative-plasma chemistry, colloids, nanotechnologies, catalysis and surface-active materials, polymers, biochemistry.