• 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

可食用蘑菇中的艾杜烷倍半萜类化合物及其生物活性。

Illudane Sesquiterpenoids from Edible Mushroom and Their Bioactivities.

作者信息

Dai Quan, Zhang Fa-Lei, Du Jiao-Xian, Li Zheng-Hui, Feng Tao, Liu Ji-Kai

机构信息

School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, P. R. China.

The Modernization Engineering Technology Research Center of Ethnic Minority Medicine of Hubei Province, School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, P. R. China.

出版信息

ACS Omega. 2020 Aug 19;5(34):21961-21967. doi: 10.1021/acsomega.0c03314. eCollection 2020 Sep 1.

DOI:10.1021/acsomega.0c03314
PMID:32905428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7469647/
Abstract

To comprehensively understand the chemical constituents of the edible mushroom and their biological functions, a phytochemical separation of the cultural broth of led to the isolation of four new illudane sesquiterpenoids, agrocybins H-K (-), along with 10 known analogues (-). Compounds - were racemates of which and were further separated into single enantiomers as / and /. All new structures with absolute configurations were elucidated on the basis of an extensive spectroscopic analysis and quantum chemistry calculations. Compound possesses a new carbon skeleton that might be derived from the protoilludane backbone. Compounds , , , and show a certain degree of cytotoxicity to five human cancer cell lines. Compound shows a mild inhibitory effect on nitric oxide production with an IC value of 31.4 μM. It is concluded that is rich in illudin derivatives with potential bioactivity prospects, which would make a good material of medicine and food homology.

摘要

为全面了解食用菌的化学成分及其生物学功能,对其培养液进行植物化学分离,得到了四种新的伊利丹倍半萜类化合物,即农霉素H-K(-),以及10种已知类似物(-)。化合物-为外消旋体,其中和进一步拆分为单一对映体/和/。基于广泛的光谱分析和量子化学计算,阐明了所有具有绝对构型的新结构。化合物具有一种可能源自原伊利丹骨架的新碳骨架。化合物、、、和对五种人类癌细胞系表现出一定程度的细胞毒性。化合物对一氧化氮的产生具有轻度抑制作用,IC值为31.4μM。得出结论,富含具有潜在生物活性前景的伊利丹衍生物,这将使其成为药食同源的良好材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/5dbddc4ff7b5/ao0c03314_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/ba69f2d99411/ao0c03314_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/6c3f99898aca/ao0c03314_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/87369584d42c/ao0c03314_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/16418fc39e2a/ao0c03314_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/d6effea1d168/ao0c03314_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/5dbddc4ff7b5/ao0c03314_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/ba69f2d99411/ao0c03314_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/6c3f99898aca/ao0c03314_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/87369584d42c/ao0c03314_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/16418fc39e2a/ao0c03314_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/d6effea1d168/ao0c03314_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5be/7469647/5dbddc4ff7b5/ao0c03314_0006.jpg

相似文献

1
Illudane Sesquiterpenoids from Edible Mushroom and Their Bioactivities.可食用蘑菇中的艾杜烷倍半萜类化合物及其生物活性。
ACS Omega. 2020 Aug 19;5(34):21961-21967. doi: 10.1021/acsomega.0c03314. eCollection 2020 Sep 1.
2
Two new sesquiterpenoids from basidiomycete Agrocybe salicacola.来自担子菌杨树田头菇的两种新倍半萜类化合物。
J Asian Nat Prod Res. 2010 Jun;12(6):464-9. doi: 10.1080/10286020.2010.489822.
3
Illudin T, a new sesquiterpenoid from basidiomycete Agrocybe salicacola.
J Asian Nat Prod Res. 2011 May;13(5):430-3. doi: 10.1080/10286020.2011.566218.
4
Immunosuppressive Sesquiterpenoids from the Edible Mushroom .来自可食用蘑菇的免疫抑制倍半萜类化合物
J Fungi (Basel). 2021 Dec 8;7(12):1052. doi: 10.3390/jof7121052.
5
Isolation, Identification, and Bioactivity of Monoterpenoids and Sesquiterpenoids from the Mycelia of Edible Mushroom Pleurotus cornucopiae.食用蘑菇金针菇菌丝体中单萜和倍半萜的分离、鉴定及生物活性。
J Agric Food Chem. 2013 May 29;61(21):5122-9. doi: 10.1021/jf401612t. Epub 2013 May 16.
6
Characterization of Non-coding Regions in B Mating Loci of Agrocybe salicacola Groups: Target Sites for B Mating Type Identification.柳生田头菇组B交配位点非编码区的特征分析:B交配型鉴定的靶位点
Curr Microbiol. 2017 Jun;74(6):772-778. doi: 10.1007/s00284-017-1247-5. Epub 2017 Apr 10.
7
Characterization and NO inhibitory activities of chemical constituents from an edible plant Petasites tatewakianus.一种食用植物天蒜化学成分的鉴定及其对一氧化氮的抑制活性
J Agric Food Chem. 2014 Sep 24;62(38):9362-7. doi: 10.1021/jf5034224. Epub 2014 Sep 12.
8
Sesquiterpenes from cultures of the fungus Phellinus igniarius and their Cytotoxicities.火木层孔菌培养物中的倍半萜及其细胞毒性。
Fitoterapia. 2020 Jan;140:104415. doi: 10.1016/j.fitote.2019.104415. Epub 2019 Nov 5.
9
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.来源于内生真菌 Phomopsis sp. TJ507A 的原白头翁素、白头翁素和绵马烷倍半萜类化合物。
J Nat Prod. 2018 Jun 22;81(6):1311-1320. doi: 10.1021/acs.jnatprod.7b00889. Epub 2018 May 17.
10
Bioactive sesquiterpenoids from the flowers of Inula japonica.旋覆花中的生物活性倍半萜类化合物。
Phytochemistry. 2016 Sep;129:68-76. doi: 10.1016/j.phytochem.2016.07.008. Epub 2016 Jul 21.

引用本文的文献

1
Telomere-to-Telomere Haplotype-Resolved Genomes of Reveals Unique Genetic Features and Developmental Insights.端粒到端粒单倍型解析基因组揭示独特遗传特征与发育见解。 (你提供的原文“of Reveals”表述有误,推测可能是“of a Species Reveals”之类,这里按纠正后的大致意思翻译)
J Fungi (Basel). 2024 Aug 25;10(9):602. doi: 10.3390/jof10090602.
2
A comprehensive review of secondary metabolites from the genus : Biological activities and pharmacological implications.来自该属的次生代谢产物的全面综述:生物活性和药理学意义。
Mycology. 2023 Dec 25;15(2):162-179. doi: 10.1080/21501203.2023.2292994. eCollection 2024.
3
Sesquiterpenoids Specially Produced by Fungi: Structures, Biological Activities, Chemical and Biosynthesis (2015-2020).

本文引用的文献

1
Bovistol B, bovistol D and strossmayerin: Sesquiterpene metabolites from the culture filtrate of the basidiomycete Coprinopsis strossmayeri.博维他汀 B、博维他汀 D 和斯特罗迈耶林:担子菌Coprinopsis strossmayeri 发酵滤液中的倍半萜代谢物。
PLoS One. 2020 Apr 6;15(4):e0229925. doi: 10.1371/journal.pone.0229925. eCollection 2020.
2
Monoterpenoid indole alkaloids from the bark of Melodinus henryi.从密花轮环藤的树皮中分离得到的单萜吲哚生物碱。
Fitoterapia. 2019 Oct;138:104354. doi: 10.1016/j.fitote.2019.104354. Epub 2019 Aug 30.
3
New terpenoids from the fermentation broth of the edible mushroom .
真菌特有的倍半萜类化合物:结构、生物活性、化学与生物合成(2015 - 2020年)
J Fungi (Basel). 2021 Nov 30;7(12):1026. doi: 10.3390/jof7121026.
可食用蘑菇发酵液中的新型萜类化合物。
Beilstein J Org Chem. 2019 Apr 30;15:1000-1007. doi: 10.3762/bjoc.15.98. eCollection 2019.
4
Cytotoxic illudalane sesquiterpenes from the wood-decay fungus Granulobasidium vellereum (Ellis & Cragin) Jülich.来自木材腐朽真菌绒毛粒皮菌(Granulobasidium vellereum (Ellis & Cragin) Jülich)的细胞毒性伊利达内酯倍半萜。
Molecules. 2014 Sep 9;19(9):14195-203. doi: 10.3390/molecules190914195.
5
SpecDis: quantifying the comparison of calculated and experimental electronic circular dichroism spectra.SpecDis:计算和实验电子圆二色光谱的比较量化。
Chirality. 2013 Apr;25(4):243-9. doi: 10.1002/chir.22138.
6
Sterostreins F-O, illudalanes and norilludalanes from cultures of the Basidiomycete Stereum ostrea BCC 22955.Sterostreins F-O、来源于担子菌纲 Stereum ostrea BCC 22955 培养物的 illudalanes 和 norilludalanes。
Phytochemistry. 2012 Jul;79:116-20. doi: 10.1016/j.phytochem.2012.04.009. Epub 2012 May 15.
7
Chemistry and biology of acylfulvenes: sesquiterpene-derived antitumor agents.酰基富烯的化学与生物学:倍半萜衍生的抗肿瘤药物
Chem Rev. 2012 Jun 13;112(6):3578-610. doi: 10.1021/cr2001367. Epub 2012 Apr 6.
8
Illudin T, a new sesquiterpenoid from basidiomycete Agrocybe salicacola.
J Asian Nat Prod Res. 2011 May;13(5):430-3. doi: 10.1080/10286020.2011.566218.
9
Anticancer active illudins: recent developments of a potent alkylating compound class.抗癌活性伊鲁丁:一种有效烷基化化合物类别的最新进展。
Curr Med Chem. 2011;18(6):790-807. doi: 10.2174/092986711794927766.
10
Antineoplastic agents 582. Part 1: Isolation and structure of a cyclobutane-type sesquiterpene cancer cell growth inhibitor from Coprinus cinereus (Coprinaceae).抗肿瘤药物 582. 第 1 部分:从灰盖鬼伞(鬼笔科)中分离出一种具有环丁烷型倍半萜结构的癌细胞生长抑制剂
Bioorg Med Chem. 2010 Jul 15;18(14):4879-83. doi: 10.1016/j.bmc.2010.06.023. Epub 2010 Jun 12.