• 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

从真菌 - 衍生的 sp. PQJ-1 中分离得到的细胞毒性吲哚二萜。

Cytotoxic Indole Diterpenoids from a -Derived Fungus sp. PQJ-1.

机构信息

Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, China.

Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, China.

出版信息

Molecules. 2023 Oct 10;28(20):7003. doi: 10.3390/molecules28207003.

DOI:10.3390/molecules28207003
PMID:37894482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10609460/
Abstract

Two new indole diterpene derivatives, 5-hydroxy--aflatrem () and 14-hydroxy--aflatrem (), along with one known analogue, 14-(,-dimethl--valyloxy)paspalinine (), were isolated from the fermentation broth of the fungus sp. PQJ-1 derived from . The structures of the new compounds were elucidated from spectroscopic data and ECD spectroscopic analyses. All the compounds (-) were evaluated for their cytotoxicity against A549, Hela, Hep G2, and MCF-7 cell lines. Compounds and exhibited selective inhibition against Hela cells. Further studies showed that significantly induced apoptosis and suppressed migration and invasion in Hela cells. Moreover, could up-regulate pro-apoptotic genes BAX and Caspase-3 and down-regulate anti-apoptotic genes Bcl-xL and XIXP.

摘要

从采自 的真菌 sp. PQJ-1 的发酵液中分离得到了两个新的吲哚二萜衍生物,5-羟基--黄曲霉毒素 () 和 14-羟基--黄曲霉毒素 (),以及一个已知类似物 14-(-,-二甲- -缬氨酰氧基)巴卡丁 (). 新化合物的结构通过光谱数据和 ECD 光谱分析阐明。所有化合物 (-) 都对 A549、Hela、Hep G2 和 MCF-7 细胞系进行了细胞毒性评估。化合物 和 对 Hela 细胞表现出选择性抑制作用。进一步的研究表明, 能显著诱导 Hela 细胞凋亡,并抑制其迁移和侵袭。此外, 可上调促凋亡基因 BAX 和 Caspase-3,下调抗凋亡基因 Bcl-xL 和 XIXP。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/0340bebf270a/molecules-28-07003-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/352102bfbe75/molecules-28-07003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/9d52661cbfa0/molecules-28-07003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/0709dddff513/molecules-28-07003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/8ca9e7b89d15/molecules-28-07003-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/73bd154e812a/molecules-28-07003-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/0340bebf270a/molecules-28-07003-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/352102bfbe75/molecules-28-07003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/9d52661cbfa0/molecules-28-07003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/0709dddff513/molecules-28-07003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/8ca9e7b89d15/molecules-28-07003-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/73bd154e812a/molecules-28-07003-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ca1/10609460/0340bebf270a/molecules-28-07003-g006.jpg

相似文献

1
Cytotoxic Indole Diterpenoids from a -Derived Fungus sp. PQJ-1.从真菌 - 衍生的 sp. PQJ-1 中分离得到的细胞毒性吲哚二萜。
Molecules. 2023 Oct 10;28(20):7003. doi: 10.3390/molecules28207003.
2
Two new lactam derivatives from a derived fungus PQJ-2.从真菌 PQJ-2 中分离得到的两个新的内酰胺衍生物。
Nat Prod Res. 2024 Jan-Feb;38(3):372-378. doi: 10.1080/14786419.2022.2122964. Epub 2022 Sep 16.
3
Penicindopene A, a new indole diterpene from the deep-sea fungus sp. YPCMAC1.Penicindopene A,一种新型吲哚二萜类化合物,来源于深海真菌 YPCMAC1。
Nat Prod Res. 2019 Oct;33(20):2988-2994. doi: 10.1080/14786419.2018.1514402. Epub 2018 Oct 1.
4
Cytotoxic Indole-Diterpenoids from the Marine-Derived Fungus sp. KFD28.海洋来源真菌 sp. KFD28 中的细胞毒吲哚二萜
Mar Drugs. 2021 Oct 28;19(11):613. doi: 10.3390/md19110613.
5
Indole diterpenoids and isocoumarin from the fungus, Aspergillus flavus, isolated from the prawn, Penaeus vannamei.从凡纳滨对虾中分离出的黄曲霉真菌中的吲哚二萜类化合物和异香豆素。
Mar Drugs. 2014 Jun 30;12(7):3970-81. doi: 10.3390/md12073970.
6
Diverse indole-diterpenoids with protein tyrosine phosphatase 1B inhibitory activities from the marine coral-derived fungus Aspergillus sp. ZF-104.海洋珊瑚来源真菌 Aspergillus sp. ZF-104 中具有蛋白酪氨酸磷酸酶 1B 抑制活性的多样吲哚二萜。
Phytochemistry. 2023 Dec;216:113888. doi: 10.1016/j.phytochem.2023.113888. Epub 2023 Oct 14.
7
Asperindoles A⁻D and a -Terphenyl Derivative from the Ascidian-Derived Fungus sp. KMM 4676.海绵来源真菌 KMM 4676 中分离得到的asperindoles A⁻D 和 a-三联苯衍生物
Mar Drugs. 2018 Jul 9;16(7):232. doi: 10.3390/md16070232.
8
20--Isopimarane and isopimarane diterpenoids produced by sp. WT03.松烷和松烷二萜类化合物由 WT03 产生。
Org Biomol Chem. 2023 Mar 1;21(9):1895-1902. doi: 10.1039/d3ob00005b.
9
Three new indole diterpenoids from KKU-CT2.KKU-CT2 中三种新的吲哚二萜
Nat Prod Res. 2022 Oct;36(19):4973-4981. doi: 10.1080/14786419.2021.1914613. Epub 2021 Jun 6.
10
Tetranorlabdane Diterpenoids from the Deep Sea Sediment-Derived Fungus Aspergillus wentii SD-310.源自深海沉积物真菌文氏曲霉SD-310的四环降蒈二萜类化合物
Planta Med. 2016 Jun;82(9-10):877-81. doi: 10.1055/s-0042-102965. Epub 2016 Jun 3.

引用本文的文献

1
Newly isolated terpenoids (covering 2019-2024) from Aspergillus species and their potential for the discovery of novel antimicrobials.从曲霉属物种中最新分离出的萜类化合物(涵盖2019年至2024年)及其发现新型抗菌剂的潜力。
Nat Prod Bioprospect. 2025 Mar 18;15(1):19. doi: 10.1007/s13659-025-00501-2.

本文引用的文献

1
Four Undescribed Pyranones from the -Derived Endophytic Fungi sp. FAE17.从内生真菌 sp. FAE17 中分离得到的四个未描述的吡喃酮。
Molecules. 2023 Jul 13;28(14):5388. doi: 10.3390/molecules28145388.
2
Hainanxylogranolides A-F: New Limonoids isolated from the seeds of Hainan mangrove plant Xylocarpus granatum.海南木榄烷型新倍半萜:从海南红树林植物木榄种子中分离得到的新倍半萜。
Fitoterapia. 2023 Mar;165:105407. doi: 10.1016/j.fitote.2022.105407. Epub 2022 Dec 26.
3
Targeting CRL4 suppresses chemoresistant ovarian cancer growth by inducing mitophagy.
靶向 CRL4 诱导自噬抑制耐药性卵巢癌细胞生长。
Signal Transduct Target Ther. 2022 Dec 9;7(1):388. doi: 10.1038/s41392-022-01253-y.
4
The Biosynthesis Related Enzyme, Structure Diversity and Bioactivity Abundance of Indole-Diterpenes: A Review.吲哚二萜类的生物合成相关酶、结构多样性和生物活性丰度:综述。
Molecules. 2022 Oct 13;27(20):6870. doi: 10.3390/molecules27206870.
5
Two new lactam derivatives from a derived fungus PQJ-2.从真菌 PQJ-2 中分离得到的两个新的内酰胺衍生物。
Nat Prod Res. 2024 Jan-Feb;38(3):372-378. doi: 10.1080/14786419.2022.2122964. Epub 2022 Sep 16.
6
7-Methoxy-13-dehydroxypaxilline: New indole diterpenoid from an endophytic fungus sp. Nb 19.7-甲氧基-13-去羟基鬼笔环肽:来自内生真菌Nb 19的新型吲哚二萜类化合物。
Nat Prod Res. 2024 Jan-Feb;38(1):103-111. doi: 10.1080/14786419.2022.2107639. Epub 2022 Aug 5.
7
Oxalierpenes A and B, Unusual Indole-Diterpenoid Derivatives with Antiviral Activity from a Marine-Derived Strain of the Fungus .Oxalierpenes A 和 B,一种具有抗病毒活性的新型吲哚二萜衍生物,来源于海洋来源真菌的一株真菌。
J Nat Prod. 2022 Jul 22;85(7):1880-1885. doi: 10.1021/acs.jnatprod.2c00322. Epub 2022 Jun 21.
8
Anti-IAV indole-diterpenoids from the marine-derived fungus .来自海洋真菌的抗甲型流感病毒吲哚二萜类化合物
Nat Prod Res. 2023 Feb;37(4):586-591. doi: 10.1080/14786419.2022.2078820. Epub 2022 May 24.
9
Cytotoxic Nitrobenzoyl Sesquiterpenoids from an Antarctica Sponge-Derived .源自南极海绵的细胞毒性硝基苯甲酰倍半萜类化合物
J Nat Prod. 2022 Apr 22;85(4):987-996. doi: 10.1021/acs.jnatprod.1c01118. Epub 2022 Apr 5.
10
Synthesis of 8-Fluoroneocryptolepine and Evaluation for Cytotoxic Activity against AGS Cancer Cells.8-氟新隐丹参酮的合成及其对 AGS 癌细胞的细胞毒性评价。
J Nat Prod. 2022 Apr 22;85(4):963-971. doi: 10.1021/acs.jnatprod.1c01078. Epub 2022 Feb 22.