• 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

海洋吡咯生物碱。

Marine Pyrrole Alkaloids.

机构信息

Department of Chemistry, Organic Chemistry Section, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany.

出版信息

Mar Drugs. 2021 Sep 10;19(9):514. doi: 10.3390/md19090514.

DOI:10.3390/md19090514
PMID:34564176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8471394/
Abstract

Nitrogen heterocycles are essential parts of the chemical machinery of life and often reveal intriguing structures. They are not only widespread in terrestrial habitats but can also frequently be found as natural products in the marine environment. This review highlights the important class of marine pyrrole alkaloids, well-known for their diverse biological activities. A broad overview of the marine pyrrole alkaloids with a focus on their isolation, biological activities, chemical synthesis, and derivatization covering the decade from 2010 to 2020 is provided. With relevant structural subclasses categorized, this review shall provide a clear and timely synopsis of this area.

摘要

氮杂环是生命化学机制的重要组成部分,常常呈现出引人入胜的结构。它们不仅广泛存在于陆地生境中,而且还经常作为海洋环境中的天然产物出现。本综述重点介绍了海洋吡咯生物碱这一重要的化合物类别,它们以多样的生物活性而闻名。本文提供了 2010 年至 2020 年这十年来海洋吡咯生物碱的广泛概述,包括它们的分离、生物活性、化学合成和衍生化,重点介绍了其结构分类。通过对相关结构亚类进行分类,本文将对这一领域进行清晰及时的综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/95ccc576aa43/marinedrugs-19-00514-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/e9205ca8bd46/marinedrugs-19-00514-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/d7f5f112dc44/marinedrugs-19-00514-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6bbb184f4f47/marinedrugs-19-00514-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/89db00359bf0/marinedrugs-19-00514-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f793681be2a1/marinedrugs-19-00514-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/32bbbdc441bb/marinedrugs-19-00514-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/7e9f9bf72f6b/marinedrugs-19-00514-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/e61aa881aab8/marinedrugs-19-00514-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/78f943f436d0/marinedrugs-19-00514-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/2eddd0126b6a/marinedrugs-19-00514-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/9b35e2f9f68d/marinedrugs-19-00514-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/93338a6b9fe6/marinedrugs-19-00514-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/972db12eee48/marinedrugs-19-00514-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/3528ad026939/marinedrugs-19-00514-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/0cd9494a8677/marinedrugs-19-00514-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/2f0b0e55f76d/marinedrugs-19-00514-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/32b7cb50ac56/marinedrugs-19-00514-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/5decd3efd710/marinedrugs-19-00514-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/eda1b9d6b76f/marinedrugs-19-00514-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/fe7ca7848d11/marinedrugs-19-00514-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/37d182f1affb/marinedrugs-19-00514-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/ddb2f3437d58/marinedrugs-19-00514-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6056dd999611/marinedrugs-19-00514-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/41583d0f1065/marinedrugs-19-00514-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/3e9c80d5fb94/marinedrugs-19-00514-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/1973f4b0dc9f/marinedrugs-19-00514-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/602252844ffe/marinedrugs-19-00514-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6a0e00b29a6f/marinedrugs-19-00514-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/b8dfdba50496/marinedrugs-19-00514-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f78a707b686a/marinedrugs-19-00514-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f75709179130/marinedrugs-19-00514-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6ddb158c4e3a/marinedrugs-19-00514-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/0cf8526c6a7e/marinedrugs-19-00514-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/00603c158729/marinedrugs-19-00514-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/711545022821/marinedrugs-19-00514-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6fefc00f0654/marinedrugs-19-00514-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/ef8249498123/marinedrugs-19-00514-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/7e0266596b13/marinedrugs-19-00514-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/1ac551e6541d/marinedrugs-19-00514-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/acddab1a168d/marinedrugs-19-00514-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/8fa4f199c8a4/marinedrugs-19-00514-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/fe78a2f1b079/marinedrugs-19-00514-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/03866438c273/marinedrugs-19-00514-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/95ccc576aa43/marinedrugs-19-00514-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/e9205ca8bd46/marinedrugs-19-00514-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/d7f5f112dc44/marinedrugs-19-00514-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6bbb184f4f47/marinedrugs-19-00514-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/89db00359bf0/marinedrugs-19-00514-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f793681be2a1/marinedrugs-19-00514-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/32bbbdc441bb/marinedrugs-19-00514-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/7e9f9bf72f6b/marinedrugs-19-00514-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/e61aa881aab8/marinedrugs-19-00514-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/78f943f436d0/marinedrugs-19-00514-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/2eddd0126b6a/marinedrugs-19-00514-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/9b35e2f9f68d/marinedrugs-19-00514-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/93338a6b9fe6/marinedrugs-19-00514-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/972db12eee48/marinedrugs-19-00514-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/3528ad026939/marinedrugs-19-00514-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/0cd9494a8677/marinedrugs-19-00514-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/2f0b0e55f76d/marinedrugs-19-00514-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/32b7cb50ac56/marinedrugs-19-00514-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/5decd3efd710/marinedrugs-19-00514-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/eda1b9d6b76f/marinedrugs-19-00514-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/fe7ca7848d11/marinedrugs-19-00514-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/37d182f1affb/marinedrugs-19-00514-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/ddb2f3437d58/marinedrugs-19-00514-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6056dd999611/marinedrugs-19-00514-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/41583d0f1065/marinedrugs-19-00514-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/3e9c80d5fb94/marinedrugs-19-00514-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/1973f4b0dc9f/marinedrugs-19-00514-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/602252844ffe/marinedrugs-19-00514-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6a0e00b29a6f/marinedrugs-19-00514-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/b8dfdba50496/marinedrugs-19-00514-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f78a707b686a/marinedrugs-19-00514-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/f75709179130/marinedrugs-19-00514-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6ddb158c4e3a/marinedrugs-19-00514-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/0cf8526c6a7e/marinedrugs-19-00514-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/00603c158729/marinedrugs-19-00514-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/711545022821/marinedrugs-19-00514-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/6fefc00f0654/marinedrugs-19-00514-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/ef8249498123/marinedrugs-19-00514-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/7e0266596b13/marinedrugs-19-00514-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/1ac551e6541d/marinedrugs-19-00514-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/acddab1a168d/marinedrugs-19-00514-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/8fa4f199c8a4/marinedrugs-19-00514-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/fe78a2f1b079/marinedrugs-19-00514-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/03866438c273/marinedrugs-19-00514-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0595/8471394/95ccc576aa43/marinedrugs-19-00514-g039.jpg

相似文献

1
Marine Pyrrole Alkaloids.海洋吡咯生物碱。
Mar Drugs. 2021 Sep 10;19(9):514. doi: 10.3390/md19090514.
2
Antibacterial and Antibiofilm Potentials of Marine Pyrrole-2-Aminoimidazole Alkaloids and their Synthetic Analogs.海洋吡咯-2-氨基咪唑生物碱及其合成类似物的抗菌和抗生物膜潜力。
Mini Rev Med Chem. 2018;18(19):1640-1658. doi: 10.2174/1389557516666160505120157.
3
Chemistry and Biology of the Pyrrole-Imidazole Alkaloids.吡咯 - 咪唑生物碱的化学与生物学
Alkaloids Chem Biol. 2017;77:117-219. doi: 10.1016/bs.alkal.2016.12.001. Epub 2017 Jan 20.
4
Precursor-Guided Mining of Marine Sponge Metabolomes Lends Insight into Biosynthesis of Pyrrole-Imidazole Alkaloids.先驱物导向的海洋海绵代谢组学挖掘为吡咯并咪唑生物碱生物合成提供了新视角。
ACS Chem Biol. 2020 Aug 21;15(8):2185-2194. doi: 10.1021/acschembio.0c00375. Epub 2020 Jul 29.
5
Marine bromopyrrole alkaloids: synthesis and diverse medicinal applications.海洋溴吡咯生物碱:合成及其多样的医学应用。
Curr Top Med Chem. 2014;14(2):253-73. doi: 10.2174/1568026613666131216110001.
6
Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids.吡咯并[2,1- a ]咪唑海洋生物碱的生物合成、不对称合成和药理学,包括细胞靶点。
Nat Prod Rep. 2011 Jul;28(7):1229-60. doi: 10.1039/c0np00013b. Epub 2011 May 9.
7
Marine-Derived Macrocyclic Alkaloids (MDMAs): Chemical and Biological Diversity.海洋来源的大环生物碱(MDMAs):化学和生物多样性。
Mar Drugs. 2020 Jul 17;18(7):368. doi: 10.3390/md18070368.
8
Dimeric pyrrole-imidazole alkaloids: sources, structures, bioactivities and biosynthesis.二聚吡咯并咪唑生物碱:来源、结构、生物活性与生物合成。
Bioorg Chem. 2023 Apr;133:106332. doi: 10.1016/j.bioorg.2022.106332. Epub 2022 Dec 20.
9
Recent Discovery of Nitrogen Heterocycles from Marine-Derived Species.海洋源物种中氮杂环的最新发现。
Mar Drugs. 2024 Jul 18;22(7):321. doi: 10.3390/md22070321.
10
Pyrrole carboxamide introduction in the total synthesis of pyrrole-imidazole alkaloids.吡咯酰胺在吡咯并咪唑生物碱全合成中的应用。
Org Biomol Chem. 2021 Mar 28;19(12):2603-2621. doi: 10.1039/d0ob02052d. Epub 2021 Mar 8.

引用本文的文献

1
Quantum Chemical Studies on the Prototropic and Acid/Base Equilibria for 2-Aminopyrrole in Vacuo-Role of CH Tautomers in the Design of Strong Brønsted Imino N-Bases.真空中2-氨基吡咯的质子转移和酸碱平衡的量子化学研究——CH互变异构体在强布朗斯特亚氨基N-碱设计中的作用
Molecules. 2025 May 9;30(10):2112. doi: 10.3390/molecules30102112.
2
Development and Perfection of Marine-Based Insecticide Biofilm for Pea Seed Protection: Experimental and Computational Approaches.用于豌豆种子保护的海洋基杀虫剂生物膜的开发与完善:实验与计算方法
Molecules. 2025 Apr 4;30(7):1621. doi: 10.3390/molecules30071621.
3
Advances in the Total Synthesis of Pharmacologically Important Fused Indolizidine Alkaloids: Securinine, Gephyrotoxin and Lepadiformine.

本文引用的文献

1
Synthesis of lamellarin R, lukianol A, lamellarin O and their analogues.片螺素R、卢卡诺醇A、片螺素O及其类似物的合成。
RSC Adv. 2020 Nov 27;10(70):43168-43174. doi: 10.1039/d0ra09249e. eCollection 2020 Nov 23.
2
Total synthesis of (+)-spiroindimicin A and congeners unveils their antiparasitic activity.(+)-螺旋吲哚霉素A及其类似物的全合成揭示了它们的抗寄生虫活性。
Chem Sci. 2021 Jun 30;12(30):10388-10394. doi: 10.1039/d1sc02838c. eCollection 2021 Aug 4.
3
Marine Natural Products: A Potential Source of Anti-hepatocellular Carcinoma Drugs.
具有药理学重要性的稠合中氮茚生物碱全合成研究进展:一叶萩碱、盖普托毒素和扁海鞘碱。
Curr Org Synth. 2025;22(3):288-309. doi: 10.2174/0115701794332632240918043021.
4
Unlocking the Potential of Pyrrole: Recent Advances in New Pyrrole-Containing Compounds with Antibacterial Potential.释放吡咯的潜力:具有抗菌潜力的新型含吡咯化合物的最新进展
Int J Mol Sci. 2024 Nov 29;25(23):12873. doi: 10.3390/ijms252312873.
5
Indium(III)-Catalyzed Synthesis of Pyrroles and Benzo[]indoles by Intramolecular Cyclization of Homopropargyl Azides.铟(III)催化高炔丙基叠氮化物分子内环化合成吡咯和苯并吲哚。
J Org Chem. 2024 Nov 1;89(21):16015-16021. doi: 10.1021/acs.joc.4c01768. Epub 2024 Oct 15.
6
An Overview on the Synthesis of Lamellarins and Related Compounds with Biological Interest.层粘连蛋白及其具有生物活性的相关化合物的合成概述。
Molecules. 2024 Aug 26;29(17):4032. doi: 10.3390/molecules29174032.
7
Allostreptopyrroles A-E, β-alkylpyrrole derivatives from an actinomycete sp. RD068384.别链吡咯A - E,一种放线菌属sp. RD068384产生的β - 烷基吡咯衍生物。
Beilstein J Org Chem. 2024 Aug 13;20:1981-1987. doi: 10.3762/bjoc.20.174. eCollection 2024.
8
Marine -Derived Novel Alkaloids Discovered in the Past Decade.过去十年中发现的海洋来源新型生物碱。
Mar Drugs. 2024 Jan 22;22(1):51. doi: 10.3390/md22010051.
9
Pyrrole alkaloids from the fruiting bodies of edible mushroom .来自可食用蘑菇子实体的吡咯生物碱。
RSC Adv. 2023 Jun 16;13(27):18223-18228. doi: 10.1039/d3ra02672h. eCollection 2023 Jun 15.
10
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities.吡咯-2-甲醛:起源与生理活性。
Molecules. 2023 Mar 13;28(6):2599. doi: 10.3390/molecules28062599.
海洋天然产物:抗肝癌药物的潜在来源。
J Med Chem. 2021 Jun 24;64(12):7879-7899. doi: 10.1021/acs.jmedchem.0c02026. Epub 2021 Jun 15.
4
Unequivocal structure confirmation of a breitfussin analog by anisotropic NMR measurements.通过各向异性核磁共振测量对一种布氏菌素类似物进行明确的结构确认。
Chem Sci. 2020 Sep 21;11(44):12081-12088. doi: 10.1039/d0sc03664a.
5
Application of marine natural products in drug research.海洋天然产物在药物研究中的应用。
Bioorg Med Chem. 2021 Apr 1;35:116058. doi: 10.1016/j.bmc.2021.116058. Epub 2021 Feb 9.
6
Design, Synthesis and Structure-Activity Relationship Studies of Glycosylated Derivatives of Marine Natural Product Lamellarin D.糖基化海洋天然产物 Lamellarin D 衍生物的设计、合成及构效关系研究。
Eur J Med Chem. 2021 Mar 15;214:113226. doi: 10.1016/j.ejmech.2021.113226. Epub 2021 Jan 28.
7
Evolution of a Synthetic Strategy for Complex Polypyrrole Alkaloids: Total Syntheses of Curvulamine and Curindolizine.复杂吡咯生物碱合成策略的演变:卷曲霉素和卷曲洛林碱的全合成。
J Am Chem Soc. 2021 Feb 24;143(7):2970-2983. doi: 10.1021/jacs.0c13465. Epub 2021 Feb 11.
8
Complete genome sequence of Streptomyces sp. SCSIO 03032 isolated from Indian Ocean sediment, producing diverse bioactive natural products.从印度洋沉积物中分离得到的产多种生物活性天然产物的链霉菌 SCSIO 03032 的全基因组序列。
Mar Genomics. 2021 Feb;55:100803. doi: 10.1016/j.margen.2020.100803. Epub 2020 Jul 9.
9
Polyphenolic Fraction Obtained From Marine Plant and Thalassiolin B Exert Cytotoxic Effects in Colorectal Cancer Cells and Arrest Tumor Progression in a Xenograft Mouse Model.从海洋植物中获得的多酚组分和海松素B对结肠癌细胞具有细胞毒性作用,并在异种移植小鼠模型中阻止肿瘤进展。
Front Pharmacol. 2020 Nov 30;11:592985. doi: 10.3389/fphar.2020.592985. eCollection 2020.
10
Marine Anticancer Agents: An Overview with a Particular Focus on Their Chemical Classes.海洋抗癌药物:概述及其化学类别特别关注。
Mar Drugs. 2020 Dec 4;18(12):619. doi: 10.3390/md18120619.