Suppr超能文献

通过阿片碱的环扭曲获得结构复杂的化合物库。

Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.

机构信息

Roger Adams Laboratory, Department of Chemistry, University of Illinois at Urbana-Champaign , 600 South Mathews Avenue, Urbana, Illinois 61801, United States.

出版信息

Org Lett. 2016 Oct 7;18(19):4852-4855. doi: 10.1021/acs.orglett.6b02333. Epub 2016 Sep 21.

Abstract

Many compound collections used in high-throughput screening are composed of members whose structural complexity is considerably lower than that of natural products. We previously reported a strategy for the synthesis of complex and diverse small molecules from natural products using ring-distortion reactions, called complexity-to-diversity (CtD), and herein, CtD is applied in the synthesis of 16 diverse scaffolds and 65 total compounds from the alkaloid natural product sinomenine. Chemoinformatic analysis shows that these compounds possess complex ring systems and marked three-dimensionality.

摘要

许多用于高通量筛选的化合物库由其结构复杂性明显低于天然产物的成员组成。我们之前报道了一种使用环扭曲反应(称为复杂性到多样性,CtD)从天然产物中合成复杂多样的小分子的策略,在此,CtD 被应用于从生物碱天然产物青藤碱中合成 16 种不同骨架和 65 种总化合物。化学信息学分析表明,这些化合物具有复杂的环系统和显著的三维结构。

相似文献

1
Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.
Org Lett. 2016 Oct 7;18(19):4852-4855. doi: 10.1021/acs.orglett.6b02333. Epub 2016 Sep 21.
5
Morphinane alkaloids with cell protective effects from Sinomenium acutum.
J Nat Prod. 2005 Jul;68(7):1128-30. doi: 10.1021/np050112+.
6
Morphinane alkaloid dimers from Sinomenium acutum.
J Nat Prod. 2008 Jan;71(1):127-9. doi: 10.1021/np0704654. Epub 2007 Dec 15.
7
Two new morphinane alkaloids from Sinomenium acutum.
J Asian Nat Prod Res. 2011 Jun;13(6):523-8. doi: 10.1080/10286020.2011.574617.
9
Efficient three-step one-pot synthesis of a novel 2,3,5-substituted pyrazine library.
ACS Comb Sci. 2011 Sep 12;13(5):449-52. doi: 10.1021/co200062n. Epub 2011 Jul 1.

引用本文的文献

1
Identification of a Selective Anticancer Agent from a Collection of Complex-And-Diverse Compounds Synthesized from Stevioside.
J Am Chem Soc. 2025 Mar 26;147(12):10647-10661. doi: 10.1021/jacs.5c00919. Epub 2025 Mar 11.
2
Chloroformate-mediated ring cleavage of indole alkaloids leads to re-engineered antiplasmodial agents.
Org Biomol Chem. 2024 Oct 30;22(42):8423-8436. doi: 10.1039/d4ob00853g.
5
Target-Agnostic P-Glycoprotein Assessment Yields Strategies to Evade Efflux, Leading to a BRAF Inhibitor with Intracranial Efficacy.
J Am Chem Soc. 2022 Jul 13;144(27):12367-12380. doi: 10.1021/jacs.2c03944. Epub 2022 Jun 27.
6
Recent Advances in Divergent Synthetic Strategies for Indole-Based Natural Product Libraries.
Molecules. 2022 Mar 27;27(7):2171. doi: 10.3390/molecules27072171.
7
Ring Distortion of Vincamine Leads to the Identification of Re-Engineered Antiplasmodial Agents.
ACS Omega. 2021 Jul 28;6(31):20455-20470. doi: 10.1021/acsomega.1c02480. eCollection 2021 Aug 10.
8
Limonin as a Starting Point for the Construction of Compounds with High Scaffold Diversity.
Angew Chem Int Ed Engl. 2021 Jul 12;60(29):16119-16128. doi: 10.1002/anie.202104228. Epub 2021 Jun 10.
9
Facilitating Compound Entry as a Means to Discover Antibiotics for Gram-Negative Bacteria.
Acc Chem Res. 2021 Mar 16;54(6):1322-1333. doi: 10.1021/acs.accounts.0c00895. Epub 2021 Feb 26.

本文引用的文献

2
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chem Commun (Camb). 2016 Jul 28;52(63):9837-40. doi: 10.1039/c6cc04662b.
3
Natural Products as Sources of New Drugs from 1981 to 2014.
J Nat Prod. 2016 Mar 25;79(3):629-61. doi: 10.1021/acs.jnatprod.5b01055. Epub 2016 Feb 7.
4
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Org Lett. 2015 Nov 6;17(21):5432-5. doi: 10.1021/acs.orglett.5b02797. Epub 2015 Oct 20.
5
Cheminformatic comparison of approved drugs from natural product versus synthetic origins.
Bioorg Med Chem Lett. 2015 Nov 1;25(21):4802-4807. doi: 10.1016/j.bmcl.2015.07.014. Epub 2015 Jul 14.
6
Privileged structures: efficient chemical "navigators" toward unexplored biologically relevant chemical spaces.
J Am Chem Soc. 2014 Oct 22;136(42):14629-38. doi: 10.1021/ja508343a. Epub 2014 Oct 13.
7
Which three-dimensional characteristics make efficient inhibitors of protein-protein interactions?
J Chem Inf Model. 2014 Nov 24;54(11):3067-79. doi: 10.1021/ci500487q. Epub 2014 Oct 17.
8
Small-molecule inhibitors of protein-protein interactions: progressing toward the reality.
Chem Biol. 2014 Sep 18;21(9):1102-14. doi: 10.1016/j.chembiol.2014.09.001.
9
Biology-oriented synthesis: harnessing the power of evolution.
J Am Chem Soc. 2014 Aug 27;136(34):11853-9. doi: 10.1021/ja505861d. Epub 2014 Aug 5.
10
Synthesis of bridged oxafenestranes from pleuromutilin.
Angew Chem Int Ed Engl. 2014 Sep 8;53(37):9880-3. doi: 10.1002/anie.201404765. Epub 2014 Jul 17.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验