Suppr超能文献

异贝壳杉烯及其衍生物的合成与生物活性。

Allobetulin and its derivatives: synthesis and biological activity.

机构信息

Molecular Design and Synthesis, Department of Chemistry, University of Leuven, Celestijnenlaan 200F, 3-3001 Leuven, Belgium.

出版信息

Molecules. 2011 Mar 14;16(3):2443-66. doi: 10.3390/molecules16032443.

Abstract

This review covers the chemistry of allobetulin analogs, including their formation by rearrangement from betulin derivatives, their further derivatisation, their fusion with heterocyclic rings, and any further rearrangements of allobetulin compounds including ring opening, ring contraction and ring expansion reactions. In the last part, the most important biological activities of allobetulin derivatives are listed. One hundred and fifteen references are cited and the relevant literature is covered, starting in 1922 up to the end of 2010.

摘要

本文综述了别他灵芝醇类似物的化学性质,包括其通过别他灵芝烷衍生物重排生成,进一步衍生化,与杂环环系融合,以及包括开环、缩环和扩环反应在内的别他灵芝醇化合物的任何进一步重排。最后一部分列出了别他灵芝醇衍生物的最重要的生物活性。引用了 115 篇参考文献,涵盖了 1922 年至 2010 年底的相关文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d94/6259842/fa6cac4a3869/molecules-16-02443-g021.jpg

相似文献

1
Allobetulin and its derivatives: synthesis and biological activity.
Molecules. 2011 Mar 14;16(3):2443-66. doi: 10.3390/molecules16032443.
2
Simple structural modifications confer cytotoxicity to allobetulin.
Bioorg Med Chem. 2015 Jul 1;23(13):3002-12. doi: 10.1016/j.bmc.2015.05.015. Epub 2015 May 12.
3
[Synthesis and cytotoxicity of allobetulin derivatives].
Bioorg Khim. 2014 Sep-Oct;40(5):608-17. doi: 10.1134/s1068162014050082.
4
Cytotoxic heterocyclic triterpenoids derived from betulin and betulinic acid.
Bioorg Med Chem. 2012 Jun 1;20(11):3666-74. doi: 10.1016/j.bmc.2012.03.066. Epub 2012 Apr 11.
5
Allobetulin derived seco-oleananedicarboxylates act as inhibitors of acetylcholinesterase.
Bioorg Med Chem Lett. 2015 Jul 1;25(13):2654-6. doi: 10.1016/j.bmcl.2015.04.086. Epub 2015 May 5.
8
Synthesis and cytotoxicity of triterpenoids derived from betulin and betulinic acid via click chemistry.
J Asian Nat Prod Res. 2015;17(2):159-69. doi: 10.1080/10286020.2014.979164. Epub 2014 Nov 7.

引用本文的文献

1
Novel C-2 Aromatic Heterocycle-Substituted Triterpenoids Inhibit Hedgehog Signaling in GLI1 Overexpression Cancer Cells.
ACS Omega. 2025 Mar 4;10(10):10617-10632. doi: 10.1021/acsomega.4c11479. eCollection 2025 Mar 18.
3
Transformation of Terpenoids and Steroids Using Actinomycetes of the Genus .
Molecules. 2024 Jul 18;29(14):3378. doi: 10.3390/molecules29143378.
5
Catalytic Sulfation of Betulin with Sulfamic Acid: Experiment and DFT Calculation.
Int J Mol Sci. 2022 Jan 29;23(3):1602. doi: 10.3390/ijms23031602.
7
A review of thermal homogeneous catalytic deoxygenation reactions for valuable products.
Heliyon. 2020 Feb 20;6(2):e03446. doi: 10.1016/j.heliyon.2020.e03446. eCollection 2020 Feb.
8
Synthesis, characterization and antibacterial activity of novel heterocycle, coumacine, and two of its derivatives.
Saudi Pharm J. 2018 Sep;26(6):870-875. doi: 10.1016/j.jsps.2018.03.010. Epub 2018 Mar 27.
9
Betulin inhibits lung carcinoma proliferation through activation of AMPK signaling.
Tumour Biol. 2014 Nov;35(11):11153-8. doi: 10.1007/s13277-014-2426-7. Epub 2014 Aug 8.

本文引用的文献

1
19β,28-Ep-oxy-18α-olean-3β-ol.
Acta Crystallogr Sect E Struct Rep Online. 2009 Aug 8;65(Pt 9):o2088-9. doi: 10.1107/S1600536809030311.
2
[Synthesis of new olean-18(19)-ene derivatives from allobetulin].
Bioorg Khim. 2010 Jul-Aug;36(4):552-5. doi: 10.1134/s1068162010040102.
3
[The synthesis of triterpenic amides based on 2,3-seco-1-cyano-19beta,28-epoxy-18alpha-olean-3-oic acid].
Bioorg Khim. 2010 May-Jun;36(3):410-5. doi: 10.1134/s1068162010030143.
4
Inhibitory effect of the natural product betulin and its derivatives against the intracellular bacterium Chlamydia pneumoniae.
Biochem Pharmacol. 2010 Oct 15;80(8):1141-51. doi: 10.1016/j.bcp.2010.06.051. Epub 2010 Jul 6.
5
Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus.
Bioorg Med Chem Lett. 2010 Jul 15;20(14):4088-90. doi: 10.1016/j.bmcl.2010.05.083. Epub 2010 May 25.
6
[A one-step approach to the synthesis of germanicane triterpenoids from allobetulin].
Bioorg Khim. 2010 Jan-Feb;36(1):142-4. doi: 10.1134/s1068162010010164.
7
Synthesis and biological evaluation of antitumour-active betulin derivatives.
Bioorg Med Chem. 2010 Feb;18(3):1344-55. doi: 10.1016/j.bmc.2009.12.024. Epub 2009 Dec 23.
8
Triterpenoids.
Nat Prod Rep. 2010 Jan;27(1):79-132. doi: 10.1039/b808530g. Epub 2009 Nov 26.
9
[Synthesis of olean-18(19)-ene derivatives from betulin].
Bioorg Khim. 2009 Mar-Apr;35(2):253-9. doi: 10.1134/s1068162009020125.
10
Synthesis, cytotoxicity, and haemolytic activity of chacotrioside lupane-type neosaponins and their germanicane-type rearrangement products.
Bioorg Med Chem Lett. 2009 Apr 15;19(8):2310-4. doi: 10.1016/j.bmcl.2009.02.076. Epub 2009 Feb 23.

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