CAS: 107438-79-9; Ginkgolide J

该化合物是根戈白叶衍生的二叶细胞内酯,以其独特的化学结构和生物活性特性得到承认.作为金果树叶家族的成员,它表现出有选择地对小板活性元素受体有敌意,有助于其在炎症和血管紊乱中的潜在治疗应用.它高纯度和精致的结构使得它对于药理研究,特别是研究...

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    专利号:US-6693091-B2
    优先权日:2002-03-29
    标 题 :Analogs of terpene trilactones from Ginkgo biloba for bioorganic and imaging studies
    发明人:STROMGAARD KRISTIAN; SUEHIRO MAKIKO; NAKANISHI KOJI
    权利人:UNIV COLUMBIA
    摘要:A compound having the structure: n wherein R 1 is H, OH, a photoactivatable moiety, a fluorescent moiety, or a radioactive moiety; n wherein R 2 is H, OH, a photoactivatable moiety, a fluorescent moiety, or a radioactive moiety; n wherein R 3 is H or OH; n wherein R 4 is H, OH, a photoactivatable moiety, a fluorescent moiety, or a radioactive moiety; and n wherein at least one of R 1 , R 2 , R 3 , or R 4 is a photoactivatable moiety, a fluorescent moiety, or a radioactive moiety. Optically pure enantiomers and salts of the compound are also described. Also, the synthesis of the compound, and uses of the compound, such as in a method for detecting the localization of, or identifying, receptors, enzymes or other targets, whether in a cell or in a subject.

    专利号:US-2009221019-A1
    优先权日:2005-06-22
    标 题:Core-Modified Terpene Trilactones From Ginkgo Biloba Extract and Biological Evaluation Thereof
    发明人:NAKANISHI KOJI; DZYUBA SERGEI; ISHII HIDEKI
    权利人:NAKANISHI KOJI; DZYUBA SERGEI; ISHII HIDEKI
    摘要:Lactone-rings of ginkgolides are converted into the corresponding tetrahydrofuran moieties via DIBAL-H reduction followed by deoxygenation of the formed lactols with Et 3 SiH/BF 3 Et 2 O producing a series of lactol-free ginkgolides. The present invention also relates to synthesis of hydroxyl-free, or hydroxyl-free and lactone-free, ginkgolides and bilobalides.

    专利号:CN-108117561-A
    优先权日:2016-11-30
    标 题 :A kind of mesylate amine ginkgolide B metabolite and its synthesis and purification method

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    主要参考文献


    1: Lau AJ, Yang G, Yap CW, Chang TK. Selective agonism of human pregnane X receptor by individual ginkgolides. Drug Metab Dispos. 2012 Jun;40(6):1113-21. doi: 10.1124/dmd.112.045013. Epub 2012 Mar 5. doi: 10.1016/j.lfs.2014.08.006. Epub 2014 Aug 17. Epub 2002 Feb 28. doi: 10.1002/biof.1151. Epub 2013 Nov 20. Epub 2007 Jul 20.
    7: Scholtyssek H, Damerau W, Wessel R, Schimke I. Antioxidative activity of ginkgolides against superoxide in an aprotic environment. Chem Biol Interact. 1997 Oct 24;106(3):183-90. doi: 10.1124/jpet.110.172338. Epub 2010 Aug 25. Epub 2005 Oct 28. Epub 2006 Sep 12. doi: 10.1016/j.jep.2012.11.038. Epub 2012 Dec 5. doi: 10.1002/mrc.3829. Epub 2012 Jun 22.
    15: Avula B, Wang YH, Smillie TJ, Khan IA. Column liquid chromatography/electrospray ionization-time of flight-mass spectrometry and ultraperformance column liquid chromatography/mass spectrometry methods for the determination of ginkgolides and bilobalide in the leaves of Ginkgo biloba and dietary supplements. J AOAC Int. 2009 Mar-Apr;92(2):645-52. doi: 10.1124/jpet.111.186130. Epub 2011 Aug 23. Review.

    合成参考文献


    参考文献:10.5281/zenodo.5794106
    摘要:The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata) | DOI:10.5281/zenodo.5794106
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