CAS: 142628-53-3; 2,4,6-Trihydroxy-5-((R)-3-Methyl-1-((1Ar,4Ar,7S,7Ar,7Br)-1,1,7-Trimethyl-4-Methylenedecahydro-1H-Cyclopropa[e]Azulen-7-yl)Butyl)Isophthalaldehyde

该化合物是一种天然化合物,主要来自马卡兰加基因的叶子和水果,特别是马卡兰加钽铁,主要来自马卡兰加基因的叶子和水果,它呈现出一个复杂的结构,其特点是多芳香环和氢氧基组,有助于其潜在的生物活动.Mcrocarpal C由于报告的抗氧化剂,抗炎和抗微生物特性,在药化学领域引起了兴趣.这些特征表明它在各种治疗应用中的潜在用途,包括开发用于健康补充或药物的天然产品.此外,它独特的化学结构可以进一步探索合成化学,以提高其功效或生物利用率.与许多天然化合物一样,它也在不断进行研究,以充分阐明其行动机制以及健康和疾病管理的潜在利益.

结构式图片

上下游产品

2,4>undec-11-yl)-3'-methylbutyl>-2,4,6-trimethoxyisophthalaldehyde(+)-5-(1'R)-1'-((1R,2R,4R,8R,11S)-3,3,11-trimethyl-7-methylenetricyclo6.3.0.02,4undec-11-yl)-3'-methylbutyl-2,4,6-trimethoxyisophthalaldehyde 2,4>undec-11-yl)-3'-methylbutyl>-2,4,6-trimethoxybenzene-1,3-dimethanol(+)-5-(1'R)-1'-((1R,2R,4R,8R,11S)-3,3,11-trimethyl-7-methylenetricyclo6.3.0.02,4undec-11-yl)-3'-methylbutyl-2,4,6-trimethoxybenzene-1,3-dimethanol (1aR,4S,7R,7aR,7bR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-1,1,7-trimethyl-1a,3,4,7,7a,7b-hexahydro-1H,2H-cyclopropa[e]azulen-6-one -3,3,11-trimethyltricyclo2,4>undeca-8,10-diene(-)-(1S,2R,4R,7S)-10-(tert-butyldimethylsiloxy)-7-(tert-butyldimethylsiloxy)methyl-3,3,11-trimethyltricyclo6.3.0.02,4undeca-8,10-diene 35H52O8C35H52O8 (1aR,4R,4aR,7S,7aS,7bR)-7-[(R)-1-(3,5-Bis-hydroxymethyl-2,4,6-trimethoxy-phenyl)-3-methyl-butyl]-1,1,4,7-tetramethyl-decahydro-cyclopropa[e]azulen-4-ol 2,4>undec-11-yl)-3'-methylbutyl>-2,4,6-trimethoxybenzene-1,3-dimethanol(+)-5-(1'R)-1'-((1R,2R,4R,8R,11S)-3,3,11-trimethyl-7-methylenetricyclo6.3.0.02,4undec-11-yl)-3'-methylbutyl-2,4,6-trimethoxybenzene-1,3-dimethanol

合成工艺路线路线简述

    📜(-)-Dimethyl 5-<(1'R)-1'-((1R,2R,4R,7S,8R,11S)-7-(Hydroxymethyl)-3,3,11-Trimethyltricyclo<6.3.0.02,4>Undec-9-En-11-yl)-3'-Methylbutyl>-2,4,6-Trimethoxyisophthalate置于palladium On Activated Charcoal 六甲基磷酰三胺,2-硝基苯基丝氰酸酯,四丙基高钌酸铵,三丁基膦,氢气,双氧水,二异丁基氢化铝,Lithium P-Toluenethiolate,N-甲基吗啉氧化物体系中,用 甲醇,甲苯,乙腈 用作溶剂,-78.0~50.0 °C,506.62 Kpa 条件下,反应生成大果桉醛c
    参考文献:First Stereoselective Total Synthesis Of Macrocarpal C: Structure Elucidation Of Macrocarpal G
    标题:First Stereoselective Total Synthesis Of Macrocarpal C: Structure Elucidation Of Macrocarpal G
    摘要:首次实现了大果壳素c的立体选择性全合成,该合成通过硅醚二烯醇与新型六取代苯铬三羰基复合物(作为光学活性苄基阳离子等价物)的偶联反应完成,从而阐明了大果壳素c和大果壳素g的身份.
    Doi:10.1039/a705231F

    海关参考信息

    专利信息


    专利号:US-2002165207-A1
    优先权日:2001-05-02
    标题 :Compositions and methods for the treatment of diabetic neuropathy
    发明人:ROSENBLOOM RICHARD
    摘要:Compositions and a method for the treatment of diabetic neuropathy is disclosed. The compositions comprise a mixture of a compound that promotes synthesis of nerve growth factor, an aldose reductase inhibitor and an antioxidant, optionally formulated in a pharmaceutically acceptable carrier. This combination of active agents provides significant, effective relief of the symptoms of diabetic neuropathy, as well as at least partial recovery of lost neurological function in some cases. In addition, the compositions of the present invention, when used in effective amounts to treat diabetic neuropathy, do not exhibit the severe side effects of many prior art compositions proposed for treatment of this ailment. n In a second aspect, a method for the administration of a composition in accordance with the present invention for the treatment of diabetic neuropathy is disclosed. In the method, an effective amount of the composition of the invention is administered on a regular basis over a period of time sufficient to provide the beneficial effects of relief from the symptoms of diabetic neuropathy, as well as at least some recovery of the damaged nerve tissues.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1021/acs.jnatprod.3c00443
    摘要:Daus M, Hayton JB, Holland DC, Voravuthikunchai SP, Carroll AR, Chakthong S. Camaldulensals A-C, the First Meroterpenoids Possessing Two Spatially Separated Formyl Phloroglucinols Conjugated to a Terpene Core from the Leaves of Eucalyptus camaldulensis Dehnh. J Nat Prod. 2023 Aug 25;86(8):1994–2005. doi: 10.1021/acs.jnatprod.3c00443.
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