CAS: 469-39-6; (2Ar,3R,5As,5Bs,7As,8S,9S,11Ar,12As)-2A,5A,8-Trimethyl-3-((R)-6-Methyl-5-Methyleneheptan-2-yl)Tetradecahydro-1H,12H-Cyclopenta[a]Cyclopropa[e]Phenanthren-9-Ol

该化合物是一种三联苯酚化合物,被归类为酯醇,具体而言,是各种酯类和类固醇生物合成的一种前体,其特点是复杂的多环结构,包括环球环球环环环,与环氧环状环结合,有助于其独特的化学特性.Cyclooucalenol通常在各种植物来源中找到,以其在导致胆固醇和其他酯类的生物合成途径中的作用而著称.该化合物一般不色,不为苍白黄,在水中不溶,但在有机溶剂中可溶.其分子配方反映了碳,氢和氧原子的具体安排,影响其与其他生物分子的再活动与互动.Cyclooucalenol因其潜在的生物活动,包括反氟化和抗硫素特性,在研究中获得了兴趣,尽管需要进一步研究,以充分阐明其药理学潜力.

结构式图片

上下游产品

cycloeucalenone 24-methylenecycloartanol Methanesulfonic acid (R)-2-isopropyl-5-[(3S,4S,9S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexyl ester cyclohomonervilolphthalic acid mono-(24-methylene-9β,19-cyclo-31-nor-lanostan-3β-yl ester) 3β-benzoyloxy-24-methylene-9β,19-cyclo-31-nor-lanostane 24-methylenecycloartanol cycloartanol

合成工艺路线路线简述

    📜Cycloeucalenone置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃 作为反应溶剂,化学反应 3.0H,以7 Mg的收率获得产物3-Epicycloeucalenol
    参考文献:Cycloartane Triterpenes From The Fruit Peel Of Musa Sapientum
    标题:Cycloartane Triterpenes From The Fruit Peel Of Musa Sapientum
    摘要:
    DOI:10.1016/s0031-9422(98)80081-2

    海关参考信息

    专利信息


    专利号:US-7906710-B2
    优先权日:2001-01-05
    标 题:Transgenic plants containing altered levels of steroid compounds
    发明人:KARUNANANDAA BALASULOJINI; POST-BEITTENMILLER MARTHA; VENKATRAMESH MYLAVARAPU; KISHORE GANESH M; THORNE GREGORY M; LEDEAUX JOHN R
    权利人:MONSANTO CO
    摘要:Disclosed are constructs comprising sequences encoding 3-hydroxy-3methylglutaryl-Coenzyme A reductase and at least one other sterol synthesis pathway enzyme. Also disclosed are methods for using such constructs to alter sterol production and content in cells, plants, seeds and storage organs of plants. Also provided are oils and compositions containing altered sterol levels produced by use of the disclosed constructs. Novel nucleotide sequences useful in the alteration of sterol production are also provided. Also provided are cells, plants, seeds and storage organs of plants comprising sequences encoding 3-hydroxy-3methylglutaryl-Coenzyme A reductase, at least one other sterol synthesis pathway enzyme and at least one tocopherol synthesis enzyme.

    专利号:US-3686235-A
    优先权日:1969-10-14
    标 题:Class of liquid crystals
    发明人:NICHOLAS HAROLD J; KNAPP FURN F JR
    权利人:HAROLD J NICHOLAS; FURN F KNAPP JR
    摘要:THE CHEMICAL SYNTHESIS AND ISOLATION FROM NATURAL SOURCES OF A NEW CLASS OF CHOLESTERIC AND SMECTIC LIQUID CRYSTALS ARE DESCRIBED. THESE CONSIST OF VARIOUS FATTY ACID ESTERS OF TETRACYLIC TRIERTENES INCLUDING MEMBERS OF THE CLASS OF 9,19-CYCLOPROPANE TRITERPENES. THESE TRITERPENES INCLUDE 9,19-CYCLOLANOST-24-EN-3B-OL(CYCLOARTENOL), 4A,14A,24B-TRIMETHYL-9,19-CYCLOCHOLESTAN-3B-OL, 24E-METHYL-9,19-CYCLOLANOSTAN-3B-OL(24E-METHYL CYCLOARTANOL) AND 24-DIHYDRO LANOSTEROL AND ALL CHEMICALLY RELATED PRODUCTS.

    专利号:US-2003157583-A1
    优先权日:2001-12-17
    标 题:Methods for determining squalene synthase activity
    发明人:STEVENS DONNA; WANG XIAO-ZHUO; RICE JOHN; NYE BETH; BROADWELL DAVID; GLASSBROOK NORMAN; SEVALA VEERESH; CRAWFORD JOHN; STEWART SANDY
    摘要:The cloning of a truncated Arabidopsis gene expressing squalene synthase, as well as the expression and purification of the squalene synthase, are described. Also described herein is a fluorescent assay using squalene synthase that is amenable to high-throughout use, particularly for studying the regulation of isoprenoid synthesis and identifying squalene synthase inhibitors and promoters. As the formation of squalene is stoichiometric with the depletion of NADPH, the activity of squalene synthase can be evaluated by following the NADPH concentration over time. Squalene synthase activity is determined by combining FPP, NADPH, squalene synthase and a magnesium ion cofactor to form a reaction mixture under conditions suitable for squalene formation, optionally in the presence of a compound being analyzed for its ability to inhibit or promote squalene synthase. The concentration of NADPH over time is determined by subjecting the reaction mixture to UV light and detecting fluorescent light emission.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 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:10.1055/s-2005-871291
    摘要:Gomes AY, de Fátima Souza M, Cortes SF, Lemos VS. Mechanism involved in the spasmolytic effect of a mixture of two triterpenes, cycloartenol and cycloeucalenol, isolated from Herissanthia tiubae in the guinea-pig ileum. Planta Med. 2005 Nov;71(11):1025–9. doi: 10.1055/s-2005-871291.
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