CAS: 471-05-6; (2E,6E,10E)-2,6,9,9-Tetramethylcycloundeca-2,6,10-Trienone

该化合物是一种自然产生的松树素化合物,主要来自Zingiber 贝厂的基本油,通常称为香波姜,其特点是独特的化学结构,包括一个双环框架,Zerumbone以潜在的生物活动而著称,包括抗炎,抗氧化剂和抗癌特性,使其成为药理研究的课题.该化合物一般没有色素,可粉色黄色,有香味.其溶解性特征表明它溶解于有机溶剂,但水溶解性有限.Zerumbone已就其对各种细胞路径及其潜在治疗应用的影响进行了研究,特别是在癌症治疗和预防方面.此外,还评估了其安全特征,在各种研究中显示毒性较低.

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欧盟法规

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合成工艺路线路线简述

    📜Zerumbol置于manganese(Iv) Oxide体系中,用80%的收率获得产物花薑酮
    参考文献:Conversion Of Humulene To Zerumbone
    标题:Conversion Of Humulene To Zerumbone
    摘要:葎草烯首先通过一系列化学反应转化为泽兰酮.
    DOI:10.1246/cl.1981.717

    海关参考信息

    专利信息


    专利号:US-2018105838-A1
    优先权日:2015-03-11
    标 题:Process for de novo microbial synthesis of terpenes
    发明人:SCHRADER JENS; BUCHHAUPT MARKUS; SONNTAG FRANK; KRONER CORA; BRÜSER HEIKE; Schröder Hartwig; PELZER RALF
    权利人:BASF SE
    摘要:The invention relates to microbial terpene production. Known methods for microbial production of terpenes are mostly based on the direct conversion of sugars. Therefore alternative substrates, in particular alternative carbon sources, for use in microbial terpene production were desirable. The invention relates to a methylotrophic bacterium containing recombinant DNA coding for at least one polypeptide with enzymatic activity for heterologous expression in said bacterium, wherein said at least one polypeptide with enzymatic activity is selected from the group consisting an enzyme of a heterologous mevalonate pathway, a heterologous terpene synthase and optionally a heterologous synthase of a prenyl diphosphate precursor. The invention further relates in particular to a method for de novo microbial synthesis of sesquiterpenes or diterpenes from methanol and/or ethanol.

    专利号:US-11612556-B2
    优先权日:2014-12-16
    标 题:Peptidic compounds, compositions comprising them and uses of said compounds, in particular cosmetic uses
    发明人:PESCHARD OLIVIER; DOUCET ANNE; LEROUX RICHARD; MONDON PHILIPPE
    权利人:SEDERMA SA
    摘要:The peptidic compound comprises at least an aminoacid which is lysine, ornithine, diaminopropionic acid or diaminobutyric acid or a derivative of these aminoacids, on which a carboxylic acid is grafted via a peptidic bound on the nitrogen of the lateral chain, said carboxylic acid comprising a (poly)cycle or (poly)heterocycle. Preferably, the grafted carboxylic acid is an aminoacid or a derivative, in particular selected from, a proline, a hydroxyproline or pyroglutamic acid.The peptidic compound can stimulate the synthesis of the main molecules constituting the extracellular matrix of the skin, especially collagen 1 and 4 and elastin. It can be used for topical cosmetic treatment such as a global anti-aging treatment, or for specific activities, including anti-wrinkles, moisturizing, to improve the mechanical properties of the skin, firmness/tone/elasticity/flexibility, to increase density and volume of the skin, improve skin radiance, for a restructuring effect and/or to fight stretch marks.

    专利号:DE-102015103608-A1
    优先权日:2015-03-11
    标题 :Process for the microbial de novo synthesis of terpenes

    专利号:US-10668000-B2
    优先权日:2014-05-22
    标题:Peptides, compositions comprising them and uses in particular cosmetic uses
    发明人:PESCHARD OLIVIER; DOUCET ANNE; LEROUX RICHARD; MONDON PHILIPPE
    权利人:SEDERMA SA
    摘要:The peptides have the general following formula: X-Pro*-Pro*-Xaa-Y in which: •Xaa is selected from Leucine (Leu, L), Arginine (Arg, R), Lysine (Lys, K), Alanine (Ala, A), Serine (Ser, S), and Aspartic acid (Asp, D); •At the N terminal end of the peptide, X is selected from H, —CO—R1 and —SO 2 —R 1 ; •At the C terminal end of the peptide, Y is selected from OH, OR 1 , NH 2 , NHR 1 and NR 1 R 2 ; •R 1 and R 2 are, independently from each other, selected from an alkyle, aryle, aralkyle, alkylaryl, alkoxy and aryloxy group, that can be linear, branched, cyclic, poly-cyclic, non-saturated, hydroxylated, carbonylated, phosphorylated and/or sulfured, and which skeletum can comprise an heteroatom, in particular an O, S and/or N atom; •Pro* correspond to a Proline, an analogue or derivative thereof; •if X is H then Y is selected from OR 1 , NH 2 , NHR 1 and NR 1 R 2 , and if Y is OH then X is —CO— or —SO 2 —R 1 ; and the peptide hypoxanthine-Pro-Pro-Arg being excluded. The invention provides the use of the peptides of above formula I to stimulate the synthesis of the molecules constituting the dermal extracellular matrix, including collagen I and IV and elastin. A cosmetic treatment according to the invention includes anti-aging, anti-wrinkles, improving mechanical properties of the skin, firmness/tone/elasticity/suppleness/flexibility, increasing density and volume of the skin, restructuring effect, fighting stretch marks, improving skin barrier and/or skin hydration.

    专利号:CN-107429223-A
    优先权日:2015-03-11
    标 题 :Methods for de novo microbial synthesis of terpenoids

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