CAS: 6871-21-2; (R)-1-Methoxy-5,6,6A,7-Tetrahydro-4H-Dibenzo[de,G]Quinolin-2-Ol

该化合物是一种自然产生的藻类,主要产自某些植物物种,特别是Fabaceae家族的植物.该化合物的特点是分子结构复杂,包括有助于其生物活动的多种功能组.Asimilobine展示了多种药理特性,包括潜在的抗炎和止痛作用,使其对药化学感兴趣.其溶解性特征通常表明有机溶剂的中等溶性,而其稳定性则可能受到诸如pH和温度等环境因素的影响.该化合物与生物系统的互动是一个持续研究的领域,特别是其行动机制和潜在治疗应用.与许多alkaliobine一样,安全和毒性特征对于了解其在传统医学和现代医学中的用途至关重要.

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    专利号:US-12091696-B2
    优先权日:2022-08-10
    标 题 :O-methyltransferase protein with highly specific catalytic function for multiple bias parent nuclei and encoding gene and use thereof
    发明人:CHEN SHA; YU YUETONG
    权利人:INST CHINESE MATERIA MEDICA CHINA ACADEMY OF CMS
    摘要:The present disclosure provides an O-methyltransferase protein with a highly specific catalytic function for multiple benzylisoquinoline alkaloids (BIAs) parent nuclei and an encoding gene and use thereof. Compared with wild-type O-methyltransferase, the O-methyltransferase protein (SEQ ID NO: 2) shows an enhanced enzymatic activity and a wider substrate scope. The O-methyltransferase protein can catalyze O-methylation of backbones from three BIAs, including monobenzylisoquinolines (norcoclaurine, coclaurine, and N-methylcoclaurine), aporphines (asimilobine and N-methylasimilobine), and protoberberines (scoulerine and tetrahydrocolumbamine). Meanwhile, this O-methyltransferase protein is highly regioselective for each backbone. The O-methyltransferase protein catalyzes methylation of the monobenzylisoquinolines at 6-OH and 7-OH, is only active on 6-OH of the backbone of the aporphines, and mainly catalyzes methylation of the protoberberines at 2-OH. Moreover, the O-methyltransferase protein has a stronger catalytic activity and can be used as a biocatalyst for the semi-synthesis of related compounds.

    专利号:CN-114891840-A
    优先权日:2022-05-23
    标 题 :Application of lotus leaf O-methyltransferase and its encoding gene in the synthesis of benzylisoquinoline alkaloids and phenylpropionic acids

    专利号:CN-114891840-B
    优先权日:2022-05-23
    标题:Lotus leaf O-methyltransferase and application of encoding gene thereof in synthesis of benzyl isoquinoline alkaloid and phenylpropionic acid compounds

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    主要参考文献

    1. Jin CM, Lee JJ, Kim YK, Ryu SY, Lim SC, Hwang BY, Lee CK, Lee MK. Effects of asimilobine on dopamine biosynthesis and l-DOPA-induced cytotoxicity in PC12 cells. J Asian Nat Prod Res. 2008 Jul-Aug;10(7-8):747-55. doi: 10.1080/10286020802030892. 74(1):212-218. doi: 10.1007/s11418-019-01368-7. Epub 2019 Nov 9. 24(23):4419. doi: 10.3390/molecules24234419.

    合成参考文献


    参考文献:10.1021/np50091a005
    摘要:Likhitwitayawuid K, Angerhofer CK, Cordell GA, Pezzuto JM, Ruangrungsi N. Cytotoxic and antimalarial bisbenzylisoquinoline alkaloids from Stephania erecta. J Nat Prod. 1993 Jan;56(1):30–8. doi: 10.1021/np50091a005.
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