CAS: 13476-25-0; (10S,10As,E)-5,9-Dimethyl-3,6,10,10A-Tetrahydro-2H-10,1A-(Epoxymethano)Oxireno[2',3':4,5]Cyclodeca[1,2-B]Furan-12-One
该化合物是自然产生的松树类化合物,主要来自某些植物物种,特别是林德林的植物,其特点是复杂的双环结构,有助于其独特的化学特性.林德龙以其潜在的生物活动而著称,包括抗微生物和抗炎影响,使其对药理学研究感兴趣.该化合物通常在基本油类中发现,有独特的芳香,其来源可能不同.其溶解性特征受其缺水性的影响,往往使其在有机溶剂中比在水中更容易溶解.此外,林德龙的稳定性可能受到光和温度等环境因素的影响,这些因素可能导致降解或转化成其他化合物.总的来说,林德兰是天然产品化学中一个令人着迷的研究领域,对医药化学和自然香化合物的发展都有影响.
- 英文名称(10S,10As,E)-5,9-Dimethyl-3,6,10,10A-Tetrahydro-2H-10,1A-(Epoxymethano)Oxireno[2',3':4,5]Cyclodeca[1,2-B]Furan-12-One
- 中文名称乌药醚内酯
- IUPAC名称(10S,10aS,E)-5,9-dimethyl-3,6,10,10a-tetrahydro-2H-10,1a-(epoxymethano)oxireno[2',3':4,5]cyclodeca[1,2-b]furan-12-one
- 其它别名Linderane; 2H-10,1A-(Epoxymethano)Oxireno[4,5]Cyclodeca[1,2-B]Furan-12-One,3,6,10,10A-Tetrahydro-5,9-Dimethyl-, (1As,4E,10S,10As)-; (1As,4E,10S,10As)-3,6,10,10A-Tetrahydro-5,9-Dimethyl-10,1A-(Epoxymethano)-2H-Oxireno[4,5]Cyclodeca[1,2-B]Furan-12-One; (1As,4E,10S,10As)-3,6,10,10A-Tetrahydro-5,9-Dimethyl-2H-10,1A-(Epoxymethano)Oxireno[4,5]Cyclodeca[1,2-B]Furan-12-One; Linderane(Rg); Linderane ,; Linderane, , From Lindera Aggregata (Sims) Kosterm.; Wuyaomineizhi
- CAS编号13476-25-0
- MFCD编号:MFCD07781424
- 分子式:C15H16O4分子量:260.29
- 产品CID: 531136
- 产品分类生物化工 → 植物提取物
物理性质
MSDS等安全信息
- 警示词warning
- 危险描述H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- 防范说明P264Thoroughly clean after treatmentP280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective maskP305If it enters the eyesP351Rinse carefully with water for a few minutesP338Remove the contact lens(If any)And easy to operate,Continue flushingP337If eye irritation persistsP313Obtain medical advice/care
- 危险品标志Xi
- 安全声明24/25
合成工艺路线路线简述
海关参考信息
- 2901210000-乙烯
2901220000-丙烯
2905122000-异丙醇
2905143000-叔丁醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-113684221-B
优先权日:2021-09-10
标 题:Application of benzyl isoquinoline alkaloid and derivative thereof in synthesis of gene Ac6OMT
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-116478941-A
优先权日:2023-02-27
标 题:Application of CYP80G protein and its coding gene in catalyzing the synthesis of aporphine alkaloids in lotus leaf
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
专利号:CN-114874139-B
优先权日:2022-05-27
标 题:Synthesis method of 1-benzyl or allyl 3, 4-dihydroisoquinoline
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
主要参考文献
1: Wang H, Wang K, Mao X, Zhang Q, Yao T, Peng Y, Zheng J. Mechanism-based inactivation of CYP2C9 by linderane. Xenobiotica. 2015;45(12):1037-46. doi: 10.3109/00498254.2015.1041002. Epub 2015 Jun 11. doi: 10.1016/j.fitote.2016.03.020. Epub 2016 Apr 2. Chinese. doi: 10.1021/np900354q. Chinese. doi: 10.3389/fphar.2018.00476. eCollection 2018.
7: Wu Y, Zheng Y, Liu X, Han Z, Ren Y, Gan L, Zhou C, Luan L. Separation and quantitative determination of sesquiterpene lactones in Lindera aggregata (wu-yao) by ultra-performance LC-MS/MS. J Sep Sci. 2010 Apr;33(8):1072-8. doi: 10.1002/jssc.200900768. doi: 10.1016/j.jep.2016.12.025. Epub 2016 Dec 15. pii: E1792. doi: 10.3390/molecules23071792.
合成参考文献
参考文献:10.1002/jccs.199500073
摘要:Wu S, Li W. Chemical Constituents from the Roots of Neolitsea hiiranensis. J Chinese Chemical Soc. 1995 Jun;42(3):555–60. doi: 10.1002/jccs.199500073.
参考文献:10.1021/np9602269
摘要:Chen K, Chang F, Jong T, Wu Y. Two Novel Sesquiterpenes from Neolitsea parvigemma. J. Nat. Prod. 1996 Jan 01;59(7):704–6. doi: 10.1021/np9602269.
参考文献:10.1016/0031-9422(93)85167-p
摘要:Wen-Shyong L, Chang-Yih D. Sesquiterpene lactones from Neolitsea villosa. Phytochemistry. 1993;32(6):1503–7. doi: 10.1016/0031-9422(93)85167-p.
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