9-Oxoundecanoic acid | 91267-42-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 9-Oxoundecanoic acid
• CAS: 91267-42-4
• 化学式: C₁₁H₂₀O₃
• 分子量: 200.27
• InChiKey: KUPZGNQJONLIRP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  14
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• METHOD FOR PRODUCING MEDIUM-CHAIN OMEGA-HYDROXY FATTY ACIDS, ALPHA,OMEGA-DICARBOXYLIC ACIDS, AND OMEGA-AMINO FATTY ACIDS FROM LONG-CHAIN FATTY ACIDS BY BIOTRANSFORMATION
  申请人：EHWA UNIVERSITY - UNIVERSITY COLLABORATION FOUNDATION

  公开号：US20150057461A1

  公开（公告）日：2015-02-26

  The present invention relates to a transformant which is transformed to express Baeyer-Villiger monooxygenase (BVMO), a method for producing C5-C14 medium-chain ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids, or alcohols from C16-C20 long-chain fatty acids by biotransformation using the transformant, a method for producing a fatty acid derivative having an ester group which is introduced into the chain thereof from keto fatty acid using the BVMO, and novel ω-hydroxy fatty acids which are prepared by the method. Degradation products such as C5 to C14 ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids, alcohols can be produced in a large amount from C16 to C20 long-chain fatty acids contained in a medium by biotransformation using a transformant capable of expressing BVMO of the present invention. Therefore, it can be widely used to produce ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids or alcohols in a more safe and economic manner.

  本发明涉及一种转化体，该转化体被转化以表达Baeyer-Villiger单加氧酶（BVMO），以及通过使用该转化体进行生物转化从C16-C20长链脂肪酸中生产C5-C14中链ω-羟基脂肪酸、α，ω-二羧酸、ω-氨基脂肪酸或醇的方法，以及使用BVMO从酮脂肪酸中引入酯基的脂肪酸衍生物的制备方法和新的ω-羟基脂肪酸。通过使用本发明的能够表达BVMO的转化体进行生物转化，可以从介质中含有的C16到C20长链脂肪酸中大量生产C5到C14的ω-羟基脂肪酸、α，ω-二羧酸、ω-氨基脂肪酸、醇等降解产物。因此，它可以广泛用于更安全、更经济地生产ω-羟基脂肪酸、α，ω-二羧酸、ω-氨基脂肪酸或醇。
• METHOD FOR PRODUCING MIDDLE-CHAIN OMEGA-HYDROXY FATTY ACIDS, ALPHA AND OMEGA-DICARBOXYLIC ACIDS, AND OMEGA-AMINO FATTY ACIDS FROM LONG-CHAIN FATTY ACIDS BY BIOTRANSFORMATION
  申请人：Ewha University-Industry Collaboration Foundation

  公开号：EP2835425A1

  公开（公告）日：2015-02-11

  The present invention relates to a transformant which is transformed to express Baeyer-Villiger monooxygenase (BVMO), a method for producing C5-C14 medium-chain ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids, or alcohols from C16-C20 long-chain fatty acids by biotransformation using the transformant, a method for producing a fatty acid derivative having an ester group which is introduced into the chain thereof from keto fatty acid using the BVMO, and novel ω-hydroxy fatty acids which are prepared by the method. Degradation products such as C5 to C14 ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids, alcohols can be produced in a large amount from C16 to C20 long-chain fatty acids contained in a medium by biotransformation using a transformant capable of expressing BVMO of the present invention. Therefore, it can be widely used to produce ω-hydroxy fatty acids, α,ω-dicarboxylic acids, ω-amino fatty acids or alcohols in a more safe and economic manner.

  本发明涉及一种经转化表达拜耳-维利格单加氧酶（BVMO）的转化体，一种利用转化体通过生物转化从C16-C20长链脂肪酸生产C5-C14中链ω-羟基脂肪酸、α，ω-二羧酸、ω-氨基脂肪酸或醇的方法，一种利用转化体从酮脂肪酸生产具有酯基的脂肪酸衍生物的方法、一种利用 BVMO 生产具有酯基的脂肪酸衍生物的方法，该酯基是利用 BVMO 从酮脂肪酸引入其链中的；以及一种利用该方法制备新型ω-羟基脂肪酸的方法。利用能表达本发明 BVMO 的转化体进行生物转化，可从培养基中所含的 C16 至 C20 长链脂肪酸中产生大量降解产物，如 C5 至 C14 ω-羟基脂肪酸、α,ω-二羧酸、ω-氨基脂肪酸、醇类。因此，它可广泛用于以更安全、更经济的方式生产ω-羟基脂肪酸、α,ω-二羧酸、ω-氨基脂肪酸或醇。
• Improved processes for preparing 7-(2-hexyl-5-hydroxy-cyclopentyl)-heptanoic acid
  申请人：IBI- Istituto Biochimico Italiano Giovanni Lorenzini S.p.A.

  公开号：EP0155392B1

  公开（公告）日：1990-05-02
• Use of BVMO (Baeyer-Villiger monooxygenases) and fatty acids
  申请人：Ewha University-Industry Collaboration Foundation

  公开号：EP2835425B1

  公开（公告）日：2018-05-30
• ALCOHOL-MEDIATED ESTERIFICATION OF CARBOXYLIC ACIDS WITH CARBONATES
  申请人：ARCHER DANIELS MIDLAND COMPANY

  公开号：US20160289161A1

  公开（公告）日：2016-10-06

  Esters and a process for making esters from organic acids by means of reacting a carboxylic acid with dialkylcarbonate in an alcohol-containing solvent without any extrinsic acid or base catalyst is described. A benefit of the preparation process is that it can make the separation and extraction of ester products simpler and more facile vis-à-vis conventional isolation techniques.