methyl 17-oxoheptadecanoate | 150630-53-8

• 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: methyl 17-oxoheptadecanoate
• CAS: 150630-53-8
• 化学式: C₁₈H₃₄O₃
• 分子量: 298.466
• InChiKey: WUWQXIAMWCJUJB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  21
• 可旋转键数：
  17
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1-壬基)三苯基溴化磷 、 methyl 17-oxoheptadecanoate 在 六甲基磷酰三胺 、 lithium hexamethyldisilazane 作用下， 生成 methyl (Z)-hexacos-17-enoate
  参考文献：
  名称：

  Kling, Marcel R.; Easton, Christopher J.; Poulos, Alf, Journal of the Chemical Society. Perkin transactions I, 1993, # 10, p. 1183 - 1190

  摘要：

  DOI：
• 作为产物：
  描述：

  methyl 11-iodoundecanoate 在 二甲基硫 、 臭氧 作用下， 反应 21.0h， 生成 methyl 17-oxoheptadecanoate
  参考文献：
  名称：

  Kling, Marcel R.; Easton, Christopher J.; Poulos, Alf, Journal of the Chemical Society. Perkin transactions I, 1993, # 10, p. 1183 - 1190

  摘要：

  DOI：

文献信息

• Pyrimidine nucleoside derivatives having anti-tumor activity, their preparation and use
  申请人：Sankyo Company Limited

  公开号：EP0536936A1

  公开（公告）日：1993-04-14

  Compounds of formula (I): [in which: R¹, R² and R³ are the same or different and each represents a hydrogen atom, an optionally substituted alkanoyl group or an alkenylcarbonyl group, provided that at least one of R¹, R² and R³ represents an unsubstituted alkanoyl group having from 5 to 24 carbon atoms, said substituted alkanoyl group or said alkenylcarbonyl group; and one of R⁴ and R⁵ represents a hydrogen atom and the other represents a cyano group]; have valuable anti-tumour activity.

  式子（I）的化合物：[其中：R¹、R²和R³相同或不同，每个代表氢原子、可选取代的脂肪酰基团或烯基羰基团，前提是至少有一个R¹、R²和R³代表有5到24个碳原子的未取代脂肪酰基团，或者是所述取代的脂肪酰基团或所述烯基羰基团；R⁴和R⁵中的一个代表氢原子，另一个代表氰基]，具有有价值的抗肿瘤活性。
• METHODS AND MATERIALS FOR BIOSYNTHESIZING MULTIFUNCTIONAL, MULTIVARIATE MOLECULES VIA CARBON CHAIN MODIFICATION
  申请人：INVISTA Textiles (U.K.) Limited

  公开号：EP3488000A1

  公开（公告）日：2019-05-29
• US5691319A
  申请人：——

  公开号：US5691319A

  公开（公告）日：1997-11-25
• [EN] METHODS AND MATERIALS FOR BIOSYNTHESIZING MULTIFUNCTIONAL, MULTIVARIATE MOLECULES VIA CARBON CHAIN MODIFICATION<br/>[FR] PROCÉDÉS ET MATÉRIAUX POUR LA BIOSYNTHÈSE DE MOLÉCULES MULTIFONCTIONNELLES ET MULTIDIMENSIONELLES PAR MODIFICATION DE LA CHAÎNE CARBONÉE
  申请人：INVISTA TEXTILES (U K ) LTD

  公开号：WO2018022633A1

  公开（公告）日：2018-02-01

  This document describes biochemical pathways for producing a difunctional product having an odd number of carbon atoms in vitro or in a recombinant host, or salts or derivatives thereof, by forming two terminal functional groups selected from carboxyl, amine, formyl, and hydroxyl groups in an aliphatic carbon chain backbone having an odd number of carbon atoms synthesized from (i) acetyl-CoA and propanedioyl-CoA via one or more cycles of methyl ester shielded carbon chain elongation or (ii) propanedioyl-[acp] via one or more cycles of methyl ester shielded carbon chain elongation, The biochemical pathways and metabolic engineering and cultivation strategies described herein rely on enzymes or homologs accepting methyl ester shielded aliphatic carbon chain backbones and maintaining the methyl ester shield for at least one further enzymatic step following one or more cycles of methyl ester shielded carbon chain elongation.
• Kling, Marcel R.; Easton, Christopher J.; Poulos, Alf, Journal of the Chemical Society. Perkin transactions I, 1993, # 10, p. 1183 - 1190
  作者：Kling, Marcel R.、Easton, Christopher J.、Poulos, Alf

  DOI：——

  日期：——