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3-Hydroxy-15-methyl-hexadecanoic acid 2,5-dioxo-pyrrolidin-1-yl ester | 103196-78-7

中文名称
——
中文别名
——
英文名称
3-Hydroxy-15-methyl-hexadecanoic acid 2,5-dioxo-pyrrolidin-1-yl ester
英文别名
——
3-Hydroxy-15-methyl-hexadecanoic acid 2,5-dioxo-pyrrolidin-1-yl ester化学式
CAS
103196-78-7
化学式
C21H37NO5
mdl
——
分子量
383.528
InChiKey
QPEUXTNORUYCEK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.29
  • 重原子数:
    27.0
  • 可旋转键数:
    15.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    83.91
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Structural verification via convergent total synthesis of dipeptide–lipids isolated from Porphyromonas gingivalis
    摘要:
    A periodontal pathogen, Porphyromonas gingivalis, produces two serine dipeptide lipid classes that we labeled lipid 654 and lipid 430, and both contain L-serine as the terminal amino acid. The lipid 654 and lipid 430 classes are each comprised of three species with differing fatty acid substitutions, but the most abundant species demonstrate unit masses of either 654 or 430, respectively. Recently we observed that the lipid 654 can be hydrolyzed by specific lipases to lipid 430. However, a substantial percentage of the naturally occurring lipid 654 cannot be enzymatically hydrolyzed to lipid 430. The observed partial hydrolysis could be due to the presence of a mixture of stereoisomers. Testing this theory requires structural verification of our so-called 654 and 430 by total synthesis. We present herein details of the convergent synthesis of lipids 430 and 654, which confirm the proposed structure of P. gingivalis lipid 654 to be (3R and 3S)-L-serine-2. The bis(fatty acid) (3R)-L-serine-2 was prepared as well as the synthetic precursor, serine dipeptide mono-fatty acid (3R)-L-serine-1, which is the structure of lipid 430. We also synthesized the (3S)-L-serine-2 diastereomer as well as (3S)-L-serine-1. Using these synthetic standards, we confirmed that PLA2-mediated hydrolysis of lipid 654 is enantioselective in that only the (3R)-L-serine-2, but not (3S)-L-serine 2 is enzymatically hydrolyzed. (C) 2016 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2016.10.010
  • 作为产物:
    描述:
    11-溴-1-十一醇 在 sodium tetrahydroborate 、 silica gelmagnesiumN,N'-二环己基碳二亚胺 、 tin(ll) chloride 、 lithium hydroxide 、 N-(2,2,6,6-tetramethyl-1-oxopiperidin-1-ium-4-yl)acetamide tetrafluoroborate 作用下, 以 四氢呋喃甲醇乙醇二氯甲烷 为溶剂, 反应 12.0h, 生成 3-Hydroxy-15-methyl-hexadecanoic acid 2,5-dioxo-pyrrolidin-1-yl ester
    参考文献:
    名称:
    Structural verification via convergent total synthesis of dipeptide–lipids isolated from Porphyromonas gingivalis
    摘要:
    A periodontal pathogen, Porphyromonas gingivalis, produces two serine dipeptide lipid classes that we labeled lipid 654 and lipid 430, and both contain L-serine as the terminal amino acid. The lipid 654 and lipid 430 classes are each comprised of three species with differing fatty acid substitutions, but the most abundant species demonstrate unit masses of either 654 or 430, respectively. Recently we observed that the lipid 654 can be hydrolyzed by specific lipases to lipid 430. However, a substantial percentage of the naturally occurring lipid 654 cannot be enzymatically hydrolyzed to lipid 430. The observed partial hydrolysis could be due to the presence of a mixture of stereoisomers. Testing this theory requires structural verification of our so-called 654 and 430 by total synthesis. We present herein details of the convergent synthesis of lipids 430 and 654, which confirm the proposed structure of P. gingivalis lipid 654 to be (3R and 3S)-L-serine-2. The bis(fatty acid) (3R)-L-serine-2 was prepared as well as the synthetic precursor, serine dipeptide mono-fatty acid (3R)-L-serine-1, which is the structure of lipid 430. We also synthesized the (3S)-L-serine-2 diastereomer as well as (3S)-L-serine-1. Using these synthetic standards, we confirmed that PLA2-mediated hydrolysis of lipid 654 is enantioselective in that only the (3R)-L-serine-2, but not (3S)-L-serine 2 is enzymatically hydrolyzed. (C) 2016 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2016.10.010
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文献信息

  • Structure and synthesis of WB-3559 A, B, C and D, new fibrinolytic agents isolated from Flavobacterium sp.
    作者:Itsuo Uchida、Keizo Yoshida、Yoshio Kawai、Shigehiro Takase、Yoshikuni Itoh、Hirokazu Tanaka、Masanobu Kohsaka、Hiroshi Imanaka
    DOI:10.1248/cpb.33.424
    日期:——
    WB-3559 A, B, C, and D are new fibrinolytic agents isolated from Flavobacterium sp. No. 3559. The structure of these four compounds and the total synthesis of WB-3559 D are described.
    WB-3559 A、B、C 和 D 是从黄杆菌第 3559 号分离出来的新型纤维蛋白溶解剂。本文介绍了这四种化合物的结构以及 WB-3559 D 的全合成过程。
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