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12',10-diapocarotene-12',10-dial | 35482-79-2

中文名称
——
中文别名
——
英文名称
12',10-diapocarotene-12',10-dial
英文别名
C12-apocarotene-dialdehyde;(all-E)-2,7-dimethyl-deca-2,4,6,8-tetraenedial;2,7-Dimethyl-deca-2,4,6,8-tetraenedial;(2E,4E,6E,8E)-2,7-dimethyldeca-2,4,6,8-tetraenedial
12',10-diapocarotene-12',10-dial化学式
CAS
35482-79-2
化学式
C12H14O2
mdl
——
分子量
190.242
InChiKey
GFXWLWOPYGKKOJ-SZZOTQSASA-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):
    2.4
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    fucoxanthin 在 zinc(II) permanganate 作用下, 以 丙酮 为溶剂, 生成 12',10-diapocarotene-12',10-dial
    参考文献:
    名称:
    类胡萝卜素和相关化合物。第XX部分。岩藻黄质的结构与反应
    摘要:
    岩藻黄质是一种Allenic类胡萝卜素。化学和光谱研究确定其结构为3'-乙酰氧基-5,6-环氧-3,5'-二羟基-6',7'-二氢-5,6,7,8,5',6'-六氢- β-caroten-8-one(15)。
    DOI:
    10.1039/j39690000429
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文献信息

  • Synthesen in der Carotinoid-Reihe 23. Mitteilung Ein Beitrag zur Chromsäure-Oxydation von Polyenen
    作者:U. Schwieter、W. Arnold、W. E. Oberhänsli、N. Rigassi、W. Vetter
    DOI:10.1002/hlca.19710540808
    日期:1971.12.10
    Chromic acid oxidation of polyenes with terminal β-ionylidene groups has been studied. A number of hitherto unknown and unexpected oxidation products has been isolated. A mechanism for these oxidations is discussed.
    研究了带有末端β-亚硫基的多烯的铬酸氧化。已经分离出许多迄今未知和意外的氧化产物。讨论了这些氧化的机理。
  • The human mitochondrial enzyme BCO2 exhibits catalytic activity toward carotenoids and apocarotenoids
    作者:Linda D. Thomas、Sepalika Bandara、Vipulkumar M. Parmar、Ramkumar Srinivasagan、Nimesh Khadka、Marcin Golczak、Philip D. Kiser、Johannes von Lintig
    DOI:10.1074/jbc.ra120.015515
    日期:2020.11
    The enzyme beta-carotene oxygenase 2 (BCO2) converts carotenoids into more polar metabolites. Studies in mammals, fish, and birds revealed that BCO2 controls carotenoid homeostasis and is involved in the pathway for vitamin A production. However, it is controversial whether BCO2 function is conserved in humans, because of a 4-amino acid long insertion caused by a splice acceptor site polymorphism. We here show that human BCO2 splice variants, BCO2a and BCO2b, are expressed as pre-proteins with mitochondrial targeting sequence (MTS). The MTS of BCO2a directed a green fluorescent reporter protein to the mitochondria when expressed in ARPE-19 cells. Removal of the MTS increased solubility of BCO2a when expressed in Escherichia coli and rendered the recombinant protein enzymatically active. The expression of the enzymatically active recombinant human BCO2a was further improved by codon optimization and its fusion with maltose-binding protein. Introduction of the 4-amino acid insertion into mouse Bco2 did not impede the chimeric enzyme's catalytic proficiency. We further showed that the chimeric BCO2 displayed broad substrate specificity and converted carotenoids into two ionones and a central C14-apocarotendial by oxidative cleavage reactions at C9,C10 and C9',C10'. Thus, our study demonstrates that human BCO2 is a catalytically competent enzyme. Consequently, information on BCO2 becomes broadly applicable in human biology with important implications for the physiology of the eyes and other tissues.
  • Carotenoids and related compounds. Part XX. Structure and reactions of fucoxanthin
    作者:R. Bonnett、A. K. Mallams、A. A. Spark、J. L. Tee、B. C. L. Weedon、A. McCormick
    DOI:10.1039/j39690000429
    日期:——
    Fucoxanthin is an allenic carotenoid. Chemical and spectroscopic studies establish its structure as 3′-acetoxy-5,6-epoxy-3,5′-dihydroxy-6′,7′-didehydro-5,6,7,8,5′,6′-hexahydro-β-caroten-8-one (15).
    岩藻黄质是一种Allenic类胡萝卜素。化学和光谱研究确定其结构为3'-乙酰氧基-5,6-环氧-3,5'-二羟基-6',7'-二氢-5,6,7,8,5',6'-六氢- β-caroten-8-one(15)。
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