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2,10,14-desacetyl taxuyunnanine C | 176590-75-3

中文名称
——
中文别名
——
英文名称
2,10,14-desacetyl taxuyunnanine C
英文别名
[(1S,2S,3S,5S,8S,10S,14S)-2,10,14-trihydroxy-8,12,15,15-tetramethyl-4-methylidene-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] acetate
2,10,14-desacetyl taxuyunnanine C化学式
CAS
176590-75-3
化学式
C22H34O5
mdl
——
分子量
378.509
InChiKey
ADIAYVKSTVCWEQ-YIJNTCITSA-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):
    1.4
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    87
  • 氢给体数:
    3
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    乙酸酐2,10,14-desacetyl taxuyunnanine C吡啶 作用下, 反应 24.0h, 生成 taxuyunnanin C
    参考文献:
    名称:
    来自云南红豆杉细胞培养物的 C-14 氧化紫杉烷
    摘要:
    摘要 从云南红豆杉细胞培养物中分离得到3种C-14氧化紫杉烷。
    DOI:
    10.1016/0031-9422(95)00840-3
  • 作为产物:
    描述:
    taxuyunnanin Csodium hydroxide 作用下, 以 甲醇 为溶剂, 生成 2,10,14-desacetyl taxuyunnanine C10β-hydroxy-2α,5α14β-triacetoxytaxa-4(20),11(12)-diene 、 2,5,10,14-desacetyl taxuyunnanine C 、 (3S,4aS,5S,6S,7S,11S,12aS)-1,2,3,4,4a,5,6,7,8,11,12,12a-dodecahydro-9,12a,13,13-tetramethyl-4-methylene-6,10-methanobenzocyclodecene-3,5,7,11-tetrol 5-acetate 、 10β,14β-dihydroxy-2α,5α-diacetoxy-4(20),11-taxadiene 、 2,14-desacetyl taxuyunnanine C 、 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    Special publicationfn1fn1Papers with this heading have received accelerated publication, due to their particular significance in the field of phytochemistry. Purification and characterization of acetyl coenzyme a: 10-hydroxytaxane O-acetyltransferase from cell suspension cultures of Taxus chinensis
    摘要:
    An O-acetyltransferase that catalyzes the regiospecific acetylation of a range of taxanes possessing an unsubstituted 10-hydroxyl group was detected and purified to apparent electrophoretic homogeneity from a cytosolic fraction of Taxus chinensis cell cultures. The purification involved negative calcium phosphate adsorption, sephadex desalting, DEAE, AcA44 chromatography, HighQ, CHT II, HiTrap Blue, Phenylsepharose and Mimetic Green purification steps. The purified acetyltransferase was found to be a monomeric protein of 71 +/- 1.5 kDa that is highly regio- and stereospecific towards the 10 beta-hydroxyl group of the taxane molecule and is also active towards 10-desacetylbaccatine III. The acetyltransferase reaction had a pH optimum of 9.0 with halfmaximal activities at pH 6.8 and 10.8, respectively. The temperature optimum was at 35 degrees C and the isoelectric point at 5.6. The apparent K-m values for 10-desacetyltaxuyunnanine C and acetyl CoA were 23 and 61 mu M, respectively. The turnover rate for the enzyme using both substrates was 0.2 mol mol(-1) of enzyme. The kinetic optimum was determined to be K-cat/K-m = 8.7 s(-1) L M-1. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0031-9422(98)00674-8
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文献信息

  • C-14 oxygenated taxanes from Taxus yunnanensis cell cultures
    作者:Kedi Cheng、Weishuo Fang、Yujun Yang、Hong Xu、Chao Meng、Man Kong、Wenyi He、Qicheng Fang
    DOI:10.1016/0031-9422(95)00840-3
    日期:1996.5
    Abstract Three C-14 oxygenated taxanes were isolated from Taxus yunnanensis cell cultures.
    摘要 从云南红豆杉细胞培养物中分离得到3种C-14氧化紫杉烷。
  • Special publicationfn1fn1Papers with this heading have received accelerated publication, due to their particular significance in the field of phytochemistry. Purification and characterization of acetyl coenzyme a: 10-hydroxytaxane O-acetyltransferase from cell suspension cultures of Taxus chinensis
    作者:Birgitta Menhard、Meinhart H Zenk
    DOI:10.1016/s0031-9422(98)00674-8
    日期:1999.3
    An O-acetyltransferase that catalyzes the regiospecific acetylation of a range of taxanes possessing an unsubstituted 10-hydroxyl group was detected and purified to apparent electrophoretic homogeneity from a cytosolic fraction of Taxus chinensis cell cultures. The purification involved negative calcium phosphate adsorption, sephadex desalting, DEAE, AcA44 chromatography, HighQ, CHT II, HiTrap Blue, Phenylsepharose and Mimetic Green purification steps. The purified acetyltransferase was found to be a monomeric protein of 71 +/- 1.5 kDa that is highly regio- and stereospecific towards the 10 beta-hydroxyl group of the taxane molecule and is also active towards 10-desacetylbaccatine III. The acetyltransferase reaction had a pH optimum of 9.0 with halfmaximal activities at pH 6.8 and 10.8, respectively. The temperature optimum was at 35 degrees C and the isoelectric point at 5.6. The apparent K-m values for 10-desacetyltaxuyunnanine C and acetyl CoA were 23 and 61 mu M, respectively. The turnover rate for the enzyme using both substrates was 0.2 mol mol(-1) of enzyme. The kinetic optimum was determined to be K-cat/K-m = 8.7 s(-1) L M-1. (C) 1999 Elsevier Science Ltd. All rights reserved.
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