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ethyl 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-1-thio-β-D-xylopyranoside | 1334770-26-1

中文名称
——
中文别名
——
英文名称
ethyl 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-1-thio-β-D-xylopyranoside
英文别名
Ara2Ac3Ac4Ac(a1-4)Xyl2Ac3Ac(b)-SEt;[(3S,4S,5R,6S)-4,5-diacetyloxy-6-[(3R,4S,5R,6S)-4,5-diacetyloxy-6-ethylsulfanyloxan-3-yl]oxyoxan-3-yl] acetate
ethyl 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-1-thio-β-D-xylopyranoside化学式
CAS
1334770-26-1
化学式
C22H32O13S
mdl
——
分子量
536.554
InChiKey
FZCTYVFLYHHQPX-QJDFYSGISA-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):
    0.5
  • 重原子数:
    36
  • 可旋转键数:
    14
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    185
  • 氢给体数:
    0
  • 氢受体数:
    14

反应信息

  • 作为反应物:
    描述:
    ethyl 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-1-thio-β-D-xylopyranoside3β-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)oxy-2α-methoxymethyloxy-olean-12-en-28-oic acid benzyl esterN-碘代丁二酰亚胺三氟甲磺酸三甲基硅酯 作用下, 以 二氯甲烷 为溶剂, 反应 0.67h, 以79%的产率得到3β-[2,3,4-tri-O-acetyl-α-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-β-D-xylopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-glucopyranosyl]oxy-2α-methoxymethyloxy-olean-12-en-28-oic acid benzyl ester
    参考文献:
    名称:
    Synthesis of stryphnoside A, a triterpene saponin isolated from the pericarps of Stryphnodendron fissuratum
    摘要:
    Stryphnoside A, alpha-L-rhamnopyranosyl 3 beta-O-[alpha-L-arabinopyranosyl-(1 -> 4)-beta-D-xylopyranosyl-(1 -> 2)-beta-D-glucopyranosyl]-2 alpha-hydroxyolean-12-en-28-oate, has been synthesized in 11 steps in 15% overall yield starting from the naturally abundant oleanolic acid. Condensation of a partially protected glucopyranosyl donor and 2 alpha, 3 beta-dihydroxyolean-12-en-28-oic acid derivative using inverse glycosylation procedure has significantly simplified the target saponin synthesis. Stryphnoside A exhibited weak cytotoxic activities against tumor cells HeLa, A549, and HepG2 with IC50 at mM level. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.06.006
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of stryphnoside A, a triterpene saponin isolated from the pericarps of Stryphnodendron fissuratum
    摘要:
    Stryphnoside A, alpha-L-rhamnopyranosyl 3 beta-O-[alpha-L-arabinopyranosyl-(1 -> 4)-beta-D-xylopyranosyl-(1 -> 2)-beta-D-glucopyranosyl]-2 alpha-hydroxyolean-12-en-28-oate, has been synthesized in 11 steps in 15% overall yield starting from the naturally abundant oleanolic acid. Condensation of a partially protected glucopyranosyl donor and 2 alpha, 3 beta-dihydroxyolean-12-en-28-oic acid derivative using inverse glycosylation procedure has significantly simplified the target saponin synthesis. Stryphnoside A exhibited weak cytotoxic activities against tumor cells HeLa, A549, and HepG2 with IC50 at mM level. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.06.006
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