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N-(2-(N-benzyloxycarbonylglycyl)amino-2-deoxy-β-D-glucopyranosyl)-N-dodecyldodecanamide | 113484-29-0

中文名称
——
中文别名
——
英文名称
N-(2-(N-benzyloxycarbonylglycyl)amino-2-deoxy-β-D-glucopyranosyl)-N-dodecyldodecanamide
英文别名
N-(2-(N-benzyloxycarbonyl-glycinamido)-2-deoxy-β-D-glucopyranosyl)-N-dodecyl-dodecanoamide;benzyl N-[2-[[(2R,3R,4R,5S,6R)-2-[dodecanoyl(dodecyl)amino]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]amino]-2-oxoethyl]carbamate
N-(2-(N-benzyloxycarbonylglycyl)amino-2-deoxy-β-D-glucopyranosyl)-N-dodecyldodecanamide化学式
CAS
113484-29-0
化学式
C40H69N3O8
mdl
——
分子量
720.003
InChiKey
WYUOXTPYQMHCEU-AWRAXSRSSA-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):
    9.6
  • 重原子数:
    51
  • 可旋转键数:
    29
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    158
  • 氢给体数:
    5
  • 氢受体数:
    8

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

反应信息

  • 作为反应物:
    描述:
    N-(2-(N-benzyloxycarbonylglycyl)amino-2-deoxy-β-D-glucopyranosyl)-N-dodecyldodecanamide 在 palladium on activated charcoal 盐酸氢气 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 3.0h, 以88.9%的产率得到N-(2-deoxy-2-glycylamino-β-D-glucopyranosyl)-N-dodecyldodecanamide
    参考文献:
    名称:
    Syntheses of Peptidoglycolipid Analogs with Distinct Immunomodulating Activities
    摘要:
    Amphiphilic 2-amino-2-deoxy-beta-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with amino acids to give peptido-glycopyranosyl amides, some of which exhibited strong immunostimulatory (BAY Q8939, 8) or immunoadjuvant (BAY R1005, 9) activities.
    DOI:
    10.1080/07328300008544102
  • 作为产物:
    描述:
    参考文献:
    名称:
    Syntheses of Peptidoglycolipid Analogs with Distinct Immunomodulating Activities
    摘要:
    Amphiphilic 2-amino-2-deoxy-beta-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with amino acids to give peptido-glycopyranosyl amides, some of which exhibited strong immunostimulatory (BAY Q8939, 8) or immunoadjuvant (BAY R1005, 9) activities.
    DOI:
    10.1080/07328300008544102
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文献信息

  • ——
    作者:LOCKHOFF O.、 HAYAUCHI YUTAKA、 STADLER P.、 STUNKEL K. G.、 STRAISSLE G.、 PA+
    DOI:——
    日期:——
  • N-(2-Aminoacylamido-2-desoxy-hexosyl)-amide, -carbamate und -harnstoffe, Verfahren zu ihrer Herstellung sowie ihre Verwendung in Arzneimitteln
    申请人:BAYER AG
    公开号:EP0206037B1
    公开(公告)日:1992-01-15
  • US4855283A
    申请人:——
    公开号:US4855283A
    公开(公告)日:1989-08-08
  • Syntheses of Peptidoglycolipid Analogs with Distinct Immunomodulating Activities
    作者:Oswald Lockhoff、Yutaka Hayauchi
    DOI:10.1080/07328300008544102
    日期:2000.1
    Amphiphilic 2-amino-2-deoxy-beta-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with amino acids to give peptido-glycopyranosyl amides, some of which exhibited strong immunostimulatory (BAY Q8939, 8) or immunoadjuvant (BAY R1005, 9) activities.
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