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benzyl 2-deoxy-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranoside | 339316-68-6

中文名称
——
中文别名
——
英文名称
benzyl 2-deoxy-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranoside
英文别名
TrocNH(-2d)Glc(a)-O-Bn;2,2,2-trichloroethyl N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-phenylmethoxyoxan-3-yl]carbamate
benzyl 2-deoxy-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranoside化学式
CAS
339316-68-6
化学式
C16H20Cl3NO7
mdl
——
分子量
444.696
InChiKey
GCFAQXPLDOHSEJ-KSTCHIGDSA-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

物化性质

  • 沸点:
    605.5±55.0 °C(Predicted)
  • 密度:
    1.54±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    27
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    118
  • 氢给体数:
    4
  • 氢受体数:
    7

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

点击查看最新优质反应信息

文献信息

  • [EN] SYNTHETIC INNATE IMMUNE RECEPTOR LIGANDS AND USES THEREOF<br/>[FR] LIGANDS DE RÉCEPTEURS IMMUNITAIRES INNÉS SYNTHÉTIQUES ET UTILISATIONS ASSOCIÉES
    申请人:ALBERTA RES CHEMICALS INC
    公开号:WO2020082162A1
    公开(公告)日:2020-04-30
    An adjuvant formulation includes a monophosphoryl Lipid A (MPLA) analogue, a Pam3CSK4 analogue, or a muramyldipeptide (MDP) analogue, or combinations thereof. The adjuvant may be formulated in soluble form or in a nanoparticle, such as polylactic glycolic acid nanoparticles. A vaccine formulation comprises the adjuvant formulation and an immunogen. Methods of vaccinating an animal include delivering the vaccine formulation to the animal.
    一种辅助剂配方包括一种单磷脂A(MPLA)类似物、一种Pam3CSK4类似物或一种muramyldipeptide(MDP)类似物,或其组合。该辅助剂可以以可溶形式或纳米粒子形式制备,如聚乳酸-聚乙二醇酸纳米粒子。疫苗配方包括该辅助剂配方和一种免疫原。对动物进行疫苗接种的方法包括将疫苗配方输送给动物。
  • SYNTHETIC LIPID-A ANALOGS AND USES THEREOF
    申请人:BIOMIRA, INC.
    公开号:EP1232168A2
    公开(公告)日:2002-08-21
  • [EN] SYNTHETIC LIPID-A ANALOGS AND USES THEREOF<br/>[FR] ANALOGUES DE LIPIDE-A DE SYNTHESE ET LEUR UTILISATION
    申请人:BIOMIRA INC
    公开号:WO2001036433A2
    公开(公告)日:2001-05-25
    New synthetic Lipid-A analogs based on monosaccharide (1) and disaccharide (2) derivatives were designed and prepared in the present invention. Both structures (1) and (2) incorporate novel lipid structures (3) and (4) that are not found in nature. Also, novel disaccharide Lipid-A structures (2) that incorporate novel contingents of uniform lipids and where R1, R4 and R5 are the same substitution group of structure (III) were synthesized. Liposome formulations containing totally synthetic components such as synthetic Lipid-A and synthetic lipopeptide derived from tumor-associated MUC1 mucin are described along with their therapeutic utility. Comparative test results of immunostimulating properties and toxicity of Lipid-A analogs (1) and (2) are included.
  • Enugala, Ramu; Marques, M. Manuel B., ARKIVOC, 2012, vol. 2012, # 6, p. 90 - 100
    作者:Enugala, Ramu、Marques, M. Manuel B.
    DOI:——
    日期:——
  • SYNTHETIC DERIVATIVES OF MPL AND USES THEREOF
    申请人:VARIATION BIOTECHNOLOGIES INC.
    公开号:US20140328876A1
    公开(公告)日:2014-11-06
    In one aspect, the present disclosure provides compounds of formulae (I) and (II). In another aspect, a compound of formula (I) or (II) is formulated into compositions with an antigen, optionally with a vesicle. In some embodiments, compositions are administered intramuscularly.
    在一个方面,本公开提供了式(I)和(II)的化合物。在另一个方面,将式(I)或(II)的化合物与抗原配制成组合物,可选地与囊泡一起。在一些实施方式中,这些组合物是肌肉注射给药的。
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