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(2R,3R,4R,5R,6R)-5-Acetamido-2-(acetoxymethyl)-6-(2-(2-(((benzyloxy)carbonyl)amino)ethoxy)ethoxy)tetrahydro-2H-pyran-3,4-diyl diacetate | 1261568-35-7

中文名称
——
中文别名
——
英文名称
(2R,3R,4R,5R,6R)-5-Acetamido-2-(acetoxymethyl)-6-(2-(2-(((benzyloxy)carbonyl)amino)ethoxy)ethoxy)tetrahydro-2H-pyran-3,4-diyl diacetate
英文别名
[(2R,3R,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-[2-[2-(phenylmethoxycarbonylamino)ethoxy]ethoxy]oxan-2-yl]methyl acetate
(2R,3R,4R,5R,6R)-5-Acetamido-2-(acetoxymethyl)-6-(2-(2-(((benzyloxy)carbonyl)amino)ethoxy)ethoxy)tetrahydro-2H-pyran-3,4-diyl diacetate化学式
CAS
1261568-35-7
化学式
C26H36N2O12
mdl
——
分子量
568.578
InChiKey
AQFKCXLKNLSQJI-NHTNDUFYSA-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:
    723.1±60.0 °C(Predicted)
  • 密度:
    1.28±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    40
  • 可旋转键数:
    18
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    174
  • 氢给体数:
    2
  • 氢受体数:
    12

安全信息

  • 危险性防范说明:
    P501,P270,P264,P280,P302+P352,P337+P313,P305+P351+P338,P362+P364,P332+P313,P301+P312+P330
  • 危险性描述:
    H302,H315,H319

制备方法与用途

2-乙酰氨基-3,4,6-三-O-乙酰基-1-O - [(N-CBZ基氨基乙氧基)乙氧基] -2-脱氧-B-D吡喃半乳糖可用作医药中间体。

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] TREATMENT OF MST1R RELATED DISEASES AND DISORDERS<br/>[FR] TRAITEMENT DE MALADIES ET DE TROUBLES LIÉS À MST1R
    申请人:EMPIRICO INC
    公开号:WO2022266042A1
    公开(公告)日:2022-12-22
    Disclosed herein are compositions comprising an oligonucleotide that targetsMST1R. The oligonucleotide may include a small interfering RNA (siRNA) or an antisense oligonucleotide (ASO). Also provided herein are methods of treating conditions associated withMST1Rmutations that include providing an oligonucleotide that targetsMST1Rto a subject.
    本文公开了一种含有靶向MST1R的寡核苷酸的组合物。该寡核苷酸可能包括小干扰RNA(siRNA)或反义寡核苷酸(ASO)。本文还提供了一种治疗与MST1R突变相关疾病的方法,包括向受试者提供靶向MST1R的寡核苷酸。
  • [EN] TREATMENT OF PLIN1 RELATED DISEASES AND DISORDERS<br/>[FR] TRAITEMENT DE MALADIES ET DE TROUBLES LIÉS À PLIN1
    申请人:EMPIRICO INC
    公开号:WO2022266132A1
    公开(公告)日:2022-12-22
    Disclosed herein are compositions comprising an oligonucleotide that targets PLIN1. The oligonucleotide may include a small interfering RNA (siRNA) or an antisense oligonucleotide (ASO). Also provided herein are methods of treating conditions associated withPLIN1gene mutations that include providing an oligonucleotide that targets PLIN1 in a subject.
    本文披露了一种含有靶向PLIN1的寡核苷酸的组合物。该寡核苷酸可以包括小干扰RNA(siRNA)或反义寡核苷酸(ASO)。本文还提供了一种治疗与PLIN1基因突变相关疾病的方法,该方法包括向受试者提供靶向PLIN1的寡核苷酸。
  • Targeting ligands
    申请人:Arrowhead Pharmaceuticals, Inc.
    公开号:US10294474B2
    公开(公告)日:2019-05-21
    Described are novel targeting ligands that may be linked to compounds, such therapeutic compounds that are useful in directing the compounds to the in vivo target. The targeting ligands disclosed herein can serve to target expression-inhibiting oligomeric compounds, such as RNAi agents, to liver cells to modulate gene expression. The targeting ligands disclosed herein, when conjugated to a therapeutic compound, may be used in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Compositions including the targeting ligands disclosed herein when linked to expression-inhibiting oligomeric compounds are capable of mediating expression of target nucleic acid sequences in liver cells, such as hepatocytes, which may be useful in the treatment of diseases or conditions that respond to inhibition of gene expression or activity in a cell, tissue, or organism.
    本文介绍的新型靶向配体可与化合物(如治疗性化合物)连接,有助于将化合物导向体内靶点。本文公开的靶向配体可用于将表达抑制性寡聚化合物(如 RNAi 制剂)靶向肝细胞,以调节基因表达。本文公开的靶向配体与治疗化合物连接后可用于多种应用,包括治疗、诊断、靶点验证和基因组发现应用。包括本文公开的靶向配体的组合物与表达抑制性低聚化合物连接时,能够介导肝细胞(如肝细胞)中靶核酸序列的表达,这可能有助于治疗对细胞、组织或生物体中基因表达或活性的抑制有反应的疾病或病症。
  • Targeting Ligands
    申请人:Arrowhead Pharmaceuticals, Inc.
    公开号:US20180064819A1
    公开(公告)日:2018-03-08
    Described are novel targeting ligands that may be linked to compounds, such therapeutic compounds that are useful in directing the compounds to the in vivo target. The targeting ligands disclosed herein can serve to target expression-inhibiting oligomeric compounds, such as RNAi agents, to liver cells to modulate gene expression. The targeting ligands disclosed herein, when conjugated to a therapeutic compound, may be used in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Compositions including the targeting ligands disclosed herein when linked to expression-inhibiting oligomeric compounds are capable of mediating expression of target nucleic acid sequences in liver cells, such as hepatocytes, which may be useful in the treatment of diseases or conditions that respond to inhibition of gene expression or activity in a cell, tissue, or organism.
  • [EN] TARGETING LIGANDS<br/>[FR] LIGANDS DE CIBLAGE
    申请人:ARROWHEAD PHARMACEUTICALS INC
    公开号:WO2018044350A1
    公开(公告)日:2018-03-08
    Described are novel targeting ligands that may be linked to compounds, such therapeutic compounds that are useful in directing the compounds to the in vivo target. The targeting ligands disclosed herein can serve to target expression-inhibiting oligomeric compounds, such as RNAi agents, to liver cells to modulate gene expression. The targeting ligands disclosed herein, when conjugated to a therapeutic compound, may be used in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Compositions including the targeting ligands disclosed herein when linked to expression- inhibiting oligomeric compounds are capable of mediating expression of target nucleic acid sequences in liver cells, such as hepatocytes, which may be useful in the treatment of diseases or conditions that respond to inhibition of gene expression or activity in a cell, tissue, or organism.
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