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1-Amino-1-desoxy-D-sorbose | 113532-32-4

中文名称
——
中文别名
——
英文名称
1-Amino-1-desoxy-D-sorbose
英文别名
1-amino-1-deoxy-D-sorbitol;1-deoxy-1-aminosorbitol;l-amino-1-deoxysorbitol;1-amino-1-deoxy-sorbitol;(3R,4S,5R)-1-amino-3,4,5,6-tetrahydroxyhexan-2-one
1-Amino-1-desoxy-D-sorbose化学式
CAS
113532-32-4
化学式
C6H13NO5
mdl
——
分子量
179.173
InChiKey
XBBIACPUMILHFE-SRQIZXRXSA-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:
    517.2±50.0 °C(predicted)
  • 密度:
    1.498±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -3.5
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    124
  • 氢给体数:
    5
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • NOVEL QUERCETIN DERIVATIVES AS ANTI-CANCER AGENTS
    申请人:Joshi Narendra Shriram
    公开号:US20110034413A1
    公开(公告)日:2011-02-10
    The present invention provides novel Quercetin derivatives of formula (I) and pharmaceutically acceptable salts, hydrates, and solvates thereof, wherein R 1 is hydrogen, benzyl or substituted benzyl; R 2 is hydrogen, benzyl or substituted benzyl, linear or branched (C 1 -C 6 ) alkyl, substituted alkyl, aryl, substituted aryl, heterocycle and substituted heterocycle, useful for treatment of various disorders including cancer, multi-drug resistant cancers, viral infections etc. The invention also provides a process for the preparation of compounds of formula (I) and pharmaceutical compositions comprising the same.
    本发明提供了新型的槲皮素衍生物及其药用可接受的盐、水合物和溶剂化物, 其中R1为氢、苄基或取代苄基;R2为氢、苄基或取代苄基,直链或支链的(C1-C6)烷基,取代烷基,芳基,取代芳基,杂环和取代杂环,用于治疗包括癌症、多药耐药癌症、病毒感染等多种疾病。本发明还提供了制备公式(I)化合物的方法以及包含该化合物的药物组合物。
  • Radiopharmaceuticals for imaging infection and inflammation
    申请人:——
    公开号:US20030124053A1
    公开(公告)日:2003-07-03
    The present invention provides novel radiopharmaceuticals useful for the diagnosis of infection and inflammation, reagents and kits useful for preparing the radiopharmaceuticals, methods of imaging sites of infection and/or inflammation in a patient, and methods of diagnosing diseases associated with infection or inflammation in patients in need of such diagnosis. The radiopharmaceuticals bind in vivo to the leukotriene B4 (LTB4) receptor on the surface of leukocytes which accumulate at the site of infection and inflammation. The reagents provided by this invention are also useful for the treatment of diseases associated with infection and inflammation.
    本发明提供了用于诊断感染和炎症的新型放射性药物,用于制备这些放射性药物的试剂和工具包,用于在患者体内成像感染和/或炎症部位的方法,以及用于诊断需要此类诊断的患者中与感染或炎症相关的疾病的方法。这些放射性药物在体内与在感染和炎症部位聚集的白细胞表面的白三烯B4(LTB4)受体结合。本发明提供的试剂还可用于治疗与感染和炎症相关的疾病。
  • LTB4 antagonists and radiopharmaceuticals for imaging infection and inflammation
    申请人:Bristol-Myers Squibb Pharma Company
    公开号:EP1293214A3
    公开(公告)日:2003-03-26
    The present invention provides novel radiopharmaceutials useful for the diagnosis of infection and inflammation, reagents and kits useful for preparing the radiopharmaceuticals, methods of imaging sites of infection and/or inflammation in a patient, and methods of diagnosing diseases associated with infection or inflammation in patients in need of such diagnosis. The radiopharmaceuticals bind in vivo to the leukotriene B4 (LTB4) receptor on the surface of leukocytes which accumulate at the site of infection and inflammation. The reagents provided by this invention are also useful for the treatment of diseases associated with infection and inflammation.
    本发明提供了用于诊断感染和炎症的新型放射性药物,用于制备放射性药物的试剂和试剂盒,用于在患者体内成像感染和/或炎症部位的方法,以及用于诊断需要此类诊断的患者中与感染或炎症相关的疾病的方法。这些放射性药物在体内与在感染和炎症部位积聚的白细胞表面的白三烯B4(LTB4)受体结合。本发明提供的试剂还可用于治疗与感染和炎症相关的疾病。
  • ABUSE DETERRENT AND ANTI-DOSE DUMPING PHARMACEUTICAL SALTS USEFUL FOR THE TREATMENT OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER
    申请人:King Clifford Riley
    公开号:US20120028960A1
    公开(公告)日:2012-02-02
    A pharmaceutical composition comprising a drug substance consisting essentially of a pharmaceutically acceptable organic acid addition salt of an amine containing pharmaceutically active compound wherein the amine containing pharmaceutical active compound is selected from the group consisting of racemic or single isomer ritalinic acid or phenethylamine derivatives and the drug substance has a physical form selected from amorphous and polymorphic.
    一种药物组合物,包括基本上由含有药用活性化合物的胺的药用可接受的有机酸加合盐组成的药物物质,其中含有药用活性化合物的胺被选择自光学异构体或单异构体利他林酸或苯乙胺衍生物的群体,并且该药物物质具有从无定形到多型的物理形式。
  • Method of separating isotopes
    申请人:——
    公开号:US20040081604A1
    公开(公告)日:2004-04-29
    A process in which isotopes of the same element belonging to the alkaline earth metals, transition elements and heavy metals having an atomic mass of less than 209, in particular lanthanide metals, are separated in an aqueous medium by treating an aqueous medium.
    一种过程,其中属于碱土金属、过渡金属和重金属同位素,具有小于209的原子质量,特别是镧系金属,在水性介质中通过处理水性介质分离。
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