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methyl (2S,3S,4S,5R)-3,4,5-triformyloxy-6-hydroxyoxane-2-carboxylate

中文名称
——
中文别名
——
英文名称
methyl (2S,3S,4S,5R)-3,4,5-triformyloxy-6-hydroxyoxane-2-carboxylate
英文别名
——
methyl (2S,3S,4S,5R)-3,4,5-triformyloxy-6-hydroxyoxane-2-carboxylate化学式
CAS
——
化学式
C10H12O10
mdl
——
分子量
292.2
InChiKey
ITZRQSCQOQGTAN-NMLRKWPISA-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):
    -0.8
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    135
  • 氢给体数:
    1
  • 氢受体数:
    10

文献信息

  • CHOLINERGIC ENHANCERS WITH IMPROVED BLOOD-BRAIN BARRIER PERMEABILITY FOR THE TREATMENT OF DISEASES ACCOMPANIED BY COGNITIVE IMPAIRMENT
    申请人:Maelicke Alfred
    公开号:US20070213318A1
    公开(公告)日:2007-09-13
    The present invention refers to compounds that, in addition to enhancing the sensitivity to acetylcholine and choline of neuronal cholinergic receptors and/or acting as cholinesterase inhibitors and/or neuroprotective agents, have enhanced blood-brain barrier permeability in comparison to their parent compounds. The compounds are derived (either formally by their chemical structure or directly by chemical synthesis) from natural compounds belonging to the class of amaryllidaceae alkaloids e.g. galanthamine, narwedine and lycoramine, or from metabolites of said compounds. The compounds of the present invention can either interact as such with their target molecules, or they can act as “pro-drugs”, in the sense that after reaching their target regions in the body they are converted by hydrolysis or enzymatic attack to the original parent compound and react as such with their target molecules, or both. The compounds of this invention may be used as medicaments for the treatment of human brain diseases associated with a cholinergic deficit, including the neurodegenerative diseases Alzheimer's and Parkinson's disease and the psychiatric diseases vascular dementia, schizophrenia and epilepsy.
    本发明涉及化合物,除了增强神经元胆碱能受体对乙酰胆碱胆碱的敏感性,或者作为胆碱酯酶抑制剂和/或神经保护剂外,与其母化合物相比,具有增强的血脑屏障渗透性。这些化合物是从天仙子科生物碱类天仙子碱,如无心菜碱、纳尔韦丁和百合碱,或其代谢物中派生的(通过其化学结构或直接通过化学合成)。本发明的化合物可以直接与其目标分子相互作用,也可以作为“前药”,在到达体内目标区域后,通过解或酶攻击转化为原始母化合物,并像母化合物一样与其目标分子反应,或两者兼而有之。本发明的化合物可用作治疗与胆碱能缺陷相关的人类脑疾病的药物,包括神经退行性疾病阿尔茨海默病和帕森病以及精神疾病血管性痴呆、精神分裂症和癫痫。
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