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3-oxaspiro[5.5]undecane-8,10-dione | 1058731-65-9

中文名称
——
中文别名
——
英文名称
3-oxaspiro[5.5]undecane-8,10-dione
英文别名
——
3-oxaspiro[5.5]undecane-8,10-dione化学式
CAS
1058731-65-9
化学式
C10H14O3
mdl
MFCD25563407
分子量
182.219
InChiKey
OUGJIWKLAIOBCQ-UHFFFAOYSA-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):
    0.1
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] SUBSTITUTED BICYCLIC DIHYDROPYRIMIDINONES AND THEIR USE AS INHIBITORS OF NEUTROPHIL ELASTASE ACTIVITY<br/>[FR] DIHYDROPYRIMIDINONES BICYCLIQUES SUBSTITUÉES ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE L'ACTIVITÉ ÉLASTASE DE NEUTROPHILES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2014135414A1
    公开(公告)日:2014-09-12
    This invention relates to substituted bicyclic dihydropyrimidinones of formula (1) and their use as inhibitors of neutrophil elastase activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of pulmonary, gastrointestinal and genitourinary diseases, inflammatory diseases of the skin and the eye and other autoimmune and allergic disorders, allograft rejection, and oncological diseases.
    这项发明涉及式(1)的取代双环二氢嘧啶酮及其作为中性粒细胞弹性蛋白酶活性抑制剂的用途,含有这些化合物的药物组合物,以及将其用作治疗和/或预防肺部、胃肠道和泌尿系统疾病、皮肤和眼睛的炎症性疾病以及其他自身免疫和过敏性疾病、移植物排斥反应和肿瘤性疾病的药剂的方法。
  • Substituted Bicyclic Dihydropyrimidinones And Their Use As Inhibitors Of Neutrophil Elastase Activity
    申请人:GNAMM Christian
    公开号:US20140249129A1
    公开(公告)日:2014-09-04
    This invention relates to substituted bicyclic dihydropyrimidinones of formula 1 and their use as inhibitors of neutrophil elastase activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of pulmonary, gastrointestinal and genitourinary diseases, inflammatory diseases of the skin and the eye and other autoimmune and allergic disorders, allograft rejection, and oncological diseases.
    这项发明涉及公式1的取代双环二氢嘧啶酮及其作为中性粒细胞弹性蛋白酶活性抑制剂的用途,包含这些化合物的药物组合物,以及将其用作治疗和/或预防肺部、胃肠道和泌尿系统疾病、皮肤和眼睛的炎症性疾病以及其他自身免疫和过敏性疾病、移植物排斥反应和肿瘤性疾病的方法。
  • Furo-3-carboxamide derivatives and methods of use
    申请人:AbbVie Inc.
    公开号:US09777020B2
    公开(公告)日:2017-10-03
    Compounds of formula (I) and pharmaceutically acceptable salts, esters, amides, or radiolabelled forms thereof, wherein R1, Z1, Z2, and n are as defined in the specification, are useful in treating conditions or disorders prevented by or ameliorated by Tropomysin receptor kinases (Trk). Methods for making the compounds are disclosed. Also disclosed are pharmaceutical compositions of compounds of formula (I), and methods for using such compounds and compositions.
    式(I)的化合物及其药学上可接受的盐、酯、酰胺或放射标记形式,在该式中R1、Z1、Z2和n如规范中所定义,可用于治疗由Tropomysin受体激酶(Trk)预防或改善的症状或疾病。公开了制备这些化合物的方法。还公开了式(I)化合物的药物组合物,以及使用这些化合物和组合物的方法。
  • [EN] REMOVAL OF SENESCENCE-ASSOCIATED MACROPHAGES<br/>[FR] ÉLIMINATION DE MACROPHAGES ASSOCIÉS À LA SÉNESCENCE
    申请人:EVERON BIOSCIENCES INC
    公开号:WO2017189553A1
    公开(公告)日:2017-11-02
    In various aspects and embodiments provided are compounds, compositions and methods relating to aging, senescent cells (SCs) and/or senescence associate macrophages (SAMs). In certain aspects and embodiments provided are compounds and compositions that selectively kill or reprogram senescent cells (SCs) and or senescence associate macrophages (SAMs) and associated methods. In some embodiments, the compounds compositions and methods treat or reverse aging and/or age-related diseases.
    在提供的各种方面和实施例中,涉及与衰老、衰老细胞(SCs)和/或衰老相关巨噬细胞(SAMs)有关的化合物、组合物和方法。在某些方面和实施例中,提供了选择性杀死或重新编程衰老细胞(SCs)和/或衰老相关巨噬细胞(SAMs)的化合物和组合物以及相关方法。在一些实施例中,这些化合物、组合物和方法用于治疗或逆转衰老和/或与年龄相关的疾病。
  • [EN] NOVEL HERBICIDES<br/>[FR] NOUVEAUX HERBICIDES
    申请人:SYNGENTA LTD
    公开号:WO2010081755A1
    公开(公告)日:2010-07-22
    Compounds of formula (I), wherein the substituents are as defined in claim 1, are suitable for use as herbicides.
    式(I)的化合物,其中取代基如权利要求1所定义的那样,适用作为除草剂。
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