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4-hydroxy-3-hydroxymethylquinoline | 83342-32-9

中文名称
——
中文别名
——
英文名称
4-hydroxy-3-hydroxymethylquinoline
英文别名
3-(hydroxymethyl)-1H-quinolin-4-one
4-hydroxy-3-hydroxymethylquinoline化学式
CAS
83342-32-9
化学式
C10H9NO2
mdl
——
分子量
175.187
InChiKey
GNIQDGVXTCMZRH-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):
    1.2
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Quinolone derivatives and their use in a method of controlling an
    摘要:
    描述了以下公式的化合物:##STR1## 其中n为0、1或2,R.sup.1为C.sub.1-4烷基、C.sub.1-4烷氧基、C.sub.1-4烷硫基、C.sub.1-4烷基磺酰基、三氟甲基、卤素或硝基,R.sup.2和R.sup.3分别独立地为氢或C.sub.1-4烷基,以及它们的盐。这些化合物在治疗即时超敏反应疾病方面具有用途,并通过适当的甲酰喹啉与丙二酸、叶立德或膦酸酯的反应制备。
    公开号:
    US04390541A1
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文献信息

  • [EN] 10-SUBSTITUTED COLCHICINOIDS AS POTENT ANTICANCER AGENTS<br/>[FR] COLCHICINOÏDES SUBSTITUÉS EN POSITION 10, UTILISÉS COMME AGENTS ANTICANCÉREUX PUISSANTS
    申请人:COUNCIL SCIENT IND RES
    公开号:WO2016059650A1
    公开(公告)日:2016-04-21
    The present invention relates to the compounds of formula I wherein R is as herein described. The present invention particularly relates to synthesis and antiproliferative activity of 10-substituted colchicinoids. Compounds of the invention can be used for prevention or in the treatment of cancer disease.
    本发明涉及式I的化合物,其中R如本文所述。本发明特别涉及10-取代秋水仙碱衍生物的合成和抗增殖活性。发明的化合物可用于预防或治疗癌症疾病。
  • [EN] 1-PROPANOL AND 1-PROPYLAMINE DERIVATIVES AND THEIR USE AS GLUCOCORTICOID LIGANDS<br/>[FR] DERIVES DE 1-PROPANOL ET 1-PROPYLAMINE ET LEUR UTILISATION EN TANT QUE LIGANDS DE GLUCOCORTICOIDE
    申请人:BOEHRINGER INGELHEIM PHARMA
    公开号:WO2004063163A1
    公开(公告)日:2004-07-29
    Compounds of Formula (I) wherein R1, R2 R3, R4, R5, R6, and X are as defiend herein for Formula (IA) and Formula (IB), or a tautomer, prodrug, solvate, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocoricoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.
    式(I)的化合物,其中R1、R2、R3、R4、R5、R6和X如式(IA)和式(IB)中所定义,或其异构体、前药、溶剂化合物或盐;含有这些化合物的药物组合物,以及使用这些化合物调节糖皮质激素受体功能的方法,以及使用这些化合物治疗由糖皮质激素受体功能介导或以炎症、过敏或增殖过程为特征的疾病状态或病况的方法。
  • 3-Methylthiomethyl-and 3-methylsulfinylmethyl-4-quinolinones useful for
    申请人:The Boots Company Limited
    公开号:US04442109A1
    公开(公告)日:1984-04-10
    Novel quinolones of the general formula ##STR1## wherein n is 0, 1 or 2; R.sub.1 is C.sub.1-4 alkyl; and R.sub.3 is hydrogen, C.sub.1-4 alkyl, methoxy, methylthio, halo or trifluoromethyl. These compounds have antihypertensive activity and may be used for treating hypertension in mammals. The quinolones are administered in novel therapeutic compositions comprising a quinolone of the above general formula together with a pharmaceutically acceptable carrier. Processes for making the novel quinolones are described.
    一种新型喹诺酮化合物,通式为##STR1## 其中n为0、1或2;R.sub.1为C.sub.1-4烷基;R.sub.3为氢、C.sub.1-4烷基、甲氧基、甲硫基、卤素或三氟甲基。这些化合物具有降压活性,可用于治疗哺乳动物的高血压。该喹诺酮与药物可接受的载体一起组成新型治疗组合物进行给药。同时还描述了制备新型喹诺酮的方法。
  • [EN] INTRACELLULAR DELIVERY AND MITOCHONDRIAL TARGETING BY FLUORINATION<br/>[FR] ADMINISTRATION INTRACELLULAIRE ET CIBLAGE MITOCHONDRIAL PAR FLUORATION
    申请人:TEXAS A & M UNIV SYS
    公开号:WO2020198646A1
    公开(公告)日:2020-10-01
    In an embodiment, the present disclosure relates to a targeting platform that includes a targeted delivery system including an agent. In some embodiments, the targeted delivery system is modified by fluorination. In some embodiments, the targeted delivery system is electrically charge neutral. In a further embodiment, the present disclosure relates to a method that includes fluorinating a targeting compound with a fluorinating reagent and loading an agent with the fluorinated targeting compound to thereby form a micelle. In an additional embodiment, the present disclosure relates to a targeting platform that includes a fluorinated polymeric system including an agent. In another embodiment, the present disclosure relates to a method that includes fluorinating a targeting compound with a fluorinating reagent and loading an agent with the fluorinated targeting compound to thereby form a micelle. Additionally, the method can include administering the fluorinated targeting compound to a subject.
    在一种实施例中,本公开涉及一种包括代理的定位平台,其中包括一个定向传递系统。在某些实施例中,定向传递系统通过氟化进行修改。在某些实施例中,定向传递系统具有电荷中性。在另一种实施例中,本公开涉及一种方法,其中包括使用氟化试剂氟化定向化合物,并使用氟化定向化合物装载代理以形成胶束。在另一种实施例中,本公开涉及一种包括含有代理的氟化聚合物系统的定位平台。此外,该方法可以包括将氟化定向化合物用于治疗对象。
  • [EN] PQSR MODULATORS<br/>[FR] MODULATEURS DU PQSR
    申请人:HELMHOLTZ ZENTRUM FÜR INFEKTIONSFORSCHUNG GMBH
    公开号:WO2015149821A1
    公开(公告)日:2015-10-08
    The present invention relates to compounds according to general formula (I); to pharmaceutical compositions comprising one or more of the compound(s); and to the use of the compound(s) as anti-infectives.
    本发明涉及一般式(I)的化合物;含有一种或多种化合物的制药组合物;以及将该化合物用作抗感染剂的用途。
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