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4'-deshydroxy-4'-fluoroamodiaquine | 155020-42-1

中文名称
——
中文别名
——
英文名称
4'-deshydroxy-4'-fluoroamodiaquine
英文别名
4'-Dehydroxy-4'-fluoroamodiaquine;7-chloro-N-[3-(diethylaminomethyl)-4-fluorophenyl]quinolin-4-amine
4'-deshydroxy-4'-fluoroamodiaquine化学式
CAS
155020-42-1
化学式
C20H21ClFN3
mdl
——
分子量
357.858
InChiKey
KMLKPUNXHVNTOM-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):
    3.1
  • 重原子数:
    25
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    28.2
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:31a4707cffd18668abb57373f03cc96e
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反应信息

  • 作为产物:
    描述:
    2-fluoro-5-nitrobenzyl 4-methylbenzenesulfonate盐酸三乙胺 、 tin(ll) chloride 作用下, 以 四氢呋喃1,4-二氧六环乙腈 为溶剂, 反应 16.0h, 生成 4'-deshydroxy-4'-fluoroamodiaquine
    参考文献:
    名称:
    [EN] 7-CHLORO-QUINOLIN-4-AMINE COMPOUNDS AND USES THEREOF FOR THE PREVENTION OR TREATMENT OF DISEASES INVOLVING FORMATION OF AMYLOID PLAQUES AND/OR WHERE A DYSFUNCTION OF THE APP METABOLISM OCCURS
    [FR] COMPOSÉS DE 7-CHLORO-QUINOLIN-4-AMINE ET LEURS UTILISATIONS POUR PRÉVENIR OU TRAITER LES MALADIES IMPLIQUANT LA FORMATION DE PLAQUES AMYLOÏDES ET/OU UN DYSFONCTIONNEMENT DU MÉTABOLISME DE L'APP
    摘要:
    本发明涉及具有以下式(I)的化合物,用于预防和/或治疗涉及淀粉样斑块形成和/或APP代谢功能障碍的疾病。
    公开号:
    WO2011073322A1
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文献信息

  • The Effect of Fluorine Substitution on the Metabolism and Antimalarial Activity of Amodiaquine
    作者:Paul M. O'Neill、Anthony C. Harrison、Richard C. Storr、Shaun R. Hawley、Stephen A. Ward、B. Kevin Park
    DOI:10.1021/jm00035a017
    日期:1994.4
    effect of fluorine substitution on the oxidation potential, metabolism, and in vitro antimalarial activity of amodiaquine. The oxidation potentials were measured by cyclic voltammetry, and it was observed that substitution at the 2',6'- and the 4'-positions (2',6'-DIFAQ and 4'-deOH-4'-FAQ) produced analogues with significantly higher oxidation potentials than the parent drug. Fluorine substitution at the
    阿莫地喹(AQ)(2)是一种4-氨基喹啉抗疟药,可引起不良副作用,例如粒细胞缺乏症和肝损害。据信,观察到的药物毒性与亲电子代谢物氨二喹醌亚胺(AQQI)的形成有关,后者可以与细胞大分子结合并引发超敏反应。5'-氟氨二喹(5'-FAQ,3),5',6'-二氟氨二喹(5',6'-DIFAQ,4),2',6'-二氟氨二喹(2',6'-DIFAQ,5) ,2',5',6'-三氟嘧啶(2',5',6'-TRIFAQ,6)和4'-dehydroxy-4'-氟嘧啶(4'-deOH-4'-FAQ,7)合成以评估氟取代对阿莫地喹的氧化潜能,代谢和体外抗疟活性的影响。通过循环伏安法测量氧化电位,观察到在2',6'-和4'-位置的取代(2',6'-DIFAQ和4'-deOH-4'-FAQ)产生了类似物具有比母体药物明显更高的氧化电位。在2',6'-位和4'-位的氟取代也产生了对生物活化更具抗性的类似物。因此2'
  • NEW HETEROCYCLE COMPOUNDS AND USES THEREOF FOR THE PREVENTION OR TREATMENT OF DISEASES INVOLVING FORMATION OF AMYLOID PLAQUES AND/OR WHERE A DYSFUNCTION OF THE APP METABOLISM OCCURS
    申请人:Delacourte Andre
    公开号:US20120283256A1
    公开(公告)日:2012-11-08
    The present invention relates to compounds having the following Formula (I) for use in the prevention and/or the treatment of diseases involving formation of amyloid plaques and/or where a dysfunction of the APP metabolism occurs.
    本发明涉及具有以下式(I)的化合物,用于预防和/或治疗涉及淀粉样斑块形成和/或APP代谢功能紊乱的疾病。
  • Synthesis, Antimalarial Activity, and Preclinical Pharmacology of a Novel Series of 4′-Fluoro and 4′-Chloro Analogues of Amodiaquine. Identification of a Suitable “Back-Up” Compound for <i>N-tert</i>-Butyl Isoquine
    作者:Paul M. O’Neill、Alison E. Shone、Deborah Stanford、Gemma Nixon、Eghbaleh Asadollahy、B. Kevin Park、James L. Maggs、Phil Roberts、Paul A. Stocks、Giancarlo Biagini、Patrick G. Bray、Jill Davies、Neil Berry、Charlotte Hall、Karen Rimmer、Peter A. Winstanley、Stephen Hindley、Ramesh B. Bambal、Charles B. Davis、Martin Bates、Stephanie L. Gresham、Richard A. Brigandi、Federico M. Gomez-de-las-Heras、Domingo V. Gargallo、Silvia Parapini、Livia Vivas、Hollie Lander、Donatella Taramelli、Stephen A. Ward
    DOI:10.1021/jm8012757
    日期:2009.4.9
    On the basis of a mechanistic understanding of the toxicity of the 4-aminoquinoline arnodiaquine (1b), three series of amodiaquine analogues have been prepared where the 4-aminophenol "metabolic alert" has been modified by replacement of the 4'-hydroxy group with a hydrogen, fluorine, or chlorine atom. Following antimalarial assessment and studies on mechanism of action, two candidates were selected for detailed ADME studies and in vitro and in vivo toxicological assessment. 4'-Fluoro-N-tert-butylamodiaquine (2k) was subsequently identified as a candidate for further development studies based on potent activity versus chloroquine-sensitive and resistant parasites,, moderate to excellent oral bioavailability, low toxicity in in vitro studies, and an acceptable safety profile.
  • US8680095B2
    申请人:——
    公开号:US8680095B2
    公开(公告)日:2014-03-25
  • [EN] 7-CHLORO-QUINOLIN-4-AMINE COMPOUNDS AND USES THEREOF FOR THE PREVENTION OR TREATMENT OF DISEASES INVOLVING FORMATION OF AMYLOID PLAQUES AND/OR WHERE A DYSFUNCTION OF THE APP METABOLISM OCCURS<br/>[FR] COMPOSÉS DE 7-CHLORO-QUINOLIN-4-AMINE ET LEURS UTILISATIONS POUR PRÉVENIR OU TRAITER LES MALADIES IMPLIQUANT LA FORMATION DE PLAQUES AMYLOÏDES ET/OU UN DYSFONCTIONNEMENT DU MÉTABOLISME DE L'APP
    申请人:INST NAT SANTE RECH MED
    公开号:WO2011073322A1
    公开(公告)日:2011-06-23
    The present invention relates to compounds having the following Formula (I) for use in the prevention and/or the treatment of diseases involving formation of amyloid plaques and/or where a dysfunction of the APP metabolism occurs.
    本发明涉及具有以下式(I)的化合物,用于预防和/或治疗涉及淀粉样斑块形成和/或APP代谢功能障碍的疾病。
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