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2-(2-(4-fluorophenyl)thiazol-4-yl)-N-hydroxy-2-methylpropanamide

中文名称
——
中文别名
——
英文名称
2-(2-(4-fluorophenyl)thiazol-4-yl)-N-hydroxy-2-methylpropanamide
英文别名
2-[2-(4-fluorophenyl)-1,3-thiazol-4-yl]-N-hydroxy-2-methylpropanamide
2-(2-(4-fluorophenyl)thiazol-4-yl)-N-hydroxy-2-methylpropanamide化学式
CAS
——
化学式
C13H13FN2O2S
mdl
——
分子量
280.323
InChiKey
UWRCUZFXGDORPD-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):
    2.4
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    90.5
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    [EN] METHODS FOR TREATING NEUROLOGICAL SYMPTOMS ASSOCIATED WITH LYSOSOMAL STORAGE DISEASES
    [FR] MÉTHODES DE TRAITEMENT DE SYMPTÔMES NEUROLOGIQUES ASSOCIÉS À DES MALADIES LYSOSOMALES
    摘要:
    提供了用于治疗或预防与溶酶体贮积病等相关的神经症状和疾病的方法。这些方法包括增强受试者大脑内的神经连接、增加大脑组织体积,或者预防或延迟受试者大脑组织体积的丧失。还提供了用于监测神经疾病的进展或退化,或评估与溶酶体贮积病相关的神经疾病的发作的方法,其中测量了受试者的大脑组织体积。
    公开号:
    WO2021156769A1
  • 作为产物:
    描述:
    2-(2-(4-fluorophenyl)thiazol-4-yl)-2-methylpropanoic acid 以75.4的产率得到2-(2-(4-fluorophenyl)thiazol-4-yl)-N-hydroxy-2-methylpropanamide
    参考文献:
    名称:
    Glucosylceramide synthase inhibitors
    摘要:
    本发明涉及一种对糖基鞘氨醇合酶(GCS)起抑制作用的抑制剂,可用于治疗代谢性疾病,如溶酶体贮积病,单独使用或与酶替代治疗结合使用,以及用于治疗癌症。
    公开号:
    US09139580B2
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文献信息

  • [EN] METHODS FOR TREATING PROTEINOPATHIES<br/>[FR] PROCÉDÉS DE TRAITEMENT DE PROTÉINOPATHIES
    申请人:GENZYME CORP
    公开号:WO2016145046A1
    公开(公告)日:2016-09-15
    This disclosure relates to a method of treating a proteinopathy in a subject, the method comprising administering to the subject an effective amount of a quinuclidine compound. The disclosure also relates to a method of reducing, reversing or preventing the accumulation of protein aggregates in tissue of a subject diagnosed as having a proteinopathy, or being at risk of developing a proteinopathy, the method comprising administering to the subject an effective amount of a quinuclidine compound. Also disclosed is a pharmaceutical composition comprising a quinuclidine compound for use in said methods. The proteinopathy may be a synucleinopathy or a tauopathy, such as Parkinson's disease, Alzheimer's disease or dementia with Lewy bodies.
    这份披露涉及一种治疗受试者蛋白病的方法,该方法包括向受试者施用有效量的环丙胺化合物。该披露还涉及一种减少、逆转或预防被诊断为患有蛋白病或有患蛋白病风险的受试者组织中蛋白聚集物积累的方法,该方法包括向受试者施用有效量的环丙胺化合物。还披露了一种包含环丙胺化合物的药物组合物,用于上述方法。蛋白病可能是突触核蛋白病或tau蛋白病,如帕森病、阿尔茨海默病或带有Lewy小体的痴呆症。
  • DEUTERATED COMPOUNDS FOR TREATING FABRY, GAUCHER, PARKINSON'S AND RELATED DISEASES AND CONDITIONS, AND COMPOSITIONS AND METHODS THEREOF
    申请人:X-Cutag Therapeutics, Inc.
    公开号:US20190248790A1
    公开(公告)日:2019-08-15
    Novel deuterium-containing chemical compounds are provided. They are glucosylceramide (GSC) synthase inhibitors and are useful for treating various types of lysosomal storage diseases including Fabry's disease, Gaucher's disease and Parkinson's disease, or related diseases and conditions. Also described are pharmaceutical compositions, and methods of preparation and use thereof.
    提供了含的新型化学化合物。它们是葡萄糖酰胺(GSC)合成酶抑制剂,可用于治疗包括法布瑞氏病、高雪氏病和帕森病等各种类型的溶酶体贮积病,或相关疾病和症状。还描述了药物组合物以及其制备和使用方法。
  • METHOD OF PREPARING GLUCOSYLCERAMIDE SYNTHASE INHIBITORS
    申请人:Genzyme Corporation
    公开号:US20170334903A1
    公开(公告)日:2017-11-23
    The invention relates to a method of preparing inhibitors of glucosylceramide synthase (GCS) useful for the treatment metabolic diseases, such as lysosomal storage diseases, either alone or in combination with enzyme replacement therapy, and for the treatment of cancer.
    这项发明涉及一种制备葡萄糖鞘氨醇合成酶(GCS)抑制剂的方法,用于治疗代谢性疾病,如溶酶体贮积病,可以单独使用,也可以与酶替代疗法结合使用,并用于癌症治疗。
  • [EN] METHOD OF PREPARING GLUCOSYLCERAMIDE SYNTHASE INHIBITORS<br/>[FR] PROCÉDÉ DE PRÉPARATION D'INHIBITEURS DE LA GLUCOSYLCÉRAMIDE SYNTHASE
    申请人:GENZYME CORP
    公开号:WO2014151291A1
    公开(公告)日:2014-09-25
    The invention relates to a method of preparing inhibitors of glucosylceramide synthase (GCS) useful for the treatment metabolic diseases, such as lysosomal storage diseases, either alone or in combination with enzyme replacement therapy, and for the treatment of cancer.
    这项发明涉及一种制备葡糖鞘氨醇合成酶(GCS)抑制剂的方法,用于治疗代谢性疾病,如溶酶体贮积病,可以单独使用或与酶替代疗法结合使用,并用于癌症治疗。
  • [EN] SALT FORMS OF (S)-Quinuclidin-3-yl (2-(2-(4-fluorophenyl)thiazol-4-yl)propan-2-yl)carbamate<br/>[FR] FORMES DE SEL DE (S)-QUINUCLIDIN-3-YL (2-(2-(4-FLUOROPHÉNYL)THIAZOL-4-YL)PROPAN-2-YL)CARBAMATE
    申请人:GENZYME CORP
    公开号:WO2014152215A1
    公开(公告)日:2014-09-25
    The present invention relates to novel salt forms of (S)-Quinuclidin-3-yl (2-(2-(4-fluorophenyl)thiazol-4-yl)propan-2-yl)carbamate useful as an inhibitor of glucosylceramide synthase (GCS) and for the treatment metabolic diseases, such as lysosomal storage diseases, either alone or in combination with enzyme replacement therapy, and for the treatment of cancer.
    本发明涉及(S)-喹啉-3-基(2-(2-(4-氟苯基)噻唑-4-基)丙基)甲酸盐形式,用作葡糖鞘氨醇合成酶(GCS)的抑制剂,用于治疗代谢性疾病,如溶酶体贮积病,可单独使用或与酶替代疗法结合使用,并用于癌症的治疗。
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