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克罗乙胺 | 6168-76-9

中文名称
克罗乙胺
中文别名
——
英文名称
crotetamide
英文别名
n-[1-(Dimethylamino)-1-oxobutan-2-yl]-n-ethylbut-2-enamide;2-[but-2-enoyl(ethyl)amino]-N,N-dimethylbutanamide
克罗乙胺化学式
CAS
6168-76-9
化学式
C12H22N2O2
mdl
——
分子量
226.319
InChiKey
LSAMUAYPDHUBQD-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

物化性质

  • 熔点:
    <25 °C
  • 沸点:
    bp0.03 132-134°
  • 密度:
    0.986±0.06 g/cm3(Predicted)
  • 溶解度:
    氯仿(微溶)、乙酸乙酯(微溶)、甲醇(微溶)

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2924199090

反应信息

  • 作为产物:
    描述:
    DL-2-crotonoylamino-butyric acid dimethylamide 在 sodium amide 、 xylene 作用下, 生成 克罗乙胺
    参考文献:
    名称:
    CH244952
    摘要:
    公开号:
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文献信息

  • CYCLODEXTRIN-BASED POLYMERS FOR THERAPEUTIC DELIVERY
    申请人:Cerulean Pharma Inc.
    公开号:US20130196906A1
    公开(公告)日:2013-08-01
    Provided are methods relating to the use of CDP-therapeutic agent conjugates for the treatment of a disease or disorder, e.g., autoimmune disease, inflammatory disease, central nervous system disorder, cardiovascular disease, or metabolic disorder. Also provided are CDP-therapeutic agent conjugates, particles comprising CDP-therapeutic agent conjugates, and compositions comprising CDP-therapeutic agent conjugates.
    提供了关于使用CDP-治疗剂偶联物治疗疾病或紊乱的方法,例如自身免疫疾病、炎症性疾病、中枢神经系统紊乱、心血管疾病或代谢紊乱。还提供了CDP-治疗剂偶联物、包含CDP-治疗剂偶联物的颗粒以及包含CDP-治疗剂偶联物的组合物。
  • COMPOSITIONS AND METHODS FOR TREATMENT OF AUTOIMMUNE AND OTHER DISEASE
    申请人:CERULEAN PHARMA INC.
    公开号:US20180193486A1
    公开(公告)日:2018-07-12
    Provided are methods relating to the use of CDP-therapeutic agent conjugates for the treatment of autoimmune disease, inflammatory disease, or cancer. Also provided are CDP-therapeutic agent conjugates, particles comprising CDP-therapeutic agent conjugates, and compositions comprising CDP-therapeutic agent conjugates.
    提供了关于使用CDP-治疗剂偶联物治疗自身免疫疾病、炎症性疾病或癌症的方法。还提供了CDP-治疗剂偶联物、包含CDP-治疗剂偶联物的颗粒以及包含CDP-治疗剂偶联物的组合物。
  • Hydroxylated nebivolol metabolites
    申请人:O'Donnell P. John
    公开号:US20070014733A1
    公开(公告)日:2007-01-18
    Hydroxylated nebivolol metabolites increase NO release from human endothelial cell preparations in a concentration dependent fashion following acute administration. In addition, hydroxylated nebivolol metabolites, including but not limited to 4-hydroxy-6,6′difluoro-, 4-hydroxy-5-phenol-6,6′difluoro-, and 4-hydroxy-8-pheno-6,6′difluoro-, have the ability to increase the capacity for NO release in human endothelial cells following chronic administration. This invention provides hydroxylated nebivolol metabolites and compositions comprising nebivolol and/or at least one hydroxylated metabolite of nebivolol and/or at least one additional compound used to treat cardiovascular diseases or a pharmaceutically acceptable salt thereof. In addition, this invention provides methods of treating and/or preventing vascular diseases by administering at least one hydroxylated metabolite of nebivolol that is capable of releasing a therapeutically effective amount of nitric oxide to a targeted site affected by the vascular disease. Also, this invention is directed to the treatment and/or prevention of migraine headaches administering at least one hydroxylated metabolite of nebivolol. This invention may also be used in conjunction with or as a single treatment of metabolic syndrome disorders.
    羟基化奈必洛尔代谢物在急性给药后以浓度依赖性方式增加人内皮细胞制剂的一氧化氮释放。此外,羟基化奈必洛尔代谢物,包括但不限于4-羟基-6,6'-二氟代-、4-羟基-5-苯酚-6,6'-二氟代-和4-羟基-8-苯并-6,6'-二氟代-,在慢性给药后能够增加人内皮细胞的一氧化氮释放能力。本发明提供了羟基化奈必洛尔代谢物和包含奈必洛尔和/或至少一种羟基化奈必洛尔代谢物和/或至少一种用于治疗心血管疾病的附加化合物的组合物,以及可药用的盐。此外,本发明还提供了通过给药至少一种能够释放治疗有效量的一氧化氮到受血管疾病影响的靶向部位的羟基化奈必洛尔代谢物来治疗和/或预防血管疾病的方法。本发明还涉及通过给药至少一种羟基化奈必洛尔代谢物来治疗和/或预防偏头痛。本发明还可以与治疗代谢综合征障碍的其他治疗联合使用,或作为单一治疗。
  • [EN] 3-(PYRIDIN-3-YL)-ACRYLAMIDE AND N-(PYRIDIN-3-YL)-ACRYLAMIDE DERIVATIVES AND THEIR USE AS PAK OR NAMPT MODULATORS<br/>[FR] DÉRIVÉS 3-(PYRIDIN-3-YL)-ACRYLAMIDE ET N-(PYRIDIN-3-YL)-ACRYLAMIDE ET LEUR UTILISATION COMME MODULATEURS DE PAK OU NAMPT
    申请人:KARYOPHARM THERAPEUTICS INC
    公开号:WO2017031213A1
    公开(公告)日:2017-02-23
    The invention generally relates to cyclic compounds and, more particularly, to a compound represented by Structural Formula I: or a pharmaceutically acceptable salt thereof and pharmaceutical compositions comprising the multicyclic compounds. The invention also relates to a method for treating a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T- Cell mediated autoimmune diseases) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.
    该发明通常涉及环状化合物,更具体地涉及由结构式I表示的化合物:或其药学上可接受的盐以及包含多环化合物的药物组合物。该发明还涉及一种治疗癌症(例如淋巴瘤,如边缘区淋巴瘤)、神经退行性疾病、炎症性疾病或免疫系统疾病(例如T细胞介导的自身免疫疾病)的方法,该方法包括向需要的受试者施用该发明的化合物或其药学上可接受的盐的治疗有效量,或者包括该发明的化合物或其药学上可接受的盐的组合物。
  • [EN] CYCLIC COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS CYCLIQUES ET LEURS UTILISATIONS
    申请人:KARYOPHARM THERAPEUTICS INC
    公开号:WO2016100515A1
    公开(公告)日:2016-06-23
    The invention generally relates to substituted benzothiophenyl, substituted benzothiazolyl, substituted indolyl and substituted benzoimidazolyl compounds and, more particularly, to a compound represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, inflammatory diseases or an autoimmune system disease (e.g., a T-Cell mediated autoimmune disesase).
    该发明通常涉及取代苯并噻吩基、取代苯并噻唑基、取代吲哚基和取代苯并咪唑基化合物,更具体地,涉及一种由结构式I表示的化合物或其药学上可接受的盐,其中变量如本文所定义和描述。该发明还包括合成和使用结构式I的化合物,或其药学上可接受的盐或组合物,例如,在治疗癌症(例如淋巴瘤,如袍细胞淋巴瘤)、神经退行性疾病、炎症性疾病或自身免疫系统疾病(例如T细胞介导的自身免疫疾病)中的应用。
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