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N-(triethylammoniumsulfonyl)carbamate

中文名称
——
中文别名
——
英文名称
N-(triethylammoniumsulfonyl)carbamate
英文别名
N-(triethylazaniumyl)sulfonylcarbamate
N-(triethylammoniumsulfonyl)carbamate化学式
CAS
——
化学式
C7H16N2O4S
mdl
——
分子量
224.28
InChiKey
JHTJPSCVBLCXEO-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:
    14
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    94.7
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • [EN] MACROCYCLIC COMPOUNDS FOR INHIBITION OF INHIBITORS OF APOPTOSIS<br/>[FR] COMPOSÉS MACROCYCLIQUES POUR L'INHIBITION D'INHIBITEURS DE L'APOPTOSE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2014074658A1
    公开(公告)日:2014-05-15
    There are disclosed compounds that modulate the activity of inhibitors of apoptosis (IAPs), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders and disorders of dysregulated apoptosis, such as cancer, utilizing the compounds of the invention.
    这里公开了调节凋亡抑制剂(IAPs)活性的化合物,包含所述化合物的药物组合物以及使用本发明的化合物治疗增殖性疾病和凋亡失调疾病的方法,例如癌症。
  • MACROCYCLIC COMPOUNDS FOR INHIBITION OF INHIBITORS OF APOPTOSIS
    申请人:Ensemble Therapeutics Corp.
    公开号:US20140135270A1
    公开(公告)日:2014-05-15
    There are disclosed compounds that modulate the activity of inhibitors of apoptosis (IAPs), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders and disorders of dysregulated apoptosis, such as cancer, utilizing the compounds of the invention.
    这里公开了调节凋亡抑制剂(IAPs)活性的化合物,包含所述化合物的药物组合物以及使用本发明的化合物治疗增殖性疾病和凋亡失调疾病的方法,例如癌症。
  • [EN] ALKYNYL ALCOHOLS AND METHODS OF USE<br/>[FR] ALCOOLS D'ALCYNYLE ET PROCÉDÉS D'UTILISATION CORRESPONDANTS
    申请人:HOFFMANN LA ROCHE
    公开号:WO2015025025A1
    公开(公告)日:2015-02-26
    The invention relates to compounds of Formula (0): wherein Q, A1-A8, R4 and R5 and each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over- activation of NF-kB signaling is observed.
    这项发明涉及以下式的化合物(0):其中Q,A1-A8,R4和R5分别具有如本文所述的含义。式(0)的化合物及其药物组成物在治疗观察到NF-kB信号通路的不良或过度活化的疾病和紊乱中是有用的。
  • [EN] PIPERIDINYLPYRAZOLOPYRIMIDINONES AND THEIR USE<br/>[FR] PIPÉRIDINYLPYRAZOLOPYRIMIDINONES ET LEUR UTILISATION
    申请人:BAYER PHARMA AG
    公开号:WO2016071216A1
    公开(公告)日:2016-05-12
    The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.
    本申请涉及新型取代哌啶基吡唑嘧啶酮,以及它们的制备方法,这些化合物可单独或组合使用于治疗和/或预防疾病的方法中,特别是用于治疗和/或预防患有或不患有基础遗传或获得性止血障碍的患者的急性和复发性出血,其中出血与从重经期出血、产后出血、出血性休克、出血性膀胱炎、胃肠道出血、创伤、手术、移植、中风、肝脏疾病、遗传性血管性肿、鼻血、以及血液积聚后的滑膜炎和软骨损伤等一组疾病或医疗干预有关。
  • [EN] TRICYCLIC SUBSTITUTED THIADIAZINE DIOXIDE COMPOUNDS AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE<br/>[FR] COMPOSÉS DE DIOXYDE DE THIADIAZINE SUBSTITUÉS TRICYCLIQUES EN TANT QU'INHIBITEURS DE BACE, COMPOSITIONS ET LEUR UTILISATION
    申请人:MERCK SHARP & DOHME
    公开号:WO2014062549A1
    公开(公告)日:2014-04-24
    In its many embodiments, the present invention provides provides certain iminothiazine dioxide compounds, including compounds Formula (I): and tautomers and stereoisomers thereof, and pharmaceutically acceptable salts of said compounds, said tautomeros and said stereoisomers, wherein the middle ring (referred to herein as "ring B") of the tricyclic substituent is an optionally substituted 5-membered ring, and each of the remaining variables shown in the formula are as defined herein. The novel compounds of the invention are useful as BACE inhibitors and/or for the treatment and prevention of various pathologies related thereto. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use, including Alzheimer's disease, are also disclosed.
    在其多种实施方式中,本发明提供了某些亚噻唑二氧化物化合物,包括化合物式(I):及其互变异构体和立体异构体,以及所述化合物的药学上可接受的盐,所述互变异构体和所述立体异构体,其中三环取代基的中间环(以下简称为“环B”)是一个可选择取代的5-成员环,并且所示公式中的其余各变量如本文所定义。本发明的新化合物可用作BACE抑制剂和/或用于治疗和预防与之相关的各种病理。还公开了包括一种或多种此类化合物(单独和与一种或多种其他活性剂组合)的药物组合物,以及其制备和使用方法,包括治疗阿尔茨海默病。
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