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NoName_910

中文名称
——
中文别名
——
英文名称
NoName_910
英文别名
2-(1-methylpiperidin-1-ium-1-yl)acetic acid
NoName_910化学式
CAS
——
化学式
C8H16NO2+
mdl
——
分子量
158.22
InChiKey
CRXFBHQGNFQOHL-UHFFFAOYSA-O
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):
    0.7
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Poly(ADP-ribose) polymerase 1 inhibitors structurally unrelated to NAD
    申请人:Institute for Cancer Research
    公开号:US10550108B2
    公开(公告)日:2020-02-04
    Compounds that are not related to NAD, and which target PARP1-histone H4 interaction are provided, as well as compositions of these compounds, and methods for specific inhibition of poly(ADP-ribose) polymerase 1 (PARP-1) using these compounds are provided. These PARP-1 inhibitors may be used to treat cancer in which PARP-1 activation or biologic activity plays a role, including prostate cancer, breast cancer, kidney cancer, ovarian cancer, lymphoma, leukemia, and glioblastoma, among others.
    本研究提供了与 NAD 无关的、针对 PARP1-组蛋白 H4 相互作用的化合物以及这些化合物的组合物,并提供了使用这些化合物特异性抑制聚(ADP-核糖)聚合酶 1(PARP-1)的方法。这些 PARP-1 抑制剂可用于治疗 PARP-1 活化或生物活性起作用的癌症,包括前列腺癌、乳腺癌、肾癌、卵巢癌、淋巴瘤、白血病和胶质母细胞瘤等。
  • EP3200792A2
    申请人:——
    公开号:EP3200792A2
    公开(公告)日:2017-08-09
  • Poly(ADP-Ribose) Polymerase 1 Inhibitors Structurally Unrelated to NAD
    申请人:Institute for Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center
    公开号:US20170283402A1
    公开(公告)日:2017-10-05
    Compounds that are not related to NAD, and which target PARP1-histone H4 interaction are provided, as well as compositions of these compounds, and methods for specific inhibition of poly(ADP-ribose) polymerase 1 (PARP-1) using these compounds are provided. These PARP-1 inhibitors may be used to treat cancer in which PARP-1 activation or biologic activity plays a role, including prostate cancer, breast cancer, kidney cancer, ovarian cancer, lymphoma, leukemia, and glioblastoma, among others.
  • [EN] NOVEL IONIC LIQUIDS<br/>[FR] NOUVEAUX LIQUIDES IONIQUES
    申请人:UNIV LEUVEN KATH
    公开号:WO2007147222A9
    公开(公告)日:2008-02-14
    [EN] The present invention provides for novel organic salts, more specifically ionic liquids and for methods for the preparation of such novel ionic liquids. The invention also provides for the use of the ionic liquids in chemistry applications, for example for the solubilization of metal oxides, hydroxides and salts, for the deposition of metals or for extraction procedures, among others. The invention furthermore provides for a method for the solubilization of metal oxides and metal salts, for the deposition of metals and for extraction procedures, this by using the novel ionic liquids. The present invention furthermore provides for materials obtained by the methods hereof.
    [FR] La présente invention concerne de nouveaux sels organiques, plus spécifiquement des liquides ioniques et les procédés de préparation de tels nouveaux liquides ioniques. L'invention concerne également l'utilisation des liquides ioniques dans des applications en chimie, par exemple, dans la solubilisation d'oxydes, d'hydroxydes et de sels métalliques, dans le dépôt de métaux ou dans des procédures d'extraction, entre autres. L'invention concerne, en outre, un procédé de solubilisation d'oxydes métalliques et de sels métalliques, de dépôt de métaux, le procédé s'appliquant aussi à des procédures d'extraction, ceci en utilisant les nouveaux liquides ioniques. La présente invention concerne, en outre, des matériaux obtenus par les présents procédés.
  • [EN] POLY (ADP-RIBOSE) POLYMERASE 1 INHIBITORS STRUCTURALLY UNRELATED TO NAD<br/>[FR] INHIBITEURS DE POLY(ADP-RIBOSE) POLYMÉRASE 1 STRUCTURELLEMENT NON APPARENTÉS À NAD
    申请人:INST CANCER RES D B A THE RES INST OF FOX CHASE CANCER CT
    公开号:WO2016054237A2
    公开(公告)日:2016-04-07
    Compounds that are not related to NAD, and which target PARPl-histone H4 interaction are provided, as well as compositions of these compounds, and methods for specific inhibition of poly(ADP-ribose) polymerase 1 (PARP-1) using these compounds are provided. These PARP-1 inhibitors may be used to treat cancer in which PARP-1 activation or biologic activity plays a role, including prostate cancer, breast cancer, kidney cancer, ovarian cancer, lymphoma, leukemia, and glioblastoma, among others.
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同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-N,3,3-三甲基-N-(苯甲基)丁酰胺 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素(1-6) 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸