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N-methylethanolamine phosphate | 6909-61-1

中文名称
——
中文别名
——
英文名称
N-methylethanolamine phosphate
英文别名
2-(methylamino)ethyl dihydrogen phosphate
N-methylethanolamine phosphate化学式
CAS
6909-61-1
化学式
C3H10NO4P
mdl
——
分子量
155.09
InChiKey
HZDCAHRLLXEQFY-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):
    -4.3
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    78.8
  • 氢给体数:
    3
  • 氢受体数:
    5

SDS

SDS:8674d8b64ed3d931c1eb83ac0850bd0a
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反应信息

  • 作为产物:
    描述:
    氢气 作用下, 以 甲醇 为溶剂, 反应 1.0h, 以84%的产率得到N-methylethanolamine phosphate
    参考文献:
    名称:
    Structurally diverse low molecular weight activators of the mammalian pre-mRNA 3′ cleavage reaction
    摘要:
    The 3' end formation of mammalian pre-mRNA contributes to gene expression regulation by setting the downstream boundary of the 3' untranslated region, which in many genes carries regulatory sequences. A large number of protein cleavage factors participate in this pre-mRNA processing step, but chemical tools to manipulate this process are lacking. Guided by a hypothesis that a PPM1 family phosphatase negatively regulates the 3' cleavage reaction, we have found a variety of new small molecule activators of the in vitro reconstituted pre-mRNA 3' cleavage reaction. New activators include a cyclic peptide PPM1D inhibitor, a dipeptide with modifications common to histone tails, abscisic acid and an improved L-arginine beta-naphthylamide analog. The minimal concentration required for in vitro cleavage has been improved from 200 mu M to the 200 nM-100 mu M range. These compounds provide unexpected leads in the search for small molecule tools able to affect pre-mRNA 3' end formation. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.12.006
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文献信息

  • Recherches sur la formation et la transformation des esters XIII. Sur la réaction des aminoalcools avec l'acide polyphosphorique:phosphorylation et/ou cyclisation
    作者:Emile Cherbuliez、J. Rabinowitz
    DOI:10.1002/hlca.19580410426
    日期:——
    In presence of pyro- or polyphosphoric acid at high temperature and low pressure, the aminoalkohols can undergo three types of reaction: (A) Phosphorylation, (B) Simultaneous phosphorylation and condensation, (C) Condensation.
    在高温和低压下存在焦磷酸或多磷酸的情况下,氨基醇会经历三种类型的反应:(A)磷酸化,(B)同时磷酸化和缩合,(C)缩合。
  • Fuchs, Zeitschrift fur Biologie (Munich), 1939, vol. 99, p. 298,300
    作者:Fuchs
    DOI:——
    日期:——
  • WOLF; NYC, Journal of Biological Chemistry, 1959, vol. 234, # 5, p. 1068 - 1071
    作者:WOLF、NYC
    DOI:——
    日期:——
  • Structurally diverse low molecular weight activators of the mammalian pre-mRNA 3′ cleavage reaction
    作者:Min Ting Liu、Nagaraja N. Nagre、Kevin Ryan
    DOI:10.1016/j.bmc.2013.12.006
    日期:2014.1
    The 3' end formation of mammalian pre-mRNA contributes to gene expression regulation by setting the downstream boundary of the 3' untranslated region, which in many genes carries regulatory sequences. A large number of protein cleavage factors participate in this pre-mRNA processing step, but chemical tools to manipulate this process are lacking. Guided by a hypothesis that a PPM1 family phosphatase negatively regulates the 3' cleavage reaction, we have found a variety of new small molecule activators of the in vitro reconstituted pre-mRNA 3' cleavage reaction. New activators include a cyclic peptide PPM1D inhibitor, a dipeptide with modifications common to histone tails, abscisic acid and an improved L-arginine beta-naphthylamide analog. The minimal concentration required for in vitro cleavage has been improved from 200 mu M to the 200 nM-100 mu M range. These compounds provide unexpected leads in the search for small molecule tools able to affect pre-mRNA 3' end formation. (C) 2013 Elsevier Ltd. All rights reserved.
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同类化合物

(11bR,11''bR)-2,2''-[氧双(亚甲基)]双[4-羟基-4,4''-二氧化物-二萘并[2,1-d:1'',2''-f][1,3,2]二氧磷杂七环 (11aR)-10,11,12,13-四氢-5-羟基-3,7-二-1-萘-5-氧化物-二茚基[7,1-de:1'',7''-fg][1,3,2]二氧杂磷杂八环 鲸蜡基磷酸-鲸蜡基磷酸二乙醇胺 非对称二乙基二(二甲基胺基)焦磷酸酯 雷公藤甲素O-甲基磷酸酯二苄酯 阿扎替派 间苯二酚双[二(2,6-二甲基苯基)磷酸酯] 锌四戊基二(磷酸酯) 银(1+)二苄基磷酸酯 铵4-(2-甲基-2-丁炔基)苯基4-(2-甲基-2-丙基)苯基磷酸酯 铵2-乙基己基磷酸氢酯 铵2,3-二溴丙基磷酸酯 钾二己基磷酸酯 钾二十烷基磷酸酯 钾二乙基磷酸酯 钾[5,7,7-三甲基-2-(1,3,3-三甲基丁基)辛基]磷酸酯 钾2-己基癸基磷酸酯 钴(2+)十三烷基磷酸酯 钡4,4-二乙氧基-2,3-二羟基丁基磷酸酯 钠辛基氢磷酸酯 钠癸基氢磷酸酯 钠异丁基氢磷酸酯 钠二苄基磷酸酯 钠二(2-丁氧乙基)磷酸酯 钠O,O-二乙基磷酰蔷薇l烯酸酯 钠4-氨基苯基氢磷酸酯水合物(1:1:1) 钠3,6,9,12,15-五氧杂二十八碳-1-基氢磷酸酯 钠2-乙氧基乙基磷酸酯 钠2,3-二溴丙基磷酸酯 钙敌畏 钙二钠氟-二氧代-氧代膦烷碳酸盐 钙3,9-二氧代-2,4,8,10-四氧杂-3lambda5,9lambda5-二磷杂螺[5.5]十一烷3,9-二氧化物 野尻霉素6-磷酸酯 酚酞单磷酸酯 酚酞单磷酸环己胺盐 酚酞二磷酸四钠盐 酚酞二磷酸四钠 辛基磷酸酯 辛基二氯膦酸酯 辛基二氯丙基磷酸酯 辛基二丙基磷酸酯 赤藓糖醇4-磷酸酯 螺[环丙烷-1,9-四环[3.3.1.02,4.06,8]壬烷],2-甲基-,(1-alpha-,2-ba-,4-ba-,5-alpha-,6-ba-,8-ba-)-(9CI) 蚜螨特 莽草酸-3-磷酸酯三钠盐 莽草酸-3-磷酸酯 苯酚,2,4-二硝基-,磷酸(酯)氢 苯氨基磷酸二乙酯 苯基二(2,4,6-三甲基苯基)磷酸酯 苯丁酰胺,N-(5-溴-2-吡啶基)-2,4-二甲基-α,γ-二羰基-