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3-hydroxy-1-(4-morpholinyl)-1-propanone | 28330-43-0

中文名称
——
中文别名
——
英文名称
3-hydroxy-1-(4-morpholinyl)-1-propanone
英文别名
4-(3-hydroxy-propionyl)-morpholine;3-Hydroxy-1-morpholin-4-ylpropan-1-one
3-hydroxy-1-(4-morpholinyl)-1-propanone化学式
CAS
28330-43-0
化学式
C7H13NO3
mdl
——
分子量
159.185
InChiKey
LRXAPWATGNQFKX-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:
    54-55 °C
  • 沸点:
    349.7±37.0 °C(Predicted)
  • 密度:
    1.189±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.4
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    49.8
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] METHODS OF TREATING ALZHEIMER'S DISEASE USING AROMATICALLY SUBSTITUTED omega-AMINO-ALKANOIC ACID AMIDES AND ALKANOIC ACID DIAMIDES<br/>[FR] METHODES DE TRAITEMENT DE LA MALADIE D'ALZHEIMER AU MOYEN D'AMIDES D'ACIDE O-AMINO-ALCANOIQUE A SUBSTITUTIONS AROMATIQUES ET DE DIAMIDES D'ACIDE ALCANOIQUE
    申请人:ELAN PHARM INC
    公开号:WO2003103652A1
    公开(公告)日:2003-12-18
    Disclosed.are methods for treating Alzheimer's disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting deposition of A beta peptide in a mammal, by use of compounds of formula (I) wherein the variables R1, R2, R3, R4, R5, X1, and X2 are defined herein.
    披露了治疗阿尔茨海默病和其他疾病,和/或抑制β-分泌酶酶,和/或通过使用式(I)化合物在哺乳动物体内抑制Aβ肽沉积的方法,其中变量R1、R2、R3、R4、R5、X1和X2在此处定义。
  • CATALYST FOR CONVERTING ESTER TO AMIDE USING HYDROXYL GROUP AS ORIENTATION GROUP
    申请人:CHUBU UNIVERSITY EDUCATIONAL FOUNDATION
    公开号:US20210070690A1
    公开(公告)日:2021-03-11
    Provided is a method for amidating a hydroxy ester compound at a high chemical selectivity. The amidation reaction method for a hydroxy ester compound comprises, in the presence of a catalyst containing a compound of a transition metal of the group 4 or group 5 in the periodic table, reacting at least one kind of hydroxy ester compound selected from the group consisting of an α-hydroxy ester compound, a β-hydroxy ester compound, a γ-hydroxy ester compound and a δ-hydroxy ester compound with an amino compound so as to amidate an ester group having a hydroxyl group at the α-, β-, γ- or δ-position of the hydroxy ester compound.
    提供了一种在高化学选择��下对羟基酯化合物进行酰胺化的方法。对羟基酯化合物进行酰胺化反应的方法包括,在含有周期表中第4组或第5组过渡属化合物的催化剂存在下,将从α-羟基酯化合物、β-羟基酯化合物、γ-羟基酯化合物和δ-羟基酯化合物组成的羟基酯化合物中选择的至少一种羟基酯化合物与氨基化合物反应,以酰胺化具有α-、β-、γ-或δ-位置的羟基酯化合物中的羟基基团。
  • Methods of treating alzheimer's disease using aromatically substituted w-amino-alkanoic acid amides and alkanoic acid diamides
    申请人:Maillard Michel
    公开号:US20060089355A1
    公开(公告)日:2006-04-27
    Disclosed are methods for treating Alzheimer's disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting de-position of A beta peptide in a mammal, by use of compounds of formula (I) wherein the variables R 1 , R 2 , R 3 , R 4 , R 5 , X 1 , and X 2 are defined herein.
    本发明涉及使用式(I)中的化合物治疗阿尔茨海默病和其他疾病,抑制β-秘鲁酶的活性,抑制Aβ肽在哺乳动物体内的沉积。其中,变量R1、R2、R3、R4、R5、X1和X2的定义如下。
  • Methods of treating alzheimer's disease
    申请人:Schostarez Heinrich
    公开号:US20050130941A1
    公开(公告)日:2005-06-16
    Disclosed are methods for treating Alzheimer's disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting deposition of A beta peptide in a mammal, by use of hydrazine compounds of formula (I) wherein the variables R 1 -R 9 are defined herein.
    本发明涉及使用式(I)中变量R1-R9所定义的化合物治疗阿尔茨海默病和其他疾病,抑制β-分泌酶酶活性,抑制A beta肽在哺乳动物体内的沉积。
  • Hydrazone derivative
    申请人:Kawagoe Keiichi
    公开号:US20060276433A1
    公开(公告)日:2006-12-07
    A compound represented by the following formula (I): wherein R 1 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R 2 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R 3 represents hydrogen, etc.; Ar represents a divalent group derived from aromatic hydrocarbon, etc.; X represents a single bond, linear or branched alkylene having from 1 to 3 carbon atoms which may have a substituent, etc.; and G represents halogen, a saturated or unsaturated 5- or 6-membered cyclic hydrocarbon group which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc., a salt thereof or a solvate thereof; and an agent for inhibiting aggregation and/or deposition of an amyloid protein or an amyloid-like protein, which comprises the compound, a salt thereof or a solvate thereof.
    以下是式子(I)所代表的化合物: 其中,R1代表氢、芳基(可能带有取代基)、饱和或不饱和的5-至7-成员杂环基(可能带有取代基)等; R2代表氢、芳基(可能带有取代基)、饱和或不饱和的5-至7-成员杂环基(可能带有取代基)等; R3代表氢等; Ar代表从芳香族碳氢化合物衍生的二价基团等; X代表单键、线性或支链烷基,具有1至3个碳原子,可能带有取代基等; G代表卤素、饱和或不饱和的5-或6-成员环烃基(可能带有取代基)、饱和或不饱和的5-至7-成员杂环基(可能带有取代基)等,其盐或溶剂化物;以及用于抑制淀粉样蛋白或类淀粉样蛋白的聚集和/或沉积的药剂,包括该化合物、其盐或溶剂化物。
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