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N-(2-dimethylamino-ethyl)-isovaleramide | 72080-80-9

中文名称
——
中文别名
——
英文名称
N-(2-dimethylamino-ethyl)-isovaleramide
英文别名
N-(2-Dimethylamino-aethyl)-isovaleramid;N-[2-(dimethylamino)ethyl]-3-methylbutanamide
<i>N</i>-(2-dimethylamino-ethyl)-isovaleramide化学式
CAS
72080-80-9
化学式
C9H20N2O
mdl
MFCD03208878
分子量
172.271
InChiKey
SAVWJXVYYHDBHZ-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):
    0.8
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.888
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Viral Polymerase Inhibitors
    申请人:Beaulieu L. Pierre
    公开号:US20080045516A1
    公开(公告)日:2008-02-21
    Compounds of formula I: wherein X, R 2 , R 3 , R 5 and R 6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.
    式I的化合物: 其中X,R2,R3,R5和R6如本文所定义,可用作乙型肝炎病毒NS5B聚合酶的抑制剂。
  • Sulfonyl amide inhibitors of calcium channel function
    申请人:Hangeland J. Jon
    公开号:US20050245535A1
    公开(公告)日:2005-11-03
    Compounds of formula I its stereoisomers, solvates, and salts, thereof, wherein: a, b, c, d, f, n, m and Ra are defined herein are are inhibitors of calcium channel function, and are useful in treating calcium channel-dependent disorders, including hypertension.
    化合物I的立体异构体、溶剂合物和盐类,其中:a、b、c、d、f、n、m和Ra的定义如下,是钙通道功能的抑制剂,并且在治疗依赖于钙通道的疾病,包括高血压方面具有用处。
  • Quinazoline Derivatives Having Tyrosine Kinase Inhibitory Activity
    申请人:Kume Masaharu
    公开号:US20090143414A1
    公开(公告)日:2009-06-04
    A compound which inhibits both of EGF receptor tyrosine kinase and HER2 tyrosine kinase is provided. A compound represented by the general formula (I): wherein R X is a group represented by the formula: wherein R 1 is a hydrogen atom, optionally substituted alkyl, etc.; Z is —O—, —N(R 10 )—, etc.; R 10 is a hydrogen atom, alkyl, etc.; R 2 is a hydrogen atom, optionally substituted alkyl, etc.; R 18 is a hydrogen atom, optionally substituted alkyl, etc.; R 19 is optionally substituted alkyl, etc.; W 1 is an optionally substituted non-aromatic nitrogen-containing group; R 17 is a hydrogen atom, optionally substituted alkyl, etc.; R 3 and R 4 are independently a hydrogen atom, optionally substituted alkyl, etc.; X is —O—, —S—, or —N(R 12 )—, etc.; R 12 is a hydrogen atom, alkyl, etc.; and A is phenyl optionally having a substituent, etc., its pharmaceutically acceptable salt, or a solvate thereof.
    提供了一种抑制EGF受体酪氨酸激酶和HER2酪氨酸激酶的化合物。该化合物由通式(I)表示:其中RX是由以下式子表示的基团:其中R1是氢原子,可选取代烷基等;Z是—O—,—N(R10)—等;R10是氢原子,烷基等;R2是氢原子,可选取代烷基等;R18是氢原子,可选取代烷基等;R19是可选取代烷基等;W1是可选取代非芳香族含氮基团;R17是氢原子,可选取代烷基等;R3和R4分别是氢原子,可选取代烷基等;X是—O—,—S—或—N(R12)—等;R12是氢原子,烷基等;A是苯基,可选取代基等,其药物可接受的盐或其溶剂化合物。
  • ALPHA-(N-SULFONAMIDO)ACETAMIDE DERIVATIVES AS BETA-AMYLOID INHIBITORS
    申请人:Parker F. Michael
    公开号:US20080085894A1
    公开(公告)日:2008-04-10
    There is provided a series of novel α-(N-sulfonamido)acetamide compounds of the Formula (I) wherein R, R 1 , R 2 and R 3 are defined herein, which are inhibitors of β-amyloid peptide (β-AP) production and are useful in the treatment of Alzheimer's Disease and other conditions affected by anti-amyloid activity.
    提供了一系列新型α-(N-磺酰胺基)乙酰胺化合物的公式(I),其中R、R1、R2和R3在此定义,它们是β-淀粉样肽(β-AP)产生的抑制剂,并且在治疗阿尔茨海默病和其他受到抗淀粉样蛋白活性影响的疾病中有用。
  • NEW COMPOUNDS, PHARMACEUTICAL COMPOSITION AND METHODS RELATING THERETO
    申请人:DYCK Brian
    公开号:US20110166116A1
    公开(公告)日:2011-07-07
    New compounds are disclosed which have utility in the treatment of a variety of metabolic related conditions in a patient. The compounds of this invention have the structure (I): wherein R 1 , R 2 , R 3 , n, p, q, and Ar are as defined herein, including stereoisomers, and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions comprising a compound of this invention, as well as methods relating to the use thereof in a patient in need thereof.
    本发明披露了一种新化合物,其在治疗患者的各种代谢相关疾病方面具有用途。本发明的化合物具有结构(I):其中R1、R2、R3、n、p、q和Ar的定义如本文所述,包括立体异构体和药物可接受的盐。本发明还披露了包括本发明化合物的制药组合物,以及与在需要时使用该化合物的相关方法。
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