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N-(2-fluorophenyl)butanamide

中文名称
——
中文别名
——
英文名称
N-(2-fluorophenyl)butanamide
英文别名
——
N-(2-fluorophenyl)butanamide化学式
CAS
——
化学式
C10H12FNO
mdl
MFCD03062082
分子量
181.21
InChiKey
GVVLLAXPIWLPHM-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):
    1.8
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Inhibitors of VEGF receptor and HGF receptor signaling
    申请人:Saavedra Mario Oscar
    公开号:US20070004675A1
    公开(公告)日:2007-01-04
    The invention relates to the inhibition of VEGF receptor signaling and HGF receptor signaling. The invention provides compounds and methods for inhibiting VEGF receptor signaling and HGF receptor signaling. The invention also provides compositions and methods for treating cell proliferative diseases and conditions
    该发明涉及抑制VEGF受体信号和HGF受体信号。该发明提供了抑制VEGF受体信号和HGF受体信号的化合物和方法。该发明还提供了治疗细胞增殖性疾病和病况的组合物和方法。
  • [EN] TETRAHYDROQUINOLONES AND AZA-ANALOGUES THEREOF FOR USE AS DPP-IV INHIBITORS IN THE TREATEMENT OF DIABETES<br/>[FR] TETRAHYDROQUINOLONES ET AZA-ANALOGUES ASSOCIES UTILISES EN TANT QU'INHIBITEURS DE LA DPP-IV DANS LE TRAITEMENT DU DIABETE
    申请人:ASTRAZENECA AB
    公开号:WO2005123685A1
    公开(公告)日:2005-12-29
    Compound of formula (I) or a pharmaceutically-acceptable salt thereof, formula (I) wherein Ar is optionally substituted phenyl; R1 is selected from: formula a) or b) (wherein is a single or double bond); R5, R6, R7 and R8 are for example hydrogen or alkyl; R4 is selected from hydrogen, (3-4C)cycloalkyl and optionally substituted (1-4C)alkyl; R10 is for example selected from hydrogen, (1-4C)alkyl, (3-6C)cycloalkyl(1-4C)alkyl, hydroxy(1-4C)alkyl, (1-4C)alkoxy, aryl(1-4C)alkyl; Y is carbon and Ring A is optionally substituted phenylene; or each Y may independently be carbon or nitrogen and Ring A is optionally substituted 5- or 6-membered, heteroarylene ring; R11 is selected from hydrogen and optionally substituted phenyl; p is independently at each occurrence 0, 1 or 2; are described. Processes for making such compounds and their use as DPP-IV inhibitors in the treatment of diabetes are also described.
    化合物的化学式(I)或其药用可接受的盐,其中化学式(I)中Ar是可选择的取代苯基;R1选自:化学式a)或b)(其中是单键或双键);R5、R6、R7和R8例如是氢或烷基;R4选自氢、(3-4C)环烷基和可选择的取代(1-4C)烷基;R10例如选自氢、(1-4C)烷基、(3-6C)环烷基(1-4C)烷基、羟基(1-4C)烷基、(1-4C)烷氧基、芳基(1-4C)烷基;Y是碳,环A是可选择的取代苯基;或每个Y可以独立地是碳或氮,环A是可选择的取代的5-或6-成员的杂芳烃环;R11选自氢和可选择的取代苯基;p在每次出现时独立地为0、1或2;描述了制备这类化合物的过程以及它们作为DPP-IV抑制剂在糖尿病治疗中的用途。
  • COMPOUNDS FOR THE TREATMENT OF CANCER AND INFLAMMATORY DISEASE
    申请人:SHY Therapeutics LLC
    公开号:US20170174699A1
    公开(公告)日:2017-06-22
    Provided herein are compounds that inhibit the phosphorylation of MAPK and thus are useful in compositions and methods for treating cancer and inflammatory disease.
    本文提供了抑制MAPK磷酸化的化合物,因此可用于治疗癌症和炎症性疾病的组合物和方法。
  • INHIBITORS OF VEGF RECEPTOR AND HGF RECEPTOR SIGNALING
    申请人:Saavedra Oscar Mario
    公开号:US20120083482A1
    公开(公告)日:2012-04-05
    The invention relates to the inhibition of VEGF receptor signaling and HGF receptor signaling. The invention provides compounds of general formula (A) wherein A 1 is sulfur, A 3 is CH, A 2 is CH, D is heterocycle, Z is oxygen, SO 0-2 or NR, Ar is phenyl and G is not a ring, and methods for inhibiting VEGF receptor signaling and HGF receptor signaling. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.
    本发明涉及抑制VEGF受体信号和HGF受体信号的技术。本发明提供了通式(A)的化合物,其中A1为,A3为CH,A2为CH,D为杂环,Z为氧,SO0-2或NR,Ar为苯基,G不是环,并提供了抑制VEGF受体信号和HGF受体信号的方法。本发明还提供了治疗细胞增殖性疾病和病情的组合物和方法。
  • Method of catalytic crosslinking of polymers and two-pack composition used therein
    申请人:ROHM AND HAAS COMPANY
    公开号:EP0950669A2
    公开(公告)日:1999-10-20
    A method of crosslinking an oxidative polymer having oxidatively crosslinkable functional groups and a two-pack composition used therein. The oxidatively crosslinkable functional groups on the oxidative polymer are crosslinked by contacting the oxidative polymer with a catalytic amount of an oxidizing enzyme, such as horseradish peroxidase. The present invention is further directed to a two-pack coating composition which includes a polymeric component and a catalytic component, which are mixed together prior to use.
    一种交联具有可氧化交联官能团的氧化聚合物及其所用双组分组合物的方法。通过将氧化聚合物与催化量的氧化酶(如辣根过氧化物酶)接触,使氧化聚合物上的可氧化交联官能团交联。本发明还涉及一种双包装涂层组合物,它包括一种聚合物成分和一种催化成分,在使用前将它们混合在一起。
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