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AAD 1154 | 478932-64-8

中文名称
——
中文别名
——
英文名称
AAD 1154
英文别名
N-[2-cyano-1-(2,5-dichlorophenoxy)propan-2-yl]-4-(trifluoromethoxy)benzamide
AAD 1154化学式
CAS
478932-64-8
化学式
C18H13Cl2F3N2O3
mdl
——
分子量
433.214
InChiKey
LCRHPJDLDGODHC-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):
    5.3
  • 重原子数:
    28
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    71.4
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

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文献信息

  • ANTICANCER AGENT COMPRISING AMINOACETONITRILE COMPOUND AS ACTIVE INGREDIENT
    申请人:NIHON NOHYAKU CO., LTD.
    公开号:US20160213640A1
    公开(公告)日:2016-07-28
    The present invention relates to an anticancer agent having a high safety and a superior anticancer activity, and an anticancer agent containing, as an active ingredient, an aminoacetonitrile compound represented by the formula (I) wherein R 1 is a hydrogen atom, an alkyl group and the like, R 2 , R 3 , and R 4 are the same or different and each is a hydrogen atom, an alkyl group and the like, R 5 and R 6 are the same or different and each is a hydrogen atom, a halogen atom and the like, m is 0 or 1, R is a halogen atom, a cyano group, a nitro group, a phenyl group optionally substituted by an alkyl group and the like, an alkyl group and the like, Ar 1 is a phenyl group, a naphthyl group, a pyridyl group, a pyrazolyl group, or the like, each of which is optionally substituted by a halogen atom, a cyano group, a nitro group, alkyl group and the like, and W is —O—, —S—, —SO 2 —, or —N(R 7 )— wherein R 7 is a hydrogen atom, a (C 1 -C 6 )alkyl group and the like, or a pharmacologically acceptable salt thereof.
    本发明涉及一种具有高安全性和优越抗癌活性的抗癌剂,以及一种含有氨基乙腈化合物作为活性成分的抗癌剂,所述氨基乙腈化合物由以下式(I)表示:其中R1为氢原子、烷基等,R2、R3和R4相同或不同,每个为氢原子、烷基等,R5和R6相同或不同,每个为氢原子、卤原子等,m为0或1,R为卤原子、基、硝基、苯基(可选择地由烷基取代)等,烷基等,Ar1为苯基、基、吡啶基、吡唑基等,每个均可选择地由卤原子、基、硝基、烷基等取代,W为—O—、—S—、—SO2—或—N(R7)—,其中R7为氢原子、(C1-C6)烷基等,或其药理学上可接受的盐。
  • [EN] ANTI CANCER AGENT COMPRISING AMINOACETONITRILE COMPOUND AS ACTIVE INGREDIENT<br/>[FR] AGENT ANTICANCÉREUX COMPRENANT UN COMPOSÉ D'AMINOACÉTONITRILE EN TANT QUE PRINCIPE ACTIF
    申请人:NIHON NOHYAKU CO LTD
    公开号:WO2016137010A1
    公开(公告)日:2016-09-01
    The present invention relates to an anticancer agent having a high safety and a superior anticancer activity, and anticancer agent containing, as an active ingredient, an aminoacetonitrile compound represented by the formula (I) wherein R1 is a hydrogen atom, an alkyl group and the like, R2, R3, and R4 are the same or different and each is a hydrogen atom, an alkyl group and the like, R5 and R6 are the same or different and each is a hydrogen atom, a halogen atom and the like, m is 0 or 1, R is a halogen atom, a cyano group, a nitro group, a phenyl group optionally substituted by an alkyl group and the like, an alkyl group and the like, Ar1 is a phenyl group, a naphthyl group, a pyridyl group, a pyrazolyl group, or the like, each of which is optionally substituted by a halogen atom, a cyano group, a nitro group, alkyl group and the like, and W is -O-, -S-, -SO2-, or -N(R7)- wherein R7 is a hydrogen atom, a (C1-C6) alkyl group and the like, or a pharmacologically acceptable salt thereof.
    本发明涉及一种具有高安全性和优越抗癌活性的抗癌药物,该抗癌药物含有作为活性成分的氨基乙腈化合物,其化学式表示为(I),其中R1是氢原子、烷基等,R2、R3和R4相同或不同,每个是氢原子、烷基等,R5和R6相同或不同,每个是氢原子、卤原子等,m为0或1,R是卤原子、基、硝基、苯基(可选择地由烷基取代)等,Ar1是苯基、基、吡啶基、吡唑基等,每个基可选择地由卤原子、基、硝基、烷基等取代,W是-O-、-S-、-SO2-或-N(R7)-,其中R7是氢原子、(C1-C6)烷基等,或其药理学上可接受的盐。
  • Amidoacetonitrile derivatives
    申请人:Gauvry Noelle
    公开号:US20070072944A1
    公开(公告)日:2007-03-29
    The invention relates to compounds of the general formula (I) wherein X, Y and W have the significances given in claim 1 and optionally the enantiomers thereof. The active ingredients have advantageous pesticidal properties. They are especially suitable for controlling parasites in and on warm-blooded animals.
    本发明涉及一般式(I)中X、Y和W具有权利要求1中所给出的意义及其对映异构体的化合物。这些活性成分具有优良的杀虫性能。它们特别适用于控制温血动物体内和体外的寄生虫。
  • Amidoacetonitrile Derivatives
    申请人:Gauvry Noelle
    公开号:US20090176868A1
    公开(公告)日:2009-07-09
    The invention relates to compounds of the general formula (I) wherein X, Y and W have the significances given in claim 1 and optionally the enantiomers thereof. The active ingredients have advantageous pesticidal properties. They are especially suitable for controlling parasites in and on warm-blooded animals.
    本发明涉及一般式(I)的化合物,其中X,Y和W具有权利要求1中给出的意义,且包括其对映体。这些活性成分具有优良的杀虫特性。它们特别适用于控制温血动物体内外的寄生虫。
  • KINASE INHIBITORS FOR THE TREATMENT OF CANCER
    申请人:Pitney Pharmaceuticals Pty Limited
    公开号:EP3061451A1
    公开(公告)日:2016-08-31
    The present invention relates to kinase inhibitors for the treatment of cancer. Specifically, the present invention relates to the use of aminoacetonitrile derivatives (AADs) in the treatment of cancer.
    本发明涉及用于治疗癌症的激酶抑制剂。具体来说,本发明涉及氨基乙腈生物AADs)在治疗癌症中的应用。
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