摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[1,2]Oxazolo[4,5-b]pyridin-7-amine

中文名称
——
中文别名
——
英文名称
[1,2]Oxazolo[4,5-b]pyridin-7-amine
英文别名
[1,2]oxazolo[4,5-b]pyridin-7-amine
[1,2]Oxazolo[4,5-b]pyridin-7-amine化学式
CAS
——
化学式
C6H5N3O
mdl
——
分子量
135.12
InChiKey
VEFILPQJQRHUBK-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
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    64.9
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Heterocyclic inhibitors of MEK and methods of use thereof
    申请人:Wallace Eli
    公开号:US20050153942A1
    公开(公告)日:2005-07-14
    Disclosed are compounds of the Formula I and pharmaceutically acceptable salts and prodrugs thereof, wherein R 1 , R 2 , R 7 , R 8 and R 9 , W, X, Y and Z are as defined in the specification. Such compounds are MEK inhibitors and are useful in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals, and inflammatory conditions. Also disclosed are methods of using such compounds in the treatment of hyperproliferative diseases in mammals and pharmaceutical compositions containing such compounds.
    本发明涉及公式I的化合物及其药学上可接受的盐和前药,其中R1、R2、R7、R8和R9、W、X、Y和Z如规范中所定义。这些化合物是MEK抑制剂,可用于治疗哺乳动物的增殖过度疾病,如癌症和炎症,以及炎症病症。本发明还涉及使用这些化合物治疗哺乳动物的增殖过度疾病的方法和含有这些化合物的制药组合物。
  • EP1689406A4
    申请人:——
    公开号:EP1689406A4
    公开(公告)日:2007-01-17
  • HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF
    申请人:Array Biopharma, Inc.
    公开号:EP1689406A2
    公开(公告)日:2006-08-16
  • US7576072B2
    申请人:——
    公开号:US7576072B2
    公开(公告)日:2009-08-18
  • [EN] HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF<br/>[FR] INHIBITEURS HETEROCYCLIQUES DE MEK ET METHODES D'UTILISATION ASSOCIEES
    申请人:ARRAY BIOPHARMA INC
    公开号:WO2005051906A2
    公开(公告)日:2005-06-09
    Disclosed are compounds of the Formula I and pharmaceutically acceptable salts and prodrugs thereof, wherein R1, R2, R7, R8 and R9, W, X, Y and Z are as defined in the specification. Such compounds are MEK inhibitors and are useful in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals, and inflammatory conditions. Also disclosed are methods of using such compounds in the treatment of hyperproliferative diseases in mammals and pharmaceutical compositions containing such compounds.
查看更多

同类化合物

苯胺,4-肼基-3-甲氧基-N-苯基- 环丁[b][1,2]恶唑并[4,5-e]吡啶 异恶唑并[5,4-B]吡啶-3-胺 异噁唑并[5,4-c]吡啶-3-胺 异噁唑并[5,4-b]吡啶-3-醇 异噁唑并[4,5-b]吡啶-3-胺 异噁唑并[4,5-b]吡啶-3(2H)-酮 [1,2]恶唑并[5,4-e]吲嗪 9-氧杂-3-氮杂三环[5.2.1.03,8]癸-1,5,7-三烯 7H-[1,3]恶唑并[3,2-a]环氧乙烷并[d]吡啶 7-羟基-3-甲基[1,2]恶唑并[4,5-b]吡啶-5(4H)-酮 6-甲氧基-3-甲基[1,2]恶唑并[4,5-c]吡啶 5-肼基-3-甲基[1,2]恶唑并[4,5-b]吡啶 5-乙基-3-甲基[1,2]恶唑并[5,4-b]吡啶 5-乙基-3-甲基[1,2]恶唑并[4,5-b]吡啶 5,7-二氯-3-甲基异噁唑并[4,5-B]吡啶 4-甲氧基-3-甲基[1,2]恶唑并[5,4-b]吡啶 4-氧杂-7-氮杂三环[4.3.1.03,7]癸-1(9),2,5-三烯 4,6-二甲基异噁唑(5,4-B)吡啶-3-胺 3-甲基异噁唑并[5,4-b]吡啶 3-甲基[1,2]恶唑并[5,4-b]吡啶-5-甲酰氯 3-甲基[1,2]恶唑并[4,5-b]吡啶2-氧化物 3-甲基-6-噻吩-2-基异恶唑并[5,4-b]吡啶-4-羧酸 3-溴异噁唑并[5,4-B]吡啶 3-氨基异恶唑[4,5-C]并吡啶 3-(溴甲基)异噁唑并[5,4-B]吡啶 3-(1,3-苯并二恶唑-5-基)-N-[(1S)-1-苯乙基]-异唑并[5,4-c]吡啶-5-胺 3,6-二甲基[1,2]恶唑并[5,4-b]吡啶 2H-环戊二烯并[d]异噻唑并[5,4-b]吡啶(9CI) 2H-环戊二烯并[b][1,2]恶唑并[4,5-e]吡啶 2H-[1,2]恶唑并[5,4-b]吡咯并[3,4-D]吡啶 2-氯-N-异噁唑并[5,4-B]吡啶-3-基乙酰胺 1H-咪唑,1-丁基-2,5-二氢-2-(1-甲基乙基)- 6-(benzo[d][1,3]dioxol-5-yl)-5-methyl-3-phenylisoxazolo[4,5-c]pyridin-4(5H)-one 5-chloro-4,6-dimethylisoxazolo[5,4-b]pyridin-3-amine Isoxazolo[5,4-C]pyridine Isoxazolo[4,5-B]pyridine 3,5,6-trimethyl-7-nitroisoxazolo[4,5-b]pyridine-N-oxide 7-chloro-5-ethyl-3-methylisoxazolo<4,5-b>pyridine 5-Isopropyl-3,6-dimethyl-isoxazolo[4,5-b]pyridine 4-oxide N-(1-(4-(Trifluoromethylthio)phenyl)-ethyl)-isoxazolo[4,5-c]pyridin-3-amine isoxazolo[5,4-b]pyridine-3,4,6-triamine 3-isoxazolo[5,4-b]pyridin-3-yl-phenol (R)-1-(benzyl-methyl-amino)-3-(3-isoxazolo[5,4-b]pyridin-3-yl-phenoxy)-propan-2-ol (R)-1-benzylamino-3-(3-isoxazolo[5,4-b]pyridin-3-yl-phenoxy)-propan-2-ol (R)-1-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-3-(3-isoxazolo[5,4-b]pyridin-3-yl-phenoxy)-propan-2-ol (R)-1-[4-(3-chloro-phenoxy)-piperidin-1-yl]-3-(3-isoxazolo[5,4-b]pyridin-3-yl-phenoxy)-propan-2-ol ethyl 4,7-dihydro-3-methyl-4-oxo-7-pentylisoxazolo[5,4-b]pyridine-5-carboxylate 4,7-dihydro-3-methyl-4-oxo-7-pentylisoxazolo[5,4-b]pyridine-5-carboxylic acid 3-methylisoxazolo[5,4-b]pyridine-4,6-diol