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

4-(3-(3-Methoxybenzyl)-2-oxo-2,3-dihydrooxazolo[5,4-b]pyrazin-5-yl)-N-methyl benzamide | 1021915-86-5

中文名称
——
中文别名
——
英文名称
4-(3-(3-Methoxybenzyl)-2-oxo-2,3-dihydrooxazolo[5,4-b]pyrazin-5-yl)-N-methyl benzamide
英文别名
4-[3-[(3-methoxyphenyl)methyl]-2-oxo-[1,3]oxazolo[4,5-b]pyrazin-5-yl]-N-methylbenzamide
4-(3-(3-Methoxybenzyl)-2-oxo-2,3-dihydrooxazolo[5,4-b]pyrazin-5-yl)-N-methyl benzamide化学式
CAS
1021915-86-5
化学式
C21H18N4O4
mdl
——
分子量
390.398
InChiKey
FULDNHWKUDEHPZ-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):
    2.3
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    93.6
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • Heteroaryl compounds, compositions thereof, and methods of treatment therewith
    申请人:Mortensen Deborah Sue
    公开号:US20090023724A1
    公开(公告)日:2009-01-22
    Provided herein are Heteroaryl Compounds having the following structure: wherein R 1 , R 2 , L, X, Y, Z, Q, A and B are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.
    本文提供具有以下结构的杂环芳基化合物:其中R1,R2,L,X,Y,Z,Q,A和B的定义如下,包括有效量的杂环芳基化合物的组合物以及治疗或预防癌症,炎症状况,免疫状况,代谢状况以及通过抑制激酶通路可治疗或预防的状况的方法,包括向需要治疗的患者中给予有效量的杂环芳基化合物。
  • METHODS OF TREATMENT COMPRISING THE ADMINISTRATION OF HETEROARYL COMPOUNDS
    申请人:Mortensen Deborah Sue
    公开号:US20110245245A1
    公开(公告)日:2011-10-06
    Provided herein are Heteroaryl Compounds having the following structure: wherein R 1 , R 2 , L, X, Y, Z, Q, A and B are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.
    本文提供了具有以下结构的杂环芳基化合物:其中R1、R2、L、X、Y、Z、Q、A和B的定义如下,包括有效量的杂环芳基化合物的组合物,并且治疗或预防癌症、炎症状况、免疫病状况、代谢病状况和通过抑制激酶途径可治疗或预防的病状况的方法包括向需要治疗的患者中施用有效量的杂环芳基化合物。
  • Treatment of cancer with TOR kinase inhibitors
    申请人:Signal Pharmaceuticals, LLC
    公开号:US11166950B2
    公开(公告)日:2021-11-09
    Provided herein are methods for treating or preventing a solid tumor, non-Hodgkin lymphoma or multiple myeloma in a patient, comprising administering an effective amount of a TOR kinase inhibitor to a patient having a solid tumor, non-Hodgkin lymphoma or multiple myeloma.
    本文提供了治疗或预防患者实体瘤、非霍奇金淋巴瘤或多发性骨髓瘤的方法,包括向患有实体瘤、非霍奇金淋巴瘤或多发性骨髓瘤的患者施用有效量的TOR激酶抑制剂。
  • HETEROARYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
    申请人:Signal Pharmaceuticals LLC
    公开号:EP2078016A2
    公开(公告)日:2009-07-15
  • Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors
    申请人:Signal Pharmaceuticals, LLC
    公开号:EP2090577B1
    公开(公告)日:2017-04-05
查看更多

同类化合物

5-羟基-异恶唑[4,5-B]吡嗪-3-甲酸甲酯 5-氯吡嗪并[2,3-d]异�f唑 3-氨基异噁唑并[4,5-b]吡嗪 (1S,2R,19R,22S,34S,37R,40R,52R)-2-{[(2R,3R,4R,5S,6R)-3-(乙酰基氨基)-4,5-二羟基-6-(羟甲基)四氢-2H-吡喃-2-基]氧代}-22-氨基-5,15-二氯-64-({(2S,3R,4R,5S,6R)-4,5-二羟基-6-(羟甲基)-3-[(9-甲基癸酰)氨基]四氢-2H-吡喃-2 3-Methyl-6-nitro-isoxazolo<4,5-b>pyrazin-7-oxid 4-(3-(3-Methoxybenzyl)-2-oxo-2,3-dihydrooxazolo[5,4-b]pyrazin-5-yl)-N-methyl benzamide 5-Chloroisoxazolo[4,5-b]pyrazin-3-amine 5-Methyl-[1,3]oxazolo[4,5-b]pyrazin-2-amine 3-Tert-butyl-[1,2]oxazolo[4,5-b]pyrazine 5-Bromoisoxazolo[4,5-b]pyrazin-3-amine 4-[[3-[(3-Methoxyphenyl)methyl]-2-oxo-[1,3]oxazolo[4,5-b]pyrazin-5-yl]methyl]benzamide 2-([1,3]Oxazolo[4,5-b]pyrazin-5-ylamino)ethanesulfonamide 5,6-Dimethyl-[1,2]oxazolo[4,5-b]pyrazine Butyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Ethyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 5-Fluoro-isoxazolo[4,5-b]pyrazine-3-carboxylic acid methyl ester Hexyl 5-fluoro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Ethyl 5-fluoro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 2-Methylpropyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 2,2-Dimethylpropyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Hexyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 2-Methylpropyl 5-fluoro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 5-chloro-N,N-diethyl-[1,2]oxazolo[4,5-b]pyrazine-3-carboxamide (5-Chloro-[1,2]oxazolo[4,5-b]pyrazin-3-yl)-pyrrolidin-1-ylmethanone Butyl 5-fluoro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Cyclohexyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Propan-2-yl 5-fluoro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Propan-2-yl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate Propyl 5-chloro-[1,2]oxazolo[4,5-b]pyrazine-3-carboxylate 6-Methyl-[1,2]oxazolo[4,5-b]pyrazine 2-Methyl-[1,3]oxazolo[4,5-b]pyrazine 5-Methyl-[1,3]oxazolo[4,5-b]pyrazine 6-Methyl-[1,3]oxazolo[4,5-b]pyrazine 5-Methyl-[1,2]oxazolo[4,5-b]pyrazine 3-Methylisoxazolo<4,5-b>pyridin