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6-Methyl-[1,2]oxazolo[4,5-b]pyrazine

中文名称
——
中文别名
——
英文名称
6-Methyl-[1,2]oxazolo[4,5-b]pyrazine
英文别名
6-methyl-[1,2]oxazolo[4,5-b]pyrazine
6-Methyl-[1,2]oxazolo[4,5-b]pyrazine化学式
CAS
——
化学式
C6H5N3O
mdl
——
分子量
135.12
InChiKey
SMVLOAOYEGBFRS-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):
    0.4
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • SILICON BASED DRUG CONJUGATES AND METHODS OF USING SAME
    申请人:BlinkBio, Inc.
    公开号:US20170202970A1
    公开(公告)日:2017-07-20
    Described herein are silicon based conjugates capable of delivering one or more payload moieties to a target cell or tissue. Contemplated conjugates may include a silicon-heteroatom core, one or more optional catalytic moieties, a targeting moiety that permits accumulation of the conjugate within a target cell or tissue, one or more payload moieties (e.g., a therapeutic agent or imaging agent), and two or more non-interfering moieties covalently bound to the silicon-heteroatom core.
    本文描述了基于硅的共轭物,能够将一个或多个有效载荷基团传递到靶细胞或组织。考虑到的共轭物可能包括一个硅-杂原子核心,一个或多个可选的催化基团,一个定位基团,允许共轭物在靶细胞或组织内积累,一个或多个有效载荷基团(例如,治疗剂或成像剂),以及与硅-杂原子核心共价结合的两个或更多个不干扰基团。
  • [DE] DERIVATE VON 2-BENZYLSULFANYL[1,3,4]-OXADIAZOL UND DEREN MEDIZINISCHE VERWENDUNG<br/>[EN] 2-BENZYLSULFANYL[1,3,4]-OXADIAZOLE DERIVATIVES, AND MEDICAL USE THEREOF<br/>[FR] DÉRIVÉS DE 2-BENZYLSULFANYL[1,3,4]OXADIAZOLE ET UTILISATION DESDITS DÉRIVÉS EN MÉDECINE
    申请人:UNIV DARMSTADT TECH
    公开号:WO2013007663A1
    公开(公告)日:2013-01-17
    Die vorliegende Erfindung betrifft Verbindungen, die als selektive Liganden der Glykogen Synthase Kinase 3 (GSK-3) wirken und für die Behandlung von GSK-3-vermittelten Erkrankungen verwendet werden können. Die erfindungsgemäßen Verbindungen wirken als Inhibitoren der Glykogen Synthase Kinase 3 (GSK-3).
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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