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(R)-(3-(3-fluoro-4-(6-(methyl(1-methyl-1H-tetrazol-5-yl)amino) pyridin-3-yl)phenyl)oxazolidin-2-one-5-yl)methyl dihydrogen phosphate | 1428960-82-0

中文名称
——
中文别名
——
英文名称
(R)-(3-(3-fluoro-4-(6-(methyl(1-methyl-1H-tetrazol-5-yl)amino) pyridin-3-yl)phenyl)oxazolidin-2-one-5-yl)methyl dihydrogen phosphate
英文别名
[(5R)-3-[3-fluoro-4-[6-[methyl-(1-methyltetrazol-5-yl)amino]pyridin-3-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl dihydrogen phosphate
(R)-(3-(3-fluoro-4-(6-(methyl(1-methyl-1H-tetrazol-5-yl)amino) pyridin-3-yl)phenyl)oxazolidin-2-one-5-yl)methyl dihydrogen phosphate化学式
CAS
1428960-82-0
化学式
C18H19FN7O6P
mdl
——
分子量
479.364
InChiKey
YXHSGBSYMPDWCW-CYBMUJFWSA-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:
    33
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    156
  • 氢给体数:
    2
  • 氢受体数:
    12

文献信息

  • BIARYL HETEROCYCLE SUBSTITUTED OXAZOLIDINONE ANTIBACTERIAL AGENTS
    申请人:Xuanzhu Pharma Co., Ltd.
    公开号:US20140235584A1
    公开(公告)日:2014-08-21
    The present invention relates to a biaryl heterocycle substituted oxazolidinone antibacterials shown by general formula (I), a pharmaceutically acceptable salt thereof, an isomer or a prodrug thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , A and B are as defined in the description. The present invention further relates to a method for preparing the compound, a pharmaceutical composition and a pharmaceutical formulation comprising the compound, and a use of the compound in the manufacture of a medicament for the treatment and/or prevention of infectious diseases and a use for the treatment and/or prevention of infectious diseases.
    本发明涉及一种由一般式(I)所示的取代的双芳基杂环氧唑啉酮抗菌剂,其药学上可接受的盐,其异构体或其前药,其中R1、R2、R3、R4、R5、A和B如描述中所定义。本发明还涉及一种制备该化合物的方法,包括该化合物的药物组合物和药物配方,以及该化合物在制造用于治疗和/或预防传染病的药物和用于治疗和/或预防传染病的用途。
  • (METH)ACRYLOYL-TERMINATED POLYISOBUTYLENE POLYMER, METHOD FOR PRODUCING THE SAME, AND ACTIVE ENERGY RAY-CURABLE COMPOSITION
    申请人:KANEKA CORPORATION
    公开号:US20140243444A1
    公开(公告)日:2014-08-28
    The purpose of the present invention is to provide a polymer having a low halogen atom content remaining in the polymer, a simple production method thereof, an active energy ray-curable composition that can be rapidly cured by an irradiation of a small amount of light, and a cured product thereof. These purpose can be achieved by an active energy ray-curable composition, including a polyisobutylene polymer (A) represented by the following general formula (1) (wherein R 1 represents a monovalent or polyvalent aromatic hydrocarbon group, or a monovalent or a polyvalent aliphatic hydrocarbon group; A represents a polyisobutylene polymer; R 2 represents a divalent saturated hydrocarbon group having 2-6 carbon atoms, which contains no hetero atoms; R 3 and R 4 each represent hydrogen, a monovalent hydrocarbon group having 1-20 carbon atoms, or an alkoxy group having 1-20 carbon atoms; R 5 represents hydrogen or a methyl group; and n denotes a natural number), and an active energy ray polymerization initiator (B).
    本发明的目的是提供一种聚合物,其聚合物中保留有较低的卤素原子含量,以及其简单的生产方法,一种能够通过少量光辐照快速固化的活性能量射线固化组合物以及其固化产物。这些目的可以通过一种活性能量射线固化组合物来实现,包括以下通式(1)所表示的聚异丁烯聚合物(A)(其中R1表示单价或多价芳香烃基或单价或多价脂肪烃基;A表示聚异丁烯聚合物;R2表示含有2-6个碳原子的二价饱和碳氢基团,不含杂原子;R3和R4分别表示氢、具有1-20个碳原子的单价碳氢基团或具有1-20个碳原子的烷氧基;R5表示氢或甲基基团;n表示自然数),以及活性能量射线聚合引发剂(B)。
  • BIARYL HETEROCYCLE SUBSTITUTED OXAZOLIDINON ANTIBACTERIAL DRUG
    申请人:Xuanzhu Pharma Co., Ltd.
    公开号:EP2762479A1
    公开(公告)日:2014-08-06
    The present invention relates to a biaryl heterocycle substituted oxazolidinone antibacterials shown by general formula (I), a pharmaceutically acceptable salt thereof, an isomer or a prodrug thereof, wherein R1, R2, R3, R4, R5, A and B are as defined in the description. The present invention further relates to a method for preparing the compound, a pharmaceutical composition and a pharmaceutical formulation comprising the compound, and a use of the compound in the manufacture of a medicament for the treatment and/or prevention of infectious diseases and a use for the treatment and/or prevention of infectious diseases.
    本发明涉及通式(I)所示的双芳基杂环取代的噁唑酮类抗菌剂、其药学上可接受的盐、异构体或原药,其中R1、R2、R3、R4、R5、A和B如描述中所定义。本发明进一步涉及制备该化合物的方法、包含该化合物的药物组合物和药物制剂,以及该化合物在制造治疗和/或预防传染性疾病的药物中的用途和治疗和/或预防传染性疾病的用途。
  • (METH)ACRYLOYL-TERMINATED POLYISOBUTYLENE POLYMER, METHOD FOR PRODUCING SAME, AND ACTIVE ENERGY RAY-CURABLE COMPOSITION
    申请人:Kaneka Corporation
    公开号:EP2762506A1
    公开(公告)日:2014-08-06
    The purpose of the present invention is to provide a polymer having a low halogen atom content remaining in the polymer, a simple production method thereof, an active energy ray-curable composition that can be rapidly cured by an irradiation of a small amount of light, and a cured product thereof. These purpose can be achieved by an active energy ray-curable composition, including a polyisobutylene polymer (A) represented by the following general formula (1) (wherein R1 represents a monovalent or polyvalent aromatic hydrocarbon group, or a monovalent or a polyvalent aliphatic hydrocarbon group; A represents a polyisobutylene polymer; R2 represents a divalent saturated hydrocarbon group having 2-6 carbon atoms, which contains no hetero atoms; R3 and R4 each represent hydrogen, a monovalent hydrocarbon group having 1-20 carbon atoms, or an alkoxy group having 1-20 carbon atoms; R5 represents hydrogen or a methyl group; and n denotes a natural number), and an active energy ray polymerization initiator (B).
    本发明的目的是提供一种在聚合物中残留卤原子含量低的聚合物、一种简单的生产方法、一种可通过少量光照射快速固化的活性能量射线固化组合物及其固化产品。这些目的可以通过一种活性能量射线固化组合物来实现,该组合物包括由以下通式(1)表示的聚异丁烯聚合物(A)(其中 R1 代表一价或多价芳香烃基团,或一价或多价脂肪烃基团;A 代表聚异丁烯聚合物;R2 代表具有 2-6 个碳原子、不含杂原子的二价饱和烃基;R3 和 R4 分别代表氢、具有 1-20 个碳原子的一价烃基或具有 1-20 个碳原子的烷氧基;R5 代表氢或甲基;n 表示自然数),以及活性能量射线聚合引发剂 (B)。
  • [EN] BIARYL HETEROCYCLE SUBSTITUTED OXAZOLIDINON ANTIBACTERIAL DRUG<br/>[FR] MÉDICAMENT ANTIBACTÉRIEN À BASE D'OXAZOLIDINONE SUBSTITUÉE PAR UN HÉTÉROCYCLE BIARYLIQUE
    申请人:XUANZHU PHARMA CO LTD
    公开号:WO2013044845A1
    公开(公告)日:2013-04-04
    本发明涉及通式(I)所示的联芳基杂环取代的噁唑烷酮抗菌药化合物、其药学上可接受的盐、异构体或其前药,其中R1、R2、R3、R4、R5、A和B的定义同说明书中所述定义;本发明还涉及这些化合物的制备方法,含有这些化合物的药物组合物和药物制剂,以及这些化合物在制备治疗和/或预防感染性疾病的药物和治疗和/或预防感染性疾病方面的应用。
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