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4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, magnesium salt (2:1), [2S-(2alpha,5alpha,6beta)]- | 40182-54-5

中文名称
——
中文别名
——
英文名称
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, magnesium salt (2:1), [2S-(2alpha,5alpha,6beta)]-
英文别名
——
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, magnesium salt (2:1), [2S-(2alpha,5alpha,6beta)]-化学式
CAS
40182-54-5
化学式
C19H17ClFMgN3O5S
mdl
——
分子量
478.2
InChiKey
XNXJNOBKIQGNET-SLINCCQESA-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):
    2.31
  • 重原子数:
    31
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    138
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • GAMMA-AAPEPTIDES WITH POTENT AND BROAD-SPECTRUM ANTIMICROBIAL ACTIVITY
    申请人:Cai Jianfeng
    公开号:US20150274782A1
    公开(公告)日:2015-10-01
    The present invention is directed to a novel class of antimicrobial agents called γ-AApeptides. The current invention provides various categories of γ-AApeptides, for example, linear γ-AApeptides, cyclic γ-AApeptides, and lipidated γ-AApeptides. γ-AApeptides of the current invention are designed to exert antimicrobial activity while being stable and non-toxic. γ-AApeptides also do not appear to lead to the development of microbial resistance in treated microorganisms. Thus, the disclosed γ-AApeptides can be used for the treatment of various medical conditions associated with pathogenic microorganisms.
    本发明涉及一种新型类别的抗微生物药物,称为γ-AA肽。当前发明提供了各种类别的γ-AA肽,例如线性γ-AA肽、环状γ-AA肽和脂质化γ-AA肽。本发明的γ-AA肽被设计为具有抗微生物活性,同时稳定且无毒。γ-AA肽似乎也不会导致被治疗微生物体内微生物产生抗药性。因此,所披露的γ-AA肽可用于治疗与病原微生物相关的各种医疗状况。
  • An otorhinological drug delivery device
    申请人:Schering Oy
    公开号:EP1438942A1
    公开(公告)日:2004-07-21
    The invention relates to an otorhinological delivery device comprising at least one pharmaceutically active agent. According to the invention the device comprises a core comprising said at least one pharmaceutically active agent wherein said core is made of an elastomer composition selected from the group consisting of poly(dimethylsiloxane), a siloxane-based elastomer comprising 3,3,3-trifluoropropyl groups attached to the Si-atoms of the siloxane units, a siloxane-based elastomer comprising poly(alkylene oxide) groups and mixtures thereof.
    本发明涉及一种包含至少一种药用活性剂的耳鼻喉给药装置。根据本发明,该装置包括一个包含所述至少一种药物活性剂的芯体,其中所述芯体由弹性体组合物制成,该弹性体组合物选自聚(二甲基硅氧烷)、硅氧烷基弹性体(包含连接到硅氧烷单元S原子上的3,3,3-三氟丙基)、硅氧烷基弹性体(包含聚(环氧烷)基团)及其混合物组成的组。
  • γ-AApeptides with potent and broad-spectrum antimicrobial activity
    申请人:Cai Jianfeng
    公开号:US10144764B2
    公开(公告)日:2018-12-04
    The present invention is directed to a novel class of antimicrobial agents called γ-AApeptides. The current invention provides various categories of γ-AApeptides, for example, linear γ-AApeptides, cyclic γ-AApeptides, and lipidated γ-AApeptides. γ-AApeptides of the current invention are designed to exert antimicrobial activity while being stable and non-toxic. γ-AApeptides also do not appear to lead to the development of microbial resistance in treated microorganisms. Thus, the disclosed γ-AApeptides can be used for the treatment of various medical conditions associated with pathogenic microorganisms.
    本发明涉及一类名为γ-AA肽的新型抗菌剂。本发明提供了各种类型的 γ-AA肽,例如线性γ-AA肽、环状γ-AA肽和脂化γ-AA肽。本发明中的γ-AA 肽具有抗菌活性,同时稳定无毒。γ-AA肽似乎也不会导致被处理微生物产生抗药性。因此,所公开的γ-AA 肽可用于治疗与病原微生物有关的各种病症。
  • Gamma-AApeptides with potent and broad-spectrum antimicrobial activity
    申请人:Cai Jianfeng
    公开号:US10308686B2
    公开(公告)日:2019-06-04
    The present invention is directed to a novel class of antimicrobial agents called γ-AApeptides. The current invention provides various categories of γ-AApeptides, for example, linear γ-AApeptides, cyclic γ-AApeptides, and lipidated γ-AApeptides. γ-AApeptides of the current invention are designed to exert antimicrobial activity while being stable and non-toxic. γ-AApeptides also do not appear to lead to the development of microbial resistance in treated microorganisms. Thus, the disclosed γ-AApeptides can be used for the treatment of various medical conditions associated with pathogenic microorganisms.
    本发明涉及一类名为γ-AA肽的新型抗菌剂。本发明提供了各种类型的 γ-AA肽,例如线性γ-AA肽、环状γ-AA肽和脂化γ-AA肽。本发明中的γ-AA 肽具有抗菌活性,同时稳定无毒。γ-AA肽似乎也不会导致被处理微生物产生抗药性。因此,所公开的γ-AA 肽可用于治疗与病原微生物有关的各种病症。
  • Sustained-release injectable formulation
    申请人:Friedman Michael
    公开号:US11052043B2
    公开(公告)日:2021-07-06
    A composition which comprises a biologically active agent and a polymer that exhibits a reverse thermal gelation at a physiological temperature, in a carrier, and in which the active agent is in an undissolved form is disclosed herein. Further disclosed herein are methods utilizing the compositions for treating subjects, including non-human subjects, as well as kits for preparing and using a composition. The composition is preferably a sustained release formulation, and is particularly useful for treating animals, where single-dose treatment is desired.
    本文公开了一种组合物,该组合物由生物活性剂和在生理温度下呈现反向热凝胶化的聚合物组成,其载体中的活性剂为未溶解形式。本文进一步公开了利用组合物治疗受试者(包括非人类受试者)的方法,以及制备和使用组合物的试剂盒。组合物最好是缓释制剂,尤其适用于治疗动物,因为动物需要单剂量治疗。
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