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2-[4-(2-fluorophenyl)piperazin-1-yl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one | 1104812-25-0

中文名称
——
中文别名
——
英文名称
2-[4-(2-fluorophenyl)piperazin-1-yl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one
英文别名
2-[4-(2-Fluorophenyl)piperazin-1-yl]-8-nitro-6-(trifluoromethyl)-1,3-benzothiazin-4-one
2-[4-(2-fluorophenyl)piperazin-1-yl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one化学式
CAS
1104812-25-0
化学式
C19H14F4N4O3S
mdl
——
分子量
454.405
InChiKey
IDNXLFOQOLAAPH-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):
    4.2
  • 重原子数:
    31
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    107
  • 氢给体数:
    0
  • 氢受体数:
    9

文献信息

  • New antimicrobial compounds, their synthesis and their use for treatment of mammalian infection
    申请人:Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e.V. Hans-Knöll-Institut
    公开号:EP2020406A1
    公开(公告)日:2009-02-04
    The present invention relates to new antimicrobial compounds, their synthesis and their use for treatment of mammalian infections The present invention aims at the generation of new compounds with activity against mycobacteria as potential new tuberculosis drugs to overcome problems concerning resistance and drug intolerance. This aim has been solved by providing compounds of the formula I wherein R1 and R2 are, independently of each other, NO2, NR7R8, NHOR9, COOR9, CN, CONR10R11, CHO, F, Cl, Br, SO2NR12R13, lower alkoxy, OCF3, mono-, di or trifluoromethyl; R3 and R4 are, independently of each other, H, a saturated or unsaturated, linear or branched aliphatic radical having 1-3 chain members, F, Cl, Br, lower alkoxy; R5 is H, a saturated or unsaturated, halogenated or unhalogenated, linear or branched aliphatic radical having 1-7 chain members; R6 is a radical: wherein X is saturated or unsaturated, halogenated or unhalogenated, linear or branched aliphatic radical having 1-5 chain members, or R5 and R6 together represent bivalent radicals wherein n is 1-4: R7 - R13 are, independently of each other H or a saturated or unsaturated, halogenated or unhalogenated, linear or branched aliphatic radical having 1-5 chain members, phenyl, benzyl or R7 and R8 together, R10 and R11 together, R12 and R13 together represent a linear or branched aliphatic bivalent radical having 1-7 chain members; R14 and R15 are, independently of each other, H, linear or branched aliphatic radical having 1-5 chain members, F, Cl, Br, NO2, NH2, CF3.
    本发明涉及新的抗菌化合物,它们的合成以及它们用于治疗哺乳动物感染的用途。本发明旨在生成具有对抗结核分枝杆菌活性的新化合物,作为潜在的新结核病药物,以克服有关耐药性和药物不耐受性的问题。这一目标已通过提供具有以下结构的化合物来实现:其中R1和R2独立于彼此,为NO2、NR7R8、NHOR9、COOR9、CN、CONR10R11、CHO、F、Cl、Br、SO2NR12R13、低碳醇基、O 、单、二或三甲基;R3和R4独立于彼此,为H、具有1-3个链成员的饱和或不饱和、线性或支链脂肪基、F、Cl、Br、低碳醇基;R5为H、具有1-7个链成员的饱和或不饱和、卤代或非卤代、线性或支链脂肪基;R6为一个基团:其中X为具有1-5个链成员的饱和或不饱和、卤代或非卤代、线性或支链脂肪基,或R5和R6一起代表n为1-4的二价基团;R7-R13独立于彼此,为H或具有1-5个链成员的饱和或不饱和、卤代或非卤代、线性或支链脂肪基、苯基、苄基或R7和R8一起、R10和R11一起、R12和R13一起代表具有1-7个链成员的线性或支链脂肪双价基团;R14和R15独立于彼此,为H、具有1-5个链成员的线性或支链脂肪基、F、Cl、Br、 、NH2、CF3
  • ANTIMICROBIAL COMPOUNDS, THEIR SYNTHESIS AND THEIR USE FOR TREATMENT OF MAMMALIAN INFECTIONS
    申请人:Moellmann Ute
    公开号:US20100286130A1
    公开(公告)日:2010-11-11
    The present invention relates to compounds of Formula (I) or salts thereof wherein R′, R 2 , R 3 , R 4 , R 5 , R 6 , and other variables enumerated under one or more of same are as defined herein. Compounds of Formula I have activity as antimicrobial agents. Also disclosed are pharmaceutical compositions and methods of treating and preventing microbial infections in mammals, for example, a tuberculosis or leprosy infection, which employ compounds of Formula (I) or salts thereof.
    本发明涉及式(I)化合物或其盐,其中R′,R2,R3,R4,R5,R6和在同一或多个中列举的其他变量如下所定义。式(I)化合物具有抗微生物活性。本发明还公开了使用式(I)化合物或其盐治疗和预防哺乳动物中的微生物感染的制药组合物和方法,例如结核病或麻风感染。
  • Low-swelling biocompatible hydrogels
    申请人:Confluent Surgical Inc.
    公开号:EP1967220A2
    公开(公告)日:2008-09-10
    Some aspects of the present disclosure relate to a surgical treatment for treating a tissue inside a vertebral column by forming a low-swelling biodegradable hydrogel in situ adherent to a tissue inside the vertebral column and substantially exterior to a theca in the vertebral column.
    本公开的某些方面涉及一种用于治疗椎体内组织的手术疗法,其方法是在原位形成一种低膨胀可生物降解凝胶,粘附在椎体内的组织上,并且基本上位于椎体内的椎孔外。
  • Extra luminal scaffold
    申请人:Incept, LLC
    公开号:US10550187B2
    公开(公告)日:2020-02-04
    Methods and devices for treating a luminal pathology affecting an anatomical lumen of a patient comprising forming, in situ, a continuous cohesive layer of covalently-crosslinked hydrogel in a luminal wall of the anatomical lumen.
    用于治疗影响患者解剖管腔的管腔病变的方法和设备,包括在解剖管腔的管壁中就地形成共价交联凝胶的连续内聚层。
  • NEW ANTIMICROBIAL COMPOUNDS, THEIR SYNTHESIS AND THEIR USE FOR TREATMENT OF MAMMALIAN INFECTIONS
    申请人:Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e.V. Hans-Knöll-Institut
    公开号:EP2176248B1
    公开(公告)日:2010-09-29
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