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8-chloro-6,7-dihydroxy-3-methyl-2H-phthalazine-1,4-dione

中文名称
——
中文别名
——
英文名称
8-chloro-6,7-dihydroxy-3-methyl-2H-phthalazine-1,4-dione
英文别名
——
8-chloro-6,7-dihydroxy-3-methyl-2H-phthalazine-1,4-dione化学式
CAS
——
化学式
C9H7ClN2O4
mdl
——
分子量
242.61
InChiKey
BALPSJAMQVGZIE-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):
    0.5
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    89.9
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • [EN] 2 SUBSTITUTED CEPHEM COMPOUNDS<br/>[FR] COMPOSÉS DE CÉPHEM SUBSTITUÉS EN POSITION 2
    申请人:GLAXO GROUP LTD
    公开号:WO2014068388A1
    公开(公告)日:2014-05-08
    The compounds of formula (I) of the subject invention are related to 2-substituted cephem compounds, which have a wide antimicrobial spectrum, in particular exhibit potent antimicrobial activity against beta-lactamase producing Gram negative bacteria, and pharmaceutical compositions comprising the same.
    本发明的化学式(I)的化合物与2-取代头孢菌素类化合物相关,具有广泛的抗微生物谱,特别对产β-内酰胺酶的革兰氏阴性细菌表现出强效的抗微生物活性,并且包含这些化合物的药物组合物。
  • CEPHEM COMPOUND
    申请人:SHIONOGI & CO., LTD.
    公开号:US20150344502A1
    公开(公告)日:2015-12-03
    A compound of the formula: wherein, W is —CH2 − etc.; U is —S − etc.; R 1 is substituted or unsubstituted carbocyclyl etc.; R 2A and R 2B is a) or b) described in the specification; R 3 is a hydrogen atom etc.; R 11 is carboxylate anion (—COO − ) etc.; L is substituted or unsubstituted lower alkylene etc., E is a substituted or unsubstituted divalent group containing quaternary ammonium ion; G is a single bond etc.; D is —C(═O)—C(═O)—NR 6 — etc.; R 10 1) to 3) described in specification; or an amino-protected compound when the amino group is present on the ring in the 7-side chain, or a pharmaceutically acceptable salt thereof.
    公式为:其中,W为—CH2−等;U为—S−等;R1为取代或未取代的碳环等;R2A和R2B为规范中描述的a)或b);R3为氢原子等;R11为羧酸根离子(—COO−)等;L为取代或未取代的较低烷基等;E为含季铵离子的取代或未取代的双价基团;G为单键等;D为—C(═O)—C(═O)—NR6—等;R10为规范中描述的1)至3);或者是7-侧链环上存在氨基时的氨基保护化合物,或其药用可接受盐。
  • 2-SUBSTITUTED CEPHEM COMPOUNDS
    申请人:GLAXO GROUP LIMITED
    公开号:US20150299223A1
    公开(公告)日:2015-10-22
    The present invention relates to 2-substituted cephem compounds of Formula (I) having a quaternary ammonium group on the 3-side chain, preferably together with a cathechol group, or pharmaceutically acceptable salts thereof, which exhibit potent antimicrobial spectrum against a variety of bacteria including Gram negative bacteria and/or Gram positive bacteria, corresponding pharmaceutical compositions, methods of making, treatment methods for bacterial infections or uses thereof.
    本发明涉及具有第3侧链上季铵基团的2-取代头孢菌素化合物(I), 与儿茶酚基团一起更佳,或其药学上可接受的盐,对包括革兰氏阴性菌和/或革兰氏阳性菌在内的多种细菌具有强效的抗微生物谱,相应的制药组合物,制备方法,治疗细菌感染的方法或其用途。
  • 2 SUBSTITUTED CEPHEM COMPOUNDS
    申请人:Glaxo Group Limited
    公开号:US20170281532A1
    公开(公告)日:2017-10-05
    The compounds of the subject invention are related to 2-substituted cephem compounds, which have a wide antimicrobial spectrum, in particular exhibit potent antimicrobial activity against beta-lactamase producing Gram negative bacteria, and pharmaceutical compositions comprising the same.
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