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4-(methylcarbamoyl)-1H-imidazole-5-carboxylic acid | 627470-17-1

中文名称
——
中文别名
——
英文名称
4-(methylcarbamoyl)-1H-imidazole-5-carboxylic acid
英文别名
——
4-(methylcarbamoyl)-1H-imidazole-5-carboxylic acid化学式
CAS
627470-17-1
化学式
C6H7N3O3
mdl
MFCD04474838
分子量
169.14
InChiKey
UQGPYFRGVFBRKT-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:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    95.1
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • CEPHEM COMPOUND HAVING PYRIDINIUM GROUP
    申请人:Nishitani Yasuhiro
    公开号:US20140114060A1
    公开(公告)日:2014-04-24
    The present invention provides a novel compound which has a broad antibacterial spectrum and particularly exhibits a high antibacterial activity on β-lactamase-producing gram-negative bacteria. Specifically provided are: a compound represented by formula (I) wherein the meaning of each symbol is as defined in the description, an amino-group-protected form of a type of the compound which has the amino group on a ring in a position-7 side chain, or a pharmaceutically acceptable salt of the compound or the amino-group-protected form; and a pharmaceutical composition containing the compound, the amino-group-protected form or the pharmaceutically acceptable salt.
    本发明提供了一种新型化合物,具有广泛的抗菌谱,特别对产β-内酰胺酶的革兰氏阴性细菌表现出高抗菌活性。具体提供的是:一种由式(I)表示的化合物,其中每个符号的含义如描述中定义的那样,一种在环上具有氨基团的化合物的保护形式,该化合物在位置-7侧链上具有氨基团,或者化合物或氨基团保护形式的药用可接受盐;以及含有该化合物、氨基团保护形式或药用可接受盐的药物组合物。
  • 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。
  • NOVEL CEPHEM COMPOUND HAVING CATECHOL OR PSEUDO-CATECHOL STRUCTURE
    申请人:Nishitani Yasuhiro
    公开号:US20140088302A1
    公开(公告)日:2014-03-27
    The present invention provides a novel compound which has a wide antimicrobial spectrum, and in particular exhibits potent antimicrobial activity against beta-lactamase producing Gram negative bacteria. Specifically, the present invention provides a compound of the formula (I): wherein each symbol is as defined in the 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, and a pharmaceutical composition comprising the same.
  • PROCESSES FOR PRODUCTION OF INTERMEDIATES FOR 2-ALKYL CEPHEM COMPOUNDS
    申请人:SHIONOGI & CO., LTD.
    公开号:US20150291619A1
    公开(公告)日:2015-10-15
    The invention relates to processes for the production of intermediates for preparing 2-alkyl cephem compounds useful as antimicrobial drugs. The invention provides a process which comprises oxidating a compound of the formula (I) or a salt thereof to give a compound of the formula (II) or a salt thereof wherein each symbol is as defined in the specification.
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