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{5-[1-(4-aminobutyl)imidazol-4-yl]-(2-pyridyl)}dimethylamine | 790262-74-7

中文名称
——
中文别名
——
英文名称
{5-[1-(4-aminobutyl)imidazol-4-yl]-(2-pyridyl)}dimethylamine
英文别名
{5-[1-(4-aminobutyl)imidazol-4-yl](2-pyridil)}dimethylamine;5-[1-(4-aminobutyl)imidazol-4-yl]-N,N-dimethylpyridin-2-amine
{5-[1-(4-aminobutyl)imidazol-4-yl]-(2-pyridyl)}dimethylamine化学式
CAS
790262-74-7
化学式
C14H21N5
mdl
——
分子量
259.354
InChiKey
UFDZCQISEHSRBP-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

物化性质

  • 沸点:
    495.1±45.0 °C(Predicted)
  • 密度:
    1.14±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    19
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    60
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    {5-[1-(4-aminobutyl)imidazol-4-yl]-(2-pyridyl)}dimethylamine甲醇 作用下, 以 乙腈 为溶剂, 反应 28.0h, 生成 (1S,2R,5R,7R,8R,9R,11R,13R,14R)-8-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-15-[4-[4-[6-(dimethylamino)pyridin-3-yl]imidazol-1-yl]butyl]-1-ethenyl-2-ethyl-9-methoxy-5,7,9,11,13-pentamethyl-3,17-dioxa-15-azabicyclo[12.3.0]heptadecane-4,6,12,16-tetrone
    参考文献:
    名称:
    Synthesis and Antibacterial Activity of Novel C12 Vinyl Ketolides
    摘要:
    A novel series Of C-12 vinyl erythromycin derivatives have been discovered which exhibit in vitro and in vivo potency against key respiratory pathogens. The C-12 modification involves replacing the natural C-12 methyl group in the erythromycin core with a vinyl group via chemical synthesis. From the C-12 vinyl macrolide core, a series Of C-12 vinyl ketolides was prepared. Several compounds were found to be potent against macrolide-sensitive and -resistant bacteria. The C-12 vinyl ketolides 6j and 6k showed a similar antimicrobial spectrum and comparable activity to the commercial ketolide telithromycin. However, the pharmacokinetic profiles Of C-12 vinyl ketolides 6j and 6k in rats differ from that of telithromycin by having higher lung-to-plasma ratios, larger volumes of distribution, and longer half-lives. These pharmacokinetic differences have a pharmacodynamic effect as both 6j and 6k exhibited better in vivo efficacy than telithromycin in rat lung infection models against Streptococcus pneumoniae and Haemophilus influenzae.
    DOI:
    10.1021/jm051157a
  • 作为产物:
    参考文献:
    名称:
    Synthesis and Antibacterial Activity of Novel C12 Vinyl Ketolides
    摘要:
    A novel series Of C-12 vinyl erythromycin derivatives have been discovered which exhibit in vitro and in vivo potency against key respiratory pathogens. The C-12 modification involves replacing the natural C-12 methyl group in the erythromycin core with a vinyl group via chemical synthesis. From the C-12 vinyl macrolide core, a series Of C-12 vinyl ketolides was prepared. Several compounds were found to be potent against macrolide-sensitive and -resistant bacteria. The C-12 vinyl ketolides 6j and 6k showed a similar antimicrobial spectrum and comparable activity to the commercial ketolide telithromycin. However, the pharmacokinetic profiles Of C-12 vinyl ketolides 6j and 6k in rats differ from that of telithromycin by having higher lung-to-plasma ratios, larger volumes of distribution, and longer half-lives. These pharmacokinetic differences have a pharmacodynamic effect as both 6j and 6k exhibited better in vivo efficacy than telithromycin in rat lung infection models against Streptococcus pneumoniae and Haemophilus influenzae.
    DOI:
    10.1021/jm051157a
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文献信息

  • Novel ketolide derivatives
    申请人:Burger Matthew
    公开号:US20050153905A1
    公开(公告)日:2005-07-14
    Antimicrobial ketolide compounds are provided having the formula (A): as well as pharmaceutically acceptable salts, esters or prodrugs thereof, pharmaceutical compositions comprising such compounds, methods of treating bacterial infections by the administration of such compounds, and processes for the preparation of the compounds.
    提供具有以下公式(A)的抗微生物酮类化合物,以及其药学上可接受的盐、酯或前药,包含这种化合物的药物组合物,通过给予这种化合物的途径治疗细菌感染的方法,以及制备这种化合物的方法。
  • Pyridyl substituted ketolide antibiotics
    申请人:Burger T. Matthew
    公开号:US20050009764A1
    公开(公告)日:2005-01-13
    Antimicrobial macrolide and ketolide compounds are provided having formulas XII: as well as pharmaceutically acceptable salts, esters or prodrugs thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of the compounds.
    提供具有XII式的抗微生物大环内酯和酮内酯化合物,以及其药学上可接受的盐、酯或前药;包含这些化合物的药物组合物;通过给予这些化合物的途径治疗细菌感染的方法;以及制备这些化合物的过程。
  • [EN] PYRIDYL SUBSTITUTED KETOLIDE ANTIBIOTICS<br/>[FR] ANTIBIOTIQUES A BASE DE KETOLIDE A SUBSTITUTION PYRIDYLE
    申请人:CHIRON CORP
    公开号:WO2004096822A3
    公开(公告)日:2004-12-16
  • [EN] NOVEL KETOLIDE DERIVATIVES<br/>[FR] NOUVEAUX DERIVES DE KETOLIDES
    申请人:CHIRON CORP
    公开号:WO2004096823A3
    公开(公告)日:2005-02-10
  • US7163924B2
    申请人:——
    公开号:US7163924B2
    公开(公告)日:2007-01-16
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