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(2S,3S,4R)-2-methyl-2-([1,3]dioxolan-2-yl)-6-nitro-3-hydroxy-4-amino-3,4-dihydro-2H-1-benzopyran | 335382-28-0

中文名称
——
中文别名
——
英文名称
(2S,3S,4R)-2-methyl-2-([1,3]dioxolan-2-yl)-6-nitro-3-hydroxy-4-amino-3,4-dihydro-2H-1-benzopyran
英文别名
(2S,3S,4R)-4-amino-2-(1,3-dioxolan-2-yl)-2-methyl-6-nitro-3,4-dihydrochromen-3-ol
(2S,3S,4R)-2-methyl-2-([1,3]dioxolan-2-yl)-6-nitro-3-hydroxy-4-amino-3,4-dihydro-2H-1-benzopyran化学式
CAS
335382-28-0
化学式
C13H16N2O6
mdl
——
分子量
296.28
InChiKey
KALTYCRCEBCFIT-MDZLAQPJSA-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):
    -0.3
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    120
  • 氢给体数:
    2
  • 氢受体数:
    7

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:
    (2S,3S,4R)-2-methyl-2-([1,3]dioxolan-2-yl)-6-nitro-3-hydroxy-4-amino-3,4-dihydro-2H-1-benzopyran 在 sodium tetrahydroborate 、 copper diacetate 、 三乙胺 作用下, 以 甲醇N,N-二甲基甲酰胺异丙醇 为溶剂, 反应 1.0h, 生成 (2S,3S,4R)-N-[6-amino-3,4-dihydro-2-([1,3]dioxolan-2-yl)-3-hydroxy-2-methyl-2H-benzopyran-4-yl]-N'-benzyl-N''-cyanoguanidine
    参考文献:
    名称:
    A Novel Anti-Ischemic ATP-Sensitive Potassium Channel (KATP) Opener without Vasorelaxation:  N-(6-Aminobenzopyranyl)-N‘-benzyl-N‘ ‘-cyanoguanidine Analogue
    摘要:
    This paper describes the design, synthesis, and biological evaluation of a novel anti-ischemic compound, (2S,3S,4R)-N-(6-amino-3,4-dihydro-2-dimethoxymethyl-3-hydroxy-2-methyl-2H-benzopyranyl)-N'-benzyl-N " -cyanoguanidine (33), and the structure-activity relationships leading to the discovery of this compound. Compound 33 significantly reduced the myocardial infarct zone to area at risk (IZ/AAR) in the ischemic myocardium rat model with high cardioselectivity. Since the cardioprotective effect of compound 33 is reversed by ATP-sensitive potassium channel (K-ATP) blockers, its anti-ischemic effect appears to be at least mediated by K-ATP opening. In addition, compound 33 shows good protective activity on neuronal cells against oxidative stress, and therefore it is suggested that compound 33 may have therapeutic potential both in cardio- and in neuroprotection.
    DOI:
    10.1021/jm010183f
  • 作为产物:
    参考文献:
    名称:
    A Novel Anti-Ischemic ATP-Sensitive Potassium Channel (KATP) Opener without Vasorelaxation:  N-(6-Aminobenzopyranyl)-N‘-benzyl-N‘ ‘-cyanoguanidine Analogue
    摘要:
    This paper describes the design, synthesis, and biological evaluation of a novel anti-ischemic compound, (2S,3S,4R)-N-(6-amino-3,4-dihydro-2-dimethoxymethyl-3-hydroxy-2-methyl-2H-benzopyranyl)-N'-benzyl-N " -cyanoguanidine (33), and the structure-activity relationships leading to the discovery of this compound. Compound 33 significantly reduced the myocardial infarct zone to area at risk (IZ/AAR) in the ischemic myocardium rat model with high cardioselectivity. Since the cardioprotective effect of compound 33 is reversed by ATP-sensitive potassium channel (K-ATP) blockers, its anti-ischemic effect appears to be at least mediated by K-ATP opening. In addition, compound 33 shows good protective activity on neuronal cells against oxidative stress, and therefore it is suggested that compound 33 may have therapeutic potential both in cardio- and in neuroprotection.
    DOI:
    10.1021/jm010183f
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文献信息

  • BENZOPYRANYL GUANIDINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:Dongbu Hannong Chemical Co., Ltd.
    公开号:EP1228058B1
    公开(公告)日:2003-12-10
  • US6323238B1
    申请人:——
    公开号:US6323238B1
    公开(公告)日:2001-11-27
  • A Novel Anti-Ischemic ATP-Sensitive Potassium Channel (<i>K</i><sub>ATP</sub>) Opener without Vasorelaxation:  <i>N</i>-(6-Aminobenzopyranyl)-<i>N‘</i>-benzyl-<i>N‘ ‘</i>-cyanoguanidine Analogue
    作者:Sung-eun Yoo、Kyu Yang Yi、Sunkyung Lee、Jeehee Suh、Nakjeong Kim、Byung Ho Lee、Ho Won Seo、Sun-Ok Kim、Dong-Ha Lee、Hong Lim、Hwa Sup Shin
    DOI:10.1021/jm010183f
    日期:2001.11.1
    This paper describes the design, synthesis, and biological evaluation of a novel anti-ischemic compound, (2S,3S,4R)-N-(6-amino-3,4-dihydro-2-dimethoxymethyl-3-hydroxy-2-methyl-2H-benzopyranyl)-N'-benzyl-N " -cyanoguanidine (33), and the structure-activity relationships leading to the discovery of this compound. Compound 33 significantly reduced the myocardial infarct zone to area at risk (IZ/AAR) in the ischemic myocardium rat model with high cardioselectivity. Since the cardioprotective effect of compound 33 is reversed by ATP-sensitive potassium channel (K-ATP) blockers, its anti-ischemic effect appears to be at least mediated by K-ATP opening. In addition, compound 33 shows good protective activity on neuronal cells against oxidative stress, and therefore it is suggested that compound 33 may have therapeutic potential both in cardio- and in neuroprotection.
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