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莫他匹酮 | 90697-57-7

中文名称
莫他匹酮
中文别名
莫大吡酮
英文名称
motapizone
英文别名
6-[4-(1-Imidazolyl)-thien-2-yl]-5-methyl-3-oxo-2,3,4,5-tetrahydro-pyridazine;3-(4-imidazol-1-ylthiophen-2-yl)-4-methyl-4,5-dihydro-1H-pyridazin-6-one
莫他匹酮化学式
CAS
90697-57-7
化学式
C12H12N4OS
mdl
MFCD00865861
分子量
260.319
InChiKey
NPFVRBCDMFKOPY-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):
    1.3
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    87.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4-[4-(1-Imidazolyl)-thien-2-yl]-3-methyl-4-oxobutyronitrile 生成 莫他匹酮
    参考文献:
    名称:
    HILBOLL, G.;PROP, G.;BORBE, H.;LOEHR, J. P.;DOPPALFELD, I. -S.
    摘要:
    DOI:
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文献信息

  • [EN] NOVEL PHTHALAZINONE-PYRROLOPYRIMIDINECARBOXAMIDE DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS DE PHTALAZINONE-PYRROLOPYRIMIDINECARBOXAMIDE
    申请人:NYCOMED GMBH
    公开号:WO2012171900A1
    公开(公告)日:2012-12-20
    The compounds of formula (1), in which R1, R7, R8, R9, R10, R17, R18, R19, R20 and m have the meanings as given in the description, are novel effective inhibitors of type 4 and 5 phosphodiesterase.
    式(1)中的化合物,其中R1、R7、R8、R9、R10、R17、R18、R19、R20和m的含义如描述中所述,是新颖的有效的4型和5型磷酸二酯酶抑制剂
  • NOVEL PHTHALAZINONE-PYRROLOPYRIMIDINECARBOXAMIDE DERIVATIVES
    申请人:Stengel Thomas
    公开号:US20140112945A1
    公开(公告)日:2014-04-24
    The compounds of formula (1) in which R1, R7, R8, R9, R10, R17, R18, R19, R20 and m have the meanings as given in the description, are novel effective inhibitors of type 4 and type 5 phosphodiesterase.
    式(1)中的化合物,其中R1、R7、R8、R9、R10、R17、R18、R19、R20和m的含义如描述中所述,是新颖的有效的磷酸二酯酶4型和5型抑制剂
  • [EN] PHTHALAZINONE-DERIVATIVES AS PDE4 INHIBITORS<br/>[FR] DERIVES DE PHTALAZINONE UTILISES EN TANT QU'INHIBITEURS DE PDE4
    申请人:ALTANA PHARMA AG
    公开号:WO2005075457A1
    公开(公告)日:2005-08-18
    The compounds of a certain formula (1), in which R1, R2, R3, R9 and n have the meanings as given in the description, are novel effective PDE4 inhibitors.
    某种化学式(1)的化合物,其中R1、R2、R3、R9和n的含义如描述中所示,是新型有效的PDE4抑制剂
  • Nicotinamide benzofused-heterocyclyl derivatives useful as selective inhibitors of pde4 isozymes
    申请人:——
    公开号:US20030186989A1
    公开(公告)日:2003-10-02
    Compounds useful as inhibitors of PDE4 in the treatment of diseases regulated by the activation and degranulation of eosinophils, especially asthma, chronic bronchitis, and chronic obstructive pulmonary disease, of Formula (1.0.0): 1 wherein R 5 and R 6 are taken together to form a moiety of partial Formulas (1.1.1) through (1.1.5): 2 or a pharmaceutically acceptable salt thereof.
    在治疗由嗜酸性粒细胞的激活和脱颗粒调节的疾病,特别是哮喘、慢性支气管炎和慢性阻塞性肺病中作为PDE4抑制剂有用的化合物,其化学式为(1.0.0): 其中R5和R6一起取代形成部分化学式(1.1.1)至(1.1.5)的基团, 或其药用可接受的盐。
  • Nitrosated and nitrosylated diuretic compounds, compositions and methods of use
    申请人:Garvey S. David
    公开号:US20050059655A1
    公开(公告)日:2005-03-17
    The invention describes novel nitrosated and/or nitrosylated diuretic compounds or pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated diuretic compound, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides novel compositions and kits comprising at least one diuretic compound of the invention, that is optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating conditions resulting from excessive water and/or electrolyte retention; (b) treating cardiovascular diseases; (c) treating renovascular diseases; (d) treating diabetes; (e) treating diseases resulting from oxidative stress; (f) treating endothelial dysfunctions; (g) treating diseases caused by endothelial dysfunctions; (h) treating cirrhosis; (j) treating pre-eclampsia; (k) treating osteoporosis; and (l) treating nephropathy.
    该发明描述了新颖的亚硝基化和/或亚硝酰化利尿化合物或其药用盐,以及包含至少一种亚硝基化和/或亚硝酰化利尿化合物的新型组合物,以及可选地至少一种一氧化氮供体和/或至少一种治疗剂。该发明还提供了包含该发明中至少一种利尿化合物的新型组合物和试剂盒,该利尿化合物可选择地亚硝基化和/或亚硝酰化,并且可选地至少一种一氧化氮供体化合物和/或至少一种治疗剂。该发明还提供了用于(a)治疗由于过多分和/或电解贮留引起的疾病;(b)治疗心血管疾病;(c)治疗肾血管疾病;(d)治疗糖尿病;(e)治疗由氧化应激引起的疾病;(f)治疗内皮功能障碍;(g)治疗由内皮功能障碍引起的疾病;(h)治疗肝硬化;(j)治疗子痫前期;(k)治疗骨质疏松症;和(l)治疗肾病的方法。
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