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5-[3-methoxy-4-(1,1,2-trifluoroethoxy)phenyl]-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one

中文名称
——
中文别名
——
英文名称
5-[3-methoxy-4-(1,1,2-trifluoroethoxy)phenyl]-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one
英文别名
6-Ethyl-5-[3-methoxy-4-(1,1,2-trifluoroethoxy)phenyl]-3,6-dihydro-1,3,4-thiadiazin-2-one
5-[3-methoxy-4-(1,1,2-trifluoroethoxy)phenyl]-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one化学式
CAS
——
化学式
C14H15F3N2O3S
mdl
——
分子量
348.346
InChiKey
RXMMEOLLNAJJSC-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):
    4
  • 重原子数:
    23
  • 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:
    85.2
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • Use of phosphodiesterase iv inhibitors
    申请人:——
    公开号:US20040235845A1
    公开(公告)日:2004-11-25
    Use of phosphodiesterase IV inhibitors and/or physiologically acceptable salts thereof for the preparation of a medicament for the treatment of osteoporosis, tumours, tumour metastases, atherosclerosis, rheumatoid arthritis, multiple sclerosis, diabetes mellitus, ulcerative collitis and AIDS.
    将磷酸二酯酶 IV 抑制剂和/或其生理上可接受的盐用于制备治疗骨质疏松症、肿瘤、肿瘤转移、动脉粥样硬化、类风湿性关节炎、多发性硬化、糖尿病、溃疡性结肠炎和艾滋病的药物。
  • Thiadiazinone und sie enthaltende Arzneimittel, insbesondere mit Positiv-Inotroper und vasodilatierender Wirksamkeit
    申请人:MERCK PATENT GmbH
    公开号:EP0539806B1
    公开(公告)日:1995-01-04
  • Type 4 phosphodiesterase inhibitors and uses thereof
    申请人:——
    公开号:US20040259863A1
    公开(公告)日:2004-12-23
    The invention relates to the use of type 4 phosphodiesterase inhibitors (PDE IV inhibitors) to treat diseases and to combinations of PDE IV inhibitors with other drugs.
  • Differentiation modulating agents and uses therefor
    申请人:Prins Bernhard Johannes
    公开号:US20050282733A1
    公开(公告)日:2005-12-22
    The present invention is directed to methods and agents for modulating the differentiation potential and/or proliferation of preadipocytes. More particularly, the present invention discloses methods and agents for modulating a fibroblast growth factor (FGF) signaling pathway, especially the FGF-1 or FGF-2 signaling pathway, for treating or preventing adiposity-related conditions including, but not limited to, obesity, lipoma, lipomatosis, cachexia or lipodystrophy or the loss of adipose tissue in trauma or atrophic conditions.
  • DIFFERENTIATION MODULATING AGENTS AND USES THEREFOR
    申请人:Prins Johannes Bernhard
    公开号:US20120059047A1
    公开(公告)日:2012-03-08
    The present invention is directed to methods and agents for modulating the differentiation potential and/or proliferation of preadipocytes. More particularly, the present invention discloses methods and agents for modulating a fibroblast growth factor (FGF) signaling pathway, especially the FGF-1 or FGF-2 signaling pathway, for treating or preventing adiposity-related conditions including, but not limited to, obesity, lipoma, lipomatosis, cachexia or lipodystrophy or the loss of adipose tissue in trauma or atrophic conditions.
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