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(4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸 | 57153-43-2

中文名称
(4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸
中文别名
——
英文名称
(4-methyl-6,7-dihydro-4H-thieno[3,2-c]pyran-4-yl)-acetic acid
英文别名
(4-Methyl-6,7-dihydro-4h-thieno[3,2-c]pyran-4-yl)acetic acid;2-(4-methyl-6,7-dihydrothieno[3,2-c]pyran-4-yl)acetic acid
(4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸化学式
CAS
57153-43-2
化学式
C10H12O3S
mdl
MFCD01850960
分子量
212.269
InChiKey
MBZWBAMMUGJINB-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

  • 熔点:
    92.5 °C

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    74.8
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2934999090

SDS

SDS:deda9366d11633e593a48c8b9e4e0be5
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反应信息

  • 作为产物:
    描述:
    2-噻吩乙醇 、 alkaline earth salt of/the/ methylsulfuric acid 在 三氟化硼乙醚 作用下, 以 甲苯 为溶剂, 反应 3.0h, 以50%的产率得到(4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸
    参考文献:
    名称:
    Unterhalt; Kissenbeck, Scientia Pharmaceutica, 1999, vol. 67, # 2, p. 97 - 102
    摘要:
    DOI:
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文献信息

  • [EN] 1- (2H-PYRAZOL -3-YL) -3YL) {4-`1- (BENZOYL) -PIPERIDIN-4-YLMETHYL!-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF IMFLAMMATIONS<br/>[FR] DERIVES DE 1-(2H-PYRAZOL-3-YL)-3-{4-`1-(BENZOYL)-PIPERIDIN-4-YLMETHYL!-PHENYL}-UREE ET COMPOSES ASSOCIES UTILISES COMME INHIBITEURS DE LA KINASE P38 ET/OU COMME INHIBITEURS DU FACTEUR DE NECROSE TUMORALE (TNF) DANS LE TRAITEMENT DES INFLAMMATIONS
    申请人:AVENTIS PHARMA INC
    公开号:WO2004100946A1
    公开(公告)日:2004-11-25
    The present invention provides compounds of Formula (I) Wherein ( ) is an optional ethylene bridge; R1 is alkyl, cycloalkyl, aryl or aryl substituted with one or more substituents selected from alkyl, alkoxy and amino, or R1 is pyridyl or pyridyl substituted with one or more substituents selected from alkyl, alkoxy and amino; R2 is optionally substituted alkyl, alkoxyalkyl, optionally substituted cycloalkylalkyl, arylalkyl, or R2 is arylalkyl substituted with one or more substituents selected from alkyl, alkoxy; X is -C(O)-, -C(O)-CH2-, -S(O)2-, or NH-C(O)- ; and A is optionally substituted alkyl or other substituents as defined in claim 1. Pharmaceutical compositions comprising such compounds, their preparation, and their pharmaceutical use in the treatment of disease states capable of being modulated by the inhibition of p38 kinase and/or tumor necrosis factor (TNF), such as asthma or joint inflammation.
    本发明提供了Formula (I)的化合物,其中( )是可选的乙烯桥;R1是烷基、环烷基、芳基或芳基,其上取代基可为烷基、烷氧基和基中的一种或多种,或者R1是吡啶基或吡啶基,其上取代基可为烷基、烷氧基和基中的一种或多种;R2是可选取代的烷基、烷氧基烷基、可选取代的环烷基烷基、芳基烷基,或者R2是芳基烷基,其上取代基可为烷基、烷氧基中的一种或多种;X是-C(O)-、-C(O)-CH2-、-S(O)2-或NH-C(O)-;A是可选取代的烷基或其他在权利要求1中定义的取代基。包括这些化合物的药物组合物、其制备以及在治疗能够通过抑制p38激酶和/或肿瘤坏死因子(TNF)调节的疾病状态中的药用,如哮喘或关节炎。
  • Pyrazoles as inhibitors of tumor necrosis factor
    申请人:Borcherding R. David
    公开号:US20060063796A1
    公开(公告)日:2006-03-23
    The present invention provides compounds of Formula (I) and ester prodrugs, pharmaceutically acceptable salts or solvates of such compounds; or ester prodrugs of such salts or solvates; pharmaceutical compositions comprising such compounds, their preparation, and their pharmaceutical use in the treatment of disease states capable of being modulated by the inhibition of p38 kinase and/or tumor necrosis factor (TNF).
    本发明提供了式(I)的化合物和酯前药、这些化合物的药学上可接受的盐或溶剂;或这些盐或溶剂的酯前药;包括这些化合物的制药组合物,其制备以及它们在治疗能够通过抑制p38激酶和/或肿瘤坏死因子(TNF)调节的疾病状态中的药物应用。
  • 1-(2H-PYRAZOL-3-YL)-3-{4-[1-(BENZOYL)-PIPERIDIN-4-YLMETHYL]-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS
    申请人:Aventis Pharmaceuticals, Inc.
    公开号:EP1622610B1
    公开(公告)日:2006-12-20
  • EP1622610A1
    申请人:——
    公开号:EP1622610A1
    公开(公告)日:2006-02-08
  • US7541368B2
    申请人:——
    公开号:US7541368B2
    公开(公告)日:2009-06-02
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同类化合物

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