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3-[3-amino-5-(1-ethyl-1H-indazol-5-yl)-4-(indan-2-yloxy)phenyl]propionic acid | 590415-96-6

中文名称
——
中文别名
——
英文名称
3-[3-amino-5-(1-ethyl-1H-indazol-5-yl)-4-(indan-2-yloxy)phenyl]propionic acid
英文别名
3-[3-amino-4-(2,3-dihydro-1H-inden-2-yloxy)-5-(1-ethylindazol-5-yl)phenyl]propanoic acid
3-[3-amino-5-(1-ethyl-1H-indazol-5-yl)-4-(indan-2-yloxy)phenyl]propionic acid化学式
CAS
590415-96-6
化学式
C27H27N3O3
mdl
——
分子量
441.53
InChiKey
JLUIPERNESBRPQ-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):
    4.6
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    90.4
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Substituted phenylalkanoic acid derivatives and use thereof
    申请人:——
    公开号:US20040044258A1
    公开(公告)日:2004-03-04
    A compound represented by the formula (I) or a salt thereof: 1 wherein n represents an integer of 1 to 3, R represents an alkyl group having 3 to 8 carbon atoms, a group represented by the following formula: R 1 (CH 2 ) k — (wherein k represents 0 or an integer of 1 to 3; R 1 represents a saturated cyclic alkyl group having 3 to 7 carbon atoms or a saturated condensed cyclic alkyl group having 6 to 8 carbon atoms, and the group R 1 may be substituted with a lower alkyl group having 1 to 4 carbon atoms) and the like, and Ar represents a condensed bicyclic group such as naphthalen-1-yl group, which has suppressing action on prostaglandin and leukotriene production and is useful for prophylactic and/or therapeutic treatment of various inflammatory diseases and the like caused by these lipid mediators.
    化合物的化学式为(I)或其盐: 其中n表示1到3的整数,R表示具有3到8个碳原子的烷基基团,由以下化学式表示的基团:R1(CH2)k—(其中k表示0或1到3的整数;R1表示具有3到7个碳原子的饱和环烷基基团或具有6到8个碳原子的饱和紧凑环烷基基团,基团R1可以被具有1到4个碳原子的较低烷基基团取代)等,Ar表示如-1-基团等的紧凑双环基团,具有对前列腺素白三烯生成的抑制作用,对由这些脂质介质引起的各种炎症性疾病等的预防和/或治疗治疗有用。
  • Novel crystal forms of substituted phenylalkanoic acids and process for producing the same
    申请人:Arimoto Yuichi
    公开号:US20080070967A1
    公开(公告)日:2008-03-20
    [Object] In the case of using 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, or methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate as a medicine, more preferable aspects or improved methods are provided. [Means] Crystals of any compound among 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, and methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate, and methods of producing the same are provided.
    【对象】在使用3- [3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸,甲基3- [4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯或甲基3- [3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯作为药物时,提供了更可取的方面或改进的方法。 【手段】提供了3- [3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸,甲基3- [4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯和甲基3- [3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯中的任何一种化合物的晶体以及制备它们的方法。
  • STABLE PHARMACEUTICAL COMPOSITION
    申请人:SUZUKI Kazumi
    公开号:US20100041725A1
    公开(公告)日:2010-02-18
    A pharmaceutical composition comprising a compound represented by the general formula (I): or a salt thereof, and a pharmaceutically acceptable carrier, wherein the composition does not substantially contain a reducing sugar and/or a carrier containing a reducing sugar as an ingredient as the pharmaceutically acceptable carrier, or when the composition contains a reducing sugar and/or a carrier containing a reducing sugar as an ingredient as the pharmaceutically acceptable carrier, contact of the reducing sugar and the compound represented by the general formula (I) or a salt thereof is eliminated.
    一种药物组合物,包括下列通式(I)所表示的化合物或其盐,以及一种药学上可接受的载体。其中,该组合物不含有可还原糖和/或含有可还原糖的载体作为药学上可接受的载体成分,或者当该组合物含有可还原糖和/或含有可还原糖的载体作为药学上可接受的载体成分时,消除了可还原糖与下列通式(I)所表示的化合物或其盐之间的接触。
  • NOVEL CRYSTALS OF SUBSTITUTED PHENYLALKANOIC ACID AND METHOD OF PRODUCING THE SAME
    申请人:ARIMOTO Yuichi
    公开号:US20090312386A1
    公开(公告)日:2009-12-17
    [Object] In the case of using 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, or methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate as a medicine, more preferable aspects or improved methods are provided. [Means] Crystals of any compound among 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, and methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate, and methods of producing the same are provided.
    【目的】本发明提供使用3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸、甲基3-[4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯或甲基3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯作为药物时,提供更优选的方面或改进的方法。 【手段】本发明提供3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸、甲基3-[4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯和甲基3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯中的任何化合物的晶体以及其制备方法。
  • NOVEL CRYSTAL OF SUBSTITUTED PHENYLALKANOIC ACID ESTER AND PROCESS FOR PRODUCING THE SAME
    申请人:SHODA Motoshi
    公开号:US20100234440A1
    公开(公告)日:2010-09-16
    [Object] In the case of using 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, or methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate as a medicine, more preferable aspects or improved methods are provided. [Means] Crystals of any compound among 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionic acid, methyl 3-[4-(indan-2-yloxy)-3-(1-methyl-1H-indazol-5-yl)-5-nitrophenyl]propionate, and methyl 3-[3-amino-4-(indan-2-yloxy)-5-(1-methyl-1H-indazol-5-yl)phenyl]propionate, and methods of producing the same are provided.
    【对象】在使用3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸、甲基3-[4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯或甲基3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯作为药物时,提供了更可取的方面或改进的方法。 【方法】提供了3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸、甲基3-[4-(-2-氧基)-3-(1-甲基-1H-吲唑-5-基)-5-硝基苯基]丙酸酯和甲基3-[3-基-4-(-2-氧基)-5-(1-甲基-1H-吲唑-5-基)苯基]丙酸酯中的任何化合物的晶体以及其制备方法。
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