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3-[3-amino-4-(indan-2-yloxy)-5-(1H-indazol-5-yl)phenyl]propionic acid | 590415-93-3

中文名称
——
中文别名
——
英文名称
3-[3-amino-4-(indan-2-yloxy)-5-(1H-indazol-5-yl)phenyl]propionic acid
英文别名
3-[3-amino-4-(2,3-dihydro-1H-inden-2-yloxy)-5-(1H-indazol-5-yl)phenyl]propanoic acid
3-[3-amino-4-(indan-2-yloxy)-5-(1H-indazol-5-yl)phenyl]propionic acid化学式
CAS
590415-93-3
化学式
C25H23N3O3
mdl
——
分子量
413.476
InChiKey
ODWAUDKBHMPLAW-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):
    4.3
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    101
  • 氢给体数:
    3
  • 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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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-(+)-5,5'',6,6'',7,7'',8,8''-八氢-3,3''-二叔丁基-1,1''-二-2-萘酚,双钾盐 (S)-盐酸沙丁胺醇 (S)-溴烯醇内酯 (S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2-N-Fmoc-氨基甲基吡咯烷盐酸盐 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-3-(叔丁基)-4-(2,6-二异丙氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-3,3''-双([[1,1''-联苯]-4-基)-[1,1''-联萘]-2,2''-二醇 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-2,2'',3,3''-四氢-6,6''-二-9-菲基-1,1''-螺双[1H-茚]-7,7''-二醇 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (6,6)-苯基-C61己酸甲酯 (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,5R)-3,3a,8,8a-四氢茚并[1,2-d]-1,2,3-氧杂噻唑-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aS,8aR)-2-(吡啶-2-基)-8,8a-二氢-3aH-茚并[1,2-d]恶唑 (3aS,3''aS,8aR,8''aR)-2,2''-环戊二烯双[3a,8a-二氢-8H-茚并[1,2-d]恶唑] (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (3S,3aR)-2-(3-氯-4-氰基苯基)-3-环戊基-3,3a,4,5-四氢-2H-苯并[g]吲唑-7-羧酸 (3R,3’’R,4S,4’’S,11bS,11’’bS)-(+)-4,4’’-二叔丁基-4,4’’,5,5’’-四氢-3,3’’-联-3H-二萘酚[2,1-c:1’’,2’’-e]膦(S)-BINAPINE (3-三苯基甲氨基甲基)吡啶 (3-[(E)-1-氰基-2-乙氧基-2-hydroxyethenyl]-1-氧代-1H-茚-2-甲酰胺) (2′′-甲基氨基-1,1′′-联苯-2-基)甲烷磺酰基铝(II)二聚体 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,4S)-Fmoc-4-三氟甲基吡咯烷-2-羧酸 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环