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4-hydroxy-2-(naphthoylamino)-benzoic acid methyl ester | 848826-18-6

中文名称
——
中文别名
——
英文名称
4-hydroxy-2-(naphthoylamino)-benzoic acid methyl ester
英文别名
2-(2-naphthoylamino)4-hydroxybenzoic acid methyl ester;Methyl 4-hydroxy-2-(naphthalene-2-carbonylamino)benzoate
4-hydroxy-2-(naphthoylamino)-benzoic acid methyl ester化学式
CAS
848826-18-6
化学式
C19H15NO4
mdl
——
分子量
321.332
InChiKey
ZZJLFXBPPYWOOS-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):
    4.1
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • SUBSTITUTED ARYL OXIMES
    申请人:Havran Lisa Marie
    公开号:US20080293790A1
    公开(公告)日:2008-11-27
    The present invention relates to substituted aryl oximes and methods of using them.
    本发明涉及取代芳基肟及其使用方法。
  • 4-(PHENYL-ETHYLIDENEAMINOXY-PROPOXY)-PHENYL-ACETIC ACID DERIVATIVES AND RELATED COMPOUNDS AS PAI-1 INHIBITORS FOR THE TREATMENT OF IMPAIREMENT OF THE FIBRINOLYTIC SYSTEM AND OF THROMBISIS
    申请人:Wyeth
    公开号:EP1663189A1
    公开(公告)日:2006-06-07
  • US7420083B2
    申请人:——
    公开号:US7420083B2
    公开(公告)日:2008-09-02
  • [EN] 4-(PHENYL-ETHYLIDENEAMINOXY-PROPOXY) -PHENYL-ACETIC ACID DERIVATIVES AND RELATED COMPOUNDS AS PAI-1 INHIBITORS FOR THE TREATMENT OF IMPAIRMENT OF THE FIBRINOLYTIC SYSTEM AND OF THROMBOSIS<br/>[FR] DERIVES D'ACIDE 4-(PHENYL-ETHYLIDENEAMINOXY-PROPOXY)-PHENYL-ACETIQUE ET COMPOSES CORRESPONDANTS UTILISES COMME INHIBITEURS DE PAI-1 PERMETTANT DE TRAITER UNE DEFICIENCE DU SYSTEME FIBRINOLYTIQUE ET LA THROMBOSE
    申请人:WYETH CORP
    公开号:WO2005030193A1
    公开(公告)日:2005-04-07
    The present invention relates to substituted aryl oximes of formula (I) or a pharmaceutically acceptable salt or ester form thereof wherein R1 is a direct bond to A, C1-C4 alkylene, or -O-C1-C4 alkylene; R2 and R3 are , independently hydrogen, halogen, C1-C4 alkyl, C1-C3 perfluoroalkyl, -O-C1-C3 perfluoroalkyl, C1-C3 alkoxy, -OH, -NH2, -NO2, -O(CH2)p-aryl, -O(CH2)p-heteroaryl, aryl, heteroaryl, -NH(CH2)p-aryl, -NH(CH2)p-heteroaryl, -NH(CO)-aryl, -NH(CO)-heteroaryl, -O(CO)-aryl, -O(CO)-heteroaryl, -NH(CO)-CH=CH-aryl, or -NH(CO)-CH=CH-heteroaryl; p is an integer from 0-6; R4 is hydrogen, C1-C8 alkyl, or C3-C6 cycloalkyl; A is COOH or an acid mimic; X is C1-C8 alkylene, C3-C6 cycloalkylene, -(CH2)mO-, or -(CH2)mNH-; m is an integer from 1-6; R5 and R6 are, independently, hydrogen, halogen, C1-C6 alkyl, C1-C6 perfluoroalkyl, -O-C1-C6 perfluoroalkyl, C1-C6 alkoxy, -OH, -NH2, -NO2, -O(CH2)n-aryl, O(CH2)n-heteroaryl, aryl, or heteroaryl; and is an integer from 0-6, wherein C1-C4 alkaline, -O-C1-C4 alkaline, alkyl, aryl and heteroaryl are each optionally substituted by one or more substituents. The present compounds are PAI-1 inhibitors for the treatment e.g of impairment of the fibrinolytic system, thrombosis or cardiovascular diseases.
  • Substituted aryloximes
    申请人:Havran Marie Lisa
    公开号:US20050070584A1
    公开(公告)日:2005-03-31
    The present invention relates to substituted aryl oximes and methods of using them.
    本发明涉及取代的芳香基氧化亚氮及其使用方法。
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