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3-(4-(4-(5-(1-ethyl-6,6-dimethyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)piperazin-1-yl)propanoic acid | 1233242-46-0

中文名称
——
中文别名
——
英文名称
3-(4-(4-(5-(1-ethyl-6,6-dimethyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)piperazin-1-yl)propanoic acid
英文别名
3-[4-[4-[5-(1-ethyl-6,6-dimethyl-5,7-dihydro-4H-indazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl]piperazin-1-yl]propanoic acid
3-(4-(4-(5-(1-ethyl-6,6-dimethyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)piperazin-1-yl)propanoic acid化学式
CAS
1233242-46-0
化学式
C26H34N6O3
mdl
——
分子量
478.594
InChiKey
JRLXBUATYGNKBD-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):
    1.3
  • 重原子数:
    35
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    101
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • 1,2,4-oxadiazole derivatives and their therapeutic use
    申请人:Laboratorios Almirall, S.A.
    公开号:EP2202232A1
    公开(公告)日:2010-06-30
    New derivatives of general formula (I), or pharmaceutically acceptable salts or N-oxides thereof wherein, A is selected from the group consisting of -N-, -O- and -S-; B and C are independently selected from the group consisting of-N- and -O-, with the proviso that at least two of A, B and C are nitrogen atoms; G1 is selected from the group consisting of -CH2-, -NH- and -O-; G2 is selected from the group consisting of -NR4- and -O-; R1 represents: ➢ a 8 to 10 membered bicyclic N-containing heteroaryl group optionally substituted with a C1-4 carboxyalkyl group or a C1-4 aminoalkyl group, ➢ a pyridyl group optionally substituted with one or more substituents selected from hydroxy groups, C1-4 alkyl groups, C1-4 carboxyalkyl groups, C1-4 haloalkyl groups, C1-4 alkoxy groups, amino groups, C1-4 aminoalkyl groups and C1-4 aminoalkoxy groups, ➢ a pyridone group substituted with one or more C1-4 alkyl groups; C1-4 haloalkyl groups or C1-4 aminoalkyl groups, or ➢ a group of formula: wherein: • Ra represents a hydrogen atom, a halogen atom, a C1-4 alkyl group, C3-4 cycloalkyl group or a -CF3 group; • Rb represents a hydrogen atom, a halogen atom, a C14 alkyl group, a -CF3 group or a C1-4 alkoxy group; • Rd represents a hydrogen atom, a C1-4 alkyl group or a C1-4 alkoxy group; • Rc represents: ○ a hydrogen atom, a C1-4 hydroxyalkyl group, a C1-4 aminoalkyl group which is optionally substituted with one or more substituents selected from halogen atoms, hydroxy groups and -CF3 groups; ○ a 4 to 6-membered saturated N-containing heterocyclic ring optionally substituted with a C1-2 carboxyalkyl group; ○ -(CH2)(0-4)-C(O)OR', -(CH2)(0-4)-C(O)NR'R", -(CH2)(0-4)-NHC(O)R", -S(O)2NR'R", -O-(CH2)(2-4)NR'R", -O-(CH2)(1-4)C(O)OR", -O-(CH2)(1-4)-C(O)NR'R", -(CH2)(0-4)-NR'R", -(CH2)(0-4)-CONHS(O)2R', -(CH2)(0-4)-NHS(O)2R' or -(CH2)(0-3)-N H-(CH2)(1-3)-(NH)(0-1)S(O)2R' wherein, ■ R' represents a hydrogen atom or a C1-4 alkyl group, ■ R" represents a hydrogen atom, a C1-4 alkyl group, a C3-4 cycloalkyl group, a C1-4 carboxyalkyl group, a C1-4 haloalkyl group, a C1-4 hydroxyalkyl group or a 6 membered, saturated N-containing heterocyclic ring, or ■ R' and R" together with the nitrogen atom to which they are attached from a 4 to 6 membered heterocyclic group which contains, as heteroatoms, one N atom and, optionally, one further atom selected from N and O, and which is optionally substituted with a carboxy or a C1-4 carboxyalkyl group, or Rc together with Rd form a C5-6 cycloalkyl group optionally substituted by a -NHRf group, wherein Rf is selected from the group consisting of a hydrogen atom and a carboxymethyl group; R2 and R3 are independently selected from the group consisting of hydrogen atoms, halogen atoms and C1-4 alkyl groups; and R4 is selected from the group consisting of a hydrogen atom, a phenyl group, a C3-4 cycloalkyl-C1-4 alkyl group, C1-4 aminoalkyl group, C1-4 haloalkyl group and a linear or branched C1-4 alkyl group which is optionally substituted by a phenyl or a pyridyl group.
    通用公式(I)的新衍生物,或其药用可接受盐或N-氧化物,其中, A选自-N-,-O-和-S-组成的群; B和C分别选自-N-和-O-组成的群,但至少有两个A,B和C是氮原子; G1选自-CH2-,-NH-和-O-组成的群; G2选自-NR4-和-O-组成的群; R1代表: ➢一个含氮杂环的8到10成员双环基团,可选择地取代为C1-4羧基烷基基团或C1-4基烷基基团, ➢一个吡啶基,可选择地取代为一个或多个取代基,所选取代基包括羟基、C1-4烷基基团、C1-4羧基烷基基团、C1-4卤代烷基基团、C1-4烷氧基团、基、C1-4基烷基基团和C1-4氧基团, ➢一个吡啶酮基,取代为一个或多个C1-4烷基基团;C1-4卤代烷基基团或C1-4基烷基基团,或 ➢一个公式的基团: 其中: • Ra代表氢原子、卤原子、C1-4烷基基团、C3-4环烷基基团或-CF3基团; • Rb代表氢原子、卤原子、C14烷基基团、- 基团或C1-4烷氧基团; • Rd代表氢原子、C1-4烷基基团或C1-4烷氧基团; • Rc代表: ○氢原子、C1-4羟基烷基基团、C1-4基烷基基团,可选择地取代为一个或多个取代基,所选取代基包括卤原子、羟基和- 基团; ○一个4到6成员饱和的含氮杂环环,可选择地取代为C1-2羧基烷基基团; ○-( )(0-4)-C(O)OR',-( )(0-4)-C(O)NR'R",-( )(0-4)-NHC(O)R",-S(O)2NR'R",-O-( )(2-4)NR'R",-O-( )(1-4)C(O)OR",-O-( )(1-4)-C(O)NR'R",-( )(0-4)-NR'R",-( )(0-4)-CONHS(O)2R',-( )(0-4)-NHS(O)2R'或-( )(0-3)-N H-( )(1-3)-(NH)(0-1)S(O)2R'其中, ■ R'代表氢原子或C1-4烷基基团, ■ R"代表氢原子、C1-4烷基基团、C3-4环烷基基团、C1-4羧基烷基基团、C1-4卤代烷基基团、C1-4羟基烷基基团或6成员饱和的含氮杂环环,或 ■ R'和R"与它们连接的氮原子一起形成一个4到6成员的杂环基团,该基团包含一个N原子和可选择地一个进一步选择自N和O的原子,并可选择地取代为羧基或C1-4羧基烷基基团, 或Rc与Rd一起形成一个可选择地由-NHRf基团取代的C5-6环烷基基团,其中Rf选自氢原子和羧甲基基团; R2和R3分别选自氢原子、卤原子和C1-4烷基基团;和 R4选自氢原子、苯基团、C3-4环烷基-C1-4烷基基团、C1-4基烷基基团、C1-4卤代烷基基团和可选择地由苯基或吡啶基取代的线性或支链C1-4烷基基团。
  • 1,2,4-OXADIAZOLE DERIVATIVES AND THEIR THERAPEUTIC USE
    申请人:Giulio Matassa Victor
    公开号:US20110311485A1
    公开(公告)日:2011-12-22
    The present disclosure relates to 1, 2, 4 oxadiazole derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the S1P1 receptors.
    本公开涉及公式(I)的1,2,4-噁二唑衍生物,以及包含它们的药物组合物,以及它们作为S1P1受体激动剂在治疗中的使用。
  • S1P1 receptor agonists for use in the treatment of multiple sclerosis
    申请人:Almirall, S.A.
    公开号:EP2455080A1
    公开(公告)日:2012-05-23
    a S1 P1 receptor agonist of formula (I), or a pharmaceutically acceptable salt, or solvate, or N-oxide, or stereoisomer or deuterated derivate thereof, alone or combined with IFNβ, for use in the treatment of multiple sclerosis disease.
    式(I)的 S1 P1 受体激动剂,或其药学上可接受的盐、或溶液剂、或 N-氧化物、或立体异构体或代衍生物,单独或与 IFNβ合用,用于治疗多发性硬化症疾病。
  • S1P1 receptor agonists for use in the treatment of crohn's disease
    申请人:Almirall, S.A.
    公开号:EP2455081A1
    公开(公告)日:2012-05-23
    a S1P1 receptor agonist of formula (I), or a pharmaceutically acceptable salt, or solvate, or N-oxide, or stereoisomer or deuterated derivate thereof, for use in the treatment of inflammatory bowel disease, in particular Crohn's disease.
    式(I)的 S1P1 受体激动剂或其药学上可接受的盐、或溶液剂、或 N-氧化物、或立体异构体或代衍生物,用于治疗炎症性肠病,尤其是克罗恩病。
  • 1, 2, 4 -OXADIAZOLE DERIVATIVES AND THEIR THERAPEUTIC USE
    申请人:Almirall S.A.
    公开号:EP2370431A1
    公开(公告)日:2011-10-05
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