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dimethyl 1,2,6-trimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylate | 296899-56-4

中文名称
——
中文别名
——
英文名称
dimethyl 1,2,6-trimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylate
英文别名
dimethyl 1,2,6-trimethyl-4-(3-piridinyl)-1,4-dihydropyridine-3,5-dicarboxylate;Pyridine-3,5-dicarboxylic acid, 1,4-dihydro-1,2,6-trimethyl-4-(3-pyridyl)-, dimethyl ester;dimethyl 1,2,6-trimethyl-4-pyridin-3-yl-4H-pyridine-3,5-dicarboxylate
dimethyl 1,2,6-trimethyl-4-(3-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylate化学式
CAS
296899-56-4
化学式
C17H20N2O4
mdl
MFCD01874529
分子量
316.357
InChiKey
GIGAAERNMQKQOI-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):
    1.6
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    68.7
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • 1,4- DIHYDROPYRIDINE DERIVATIVES WITH HSP MODULATING ACTIVITY
    申请人:LIPIDART KUTATÓ FEJLESZTÖ ÉS TANÁCSADÓ KFT.
    公开号:US20140315893A1
    公开(公告)日:2014-10-23
    The invention provides 1,4-dihydropyridine derivatives of formula (I) wherein R 1 is optionally substituted C 6-24 aryl group or 5 to 6 membered heteroaryl group comprising 1 to 3 nitrogen atoms or other heteroatoms like oxygen and sulphur, and combinations thereof; R 2 and R 3 are independently hydrogen or C 1-6 alkyl group; R 4 and R 5 are independently hydrogen, C 1-6 alkyl group optionally substituted with amino, mono- or di(C 1-6 alkyl)amino, or with 5 to 24 membered optionally fused heterocyclic ring attached by nitrogen and optionally comprising additional 1 to 3 N, O, S heteroatoms and optionally substituted with C 1-6 alkyl group or C 1-6 alkoxy group; R 6 is C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkylC 1-6 alkyl or arylC 1-6 alkyl group; and stereoisomers including enantiomers, diastereomers, racemic mixtures, mixture of enantiomers and combination thereof, as well as polymorphs, pharmaceutically acceptable salts, solvates, esters and prodrugs thereof for use in the therapeutic or prophylactic treatment of a disorder mediated by heat shock proteins.
    本发明提供了式(I)的1,4-二氢吡啶衍生物,其中R1是可选择取代的C6-24芳基或含有1至3个氮原子或其他杂原子(如氧和硫)的5至6成员杂芳基,以及它们的组合;R2和R3分别是氢或C1-6烷基;R4和R5分别是氢,C1-6烷基(可选择取代氨基,单-或双(C1-6烷基)氨基)或带有氮原子的5至24成员可选择融合的杂环,该杂环可选择包含附加的1至3个N、O、S杂原子并可选择取代C1-6烷基或C1-6烷氧基;R6是C1-6烷基,C3-7环烷基,C3-7环烷基C1-6烷基或芳基C1-6烷基;以及立体异构体,包括对映异构体,顺反异构体,混合对映体和它们的组合,以及其药物学上可接受的盐,溶剂化合物,酯和前药,用于治疗或预防由热休克蛋白介导的疾病。
  • 1,4-dihydropyridine derivatives with Hsp modulating activity
    申请人:RICHTER GEDEON NYRT.
    公开号:US10258498B2
    公开(公告)日:2019-04-16
    The invention provides 1,4-dihydropyridine derivatives of formula (I) wherein R1 is optionally substituted C6-24aryl group or 5 to 6 membered heteroaryl group comprising 1 to 3 nitrogen atoms or other heteroatoms like oxygen and sulphur, and combinations thereof; R2 and R3 are independently hydrogen or C1-6alkyl group; R4 and R5 are independently hydrogen, C1-6alkyl group optionally substituted with amino, mono- or di(C1-6alkyl)amino, or with 5 to 24 membered optionally fused heterocyclic ring attached by nitrogen and optionally comprising additional 1 to 3 N, O, S heteroatoms and optionally substituted with C1-6alkyl group or C1-6 alkoxy group; R6 is C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkylC1-6alkyl or arylC1-6alkyl group; and stereoisomers including enantiomers, diastereomers, racemic mixtures, mixture of enantiomers and combination thereof, as well as polymorphs, pharmaceutically acceptable salts, solvates, esters and prodrugs thereof for use in the therapeutic or prophylactic treatment of a disorder mediated by heat shock proteins.
    本发明提供了式(I)的1,4-二氢吡啶衍生物,其中R1是任选取代的C6-24芳基或包含1-3个氮原子或其他杂原子(如氧和硫)的5-6成员杂芳基及其组合;R2和R3独立地为氢或C1-6烷基;R4 和 R5 独立地为氢、任选被氨基、一或二(C1-6-烷基)氨基取代的 C1-6 烷基、或由氮连接的 5 至 24 个成员的任选融合杂环,并任选包含 1 至 3 个 N、O、S 杂原子和任选被 C1-6 烷基或 C1-6 烷氧基取代;R6是C1-6烷基、C3-7环烷基、C3-7环烷基C1-6烷基或芳基C1-6烷基;以及立体异构体,包括对映体、非对映体、外消旋混合物、对映体混合物及其组合,以及其多晶型、药学上可接受的盐、溶液剂、酯和原药,用于治疗或预防由热休克蛋白介导的疾病。
  • 1,4-dihydropyridine derivatives with HSP modulating activity
    申请人:Richter Gedeon NYRT.
    公开号:US10660789B2
    公开(公告)日:2020-05-26
    The invention provides 1,4-dihydropyridine derivatives of formula (I) wherein R1 is optionally substituted C6-24aryl group or 5 to 6 membered heteroaryl group comprising 1 to 3 nitrogen atoms or other heteroatoms like oxygen and sulphur, and combinations thereof; R2 and R3 are independently hydrogen or C1-6alkyl group; R4 and R5 are independently hydrogen, C1-6alkyl group optionally substituted with amino, mono- or di(C1-6alkyl)amino, or with 5 to 24 membered optionally fused heterocyclic ring attached by nitrogen and optionally comprising additional 1 to 3 N, O, S heteroatoms and optionally substituted with C1-6alkyl group or C1-6 alkoxy group; R6 is C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkylC1-6alkyl or arylC1-6alkyl group; and stereoisomers including enantiomers, diastereomers, racemic mixtures, mixture of enantiomers and combination thereof, as well as polymorphs, pharmaceutically acceptable salts, solvates, esters and prodrugs thereof for use in the therapeutic or prophylactic treatment of a disorder mediated by heat shock proteins.
    本发明提供了式(I)的1,4-二氢吡啶衍生物,其中R1是任选取代的C6-24芳基或包含1-3个氮原子或其他杂原子(如氧和硫)的5-6成员杂芳基及其组合;R2和R3独立地为氢或C1-6烷基;R4 和 R5 独立地为氢、任选被氨基、一或二(C1-6-烷基)氨基取代的 C1-6 烷基、或由氮连接的 5 至 24 个成员的任选融合杂环,并任选包含 1 至 3 个 N、O、S 杂原子和任选被 C1-6 烷基或 C1-6 烷氧基取代;R6是C1-6烷基、C3-7环烷基、C3-7环烷基C1-6烷基或芳基C1-6烷基;以及立体异构体,包括对映体、非对映体、外消旋混合物、对映体混合物及其组合,以及其多晶型、药学上可接受的盐、溶液剂、酯和原药,用于治疗或预防由热休克蛋白介导的疾病。
  • 1,4-Dihydropyridine Derivatives With HSP Modulating Activity
    申请人:Richter Gedeon NYRT.
    公开号:US20190192336A1
    公开(公告)日:2019-06-27
    The invention provides 1,4-dihydropyridine derivatives of formula (I) wherein R 1 is optionally substituted C 6-24 aryl group or 5 to 6 membered heteroaryl group comprising 1 to 3 nitrogen atoms or other heteroatoms like oxygen and sulphur, and combinations thereof; R 2 and R 3 are independently hydrogen or C 1-6 alkyl group; R 4 and R 5 are independently hydrogen, C 1-6 alkyl group optionally substituted with amino, mono- or di(C 1-6 alkyl)amino, or with 5 to 24 membered optionally fused heterocyclic ring attached by nitrogen and optionally comprising additional 1 to 3 N, O, S heteroatoms and optionally substituted with C 1-6 alkyl group or C 1-6 alkoxy group; R 6 is C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkylC 1-6 alkyl or arylC 1-6 alkyl group; and stereoisomers including enantiomers, diastereomers, racemic mixtures, mixture of enantiomers and combination thereof, as well as polymorphs, pharmaceutically acceptable salts, solvates, esters and prodrugs thereof for use in the therapeutic or prophylactic treatment of a disorder mediated by heat shock proteins.
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