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2-[4-(6-Dimethylaminohexyloxy)phenylthio]-3-(2-thenoyl)-pyridine fumarate | 129183-50-2

中文名称
——
中文别名
——
英文名称
2-[4-(6-Dimethylaminohexyloxy)phenylthio]-3-(2-thenoyl)-pyridine fumarate
英文别名
(E)-but-2-enedioic acid;[2-[4-[6-(dimethylamino)hexoxy]phenyl]sulfanylpyridin-3-yl]-thiophen-2-ylmethanone
2-[4-(6-Dimethylaminohexyloxy)phenylthio]-3-(2-thenoyl)-pyridine fumarate化学式
CAS
129183-50-2
化学式
C4H4O4*C24H28N2O2S2
mdl
——
分子量
556.704
InChiKey
QRNZYVFVZDNGKI-WLHGVMLRSA-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):
    5.74
  • 重原子数:
    38
  • 可旋转键数:
    14
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    171
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • Pyridine compounds and pharmaceutical use thereof
    申请人:YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD.
    公开号:EP0359547A1
    公开(公告)日:1990-03-21
    A novel pyridine compound of the formula wherein R¹ and R² are the same or different and respectively mean hydrogen, a halogen, an alkyl, an alkoxy or an optionally substituted phenyl; Ar means an optionally substituted aryl or heteroaryl; Y means a single bond or an alkylene which may have double bond(s) in the chain; W means a group of the formula (wherein R³ and R⁴ are the same or different and respectively mean hydrogen, a halogen, an alkyl, an alkoxy or an optionally substituted phenyl, X means -O-, -S- or -N(R⁵)- (wherein R⁵ means hydrogen, an alkyl or an acyl), Z means a single bond, -O-, -S-, -N(R⁶)- (wherein R⁶ means hydrogen, an alkyl or an acyl) or -CON(R⁷)- (wherein R⁷ means hydrogen, an alkyl or an acyl), A means an alkylene, B means an alkoxycarbonyl, carboxyl, hydroxyl group, -N(R⁸)(R⁹) (wherein R⁸ and R⁹ are the same or different and respectively mean hydrogen, an alkyl, a hydroxyalkyl, an acyl or an optionally substituted aralkyl or heteroaralkyl or conbinedly means a group forming, taken together with the adjacent nitrogen, a heterocyclic group) or -CON(R¹⁰)(R¹¹) (wherein R¹⁰ and R¹¹ are the same or different and respectively mean hydrogen, an alkyl, a hydroxyalkyl, an acyl or an optionally substituted aralkyl or heteroaralkyl, or combinedly mean a group forming, taken together with the adjacent nitrogen, a heterocyclic group), a group of the formula (wherein R¹² and R¹³ are the same or different and respectively mean hydrogen, an alkyl, a hydroxyalkyl, an acyl, an optionally substituted phenyl or an optionally substituted aralkyl or heteroaralkyl, or combinedly mean a group forming, taken together with the adjacent nitrogen atom, a heterocyclic group, P means -O-, -S(O)p- (wherein p means an integer of 0 to 2), -N(R¹⁴)- (wherein R¹⁴ means hydrogen, an alkyl or an acyl) or -N(R¹⁵)CO- (wherein R¹⁵ means hydrogen, an alkyl or an acyl), Q means an alkylene having not less than 5 carbon atoms, a cyclic alkylene, an alkylene having not less than 4 carbon atoms which has an interposing oxygen or a sulfur therein or an alkylene having not less than 5 carbon atoms which has carbonyl group at the terminus, with the proviso that Q means an alkylene having not less than 3 carbon atoms, when P is -N(R¹⁵)CO-) or a group of the formula (wherein n means an integer of 3 to 5), or a salt thereof. The compounds exhibit inhibitory activity on prolylendopeptidase. Also disclosed are pharmaceutical compositions containing the novel pyridine compounds.
    一种新型吡啶化合物,其式如下 其中 R¹ 和 R² 相同或不同,分别表示氢、卤素、烷基、烷氧基或任选取代的苯基;Ar 表示任选取代的芳基或杂芳基;Y 表示单键或链中可能有双键的亚烷基;W 表示式中的基团 (其中 R³ 和 R⁴ 相同或不同,分别指氢、卤素、烷基、烷氧基或任选取代的苯基;X 指 -O-、-S- 或 -N(R⁵)-(其中 R⁵ 指氢、烷基或酰基);Z 指单键、-O-、-S-、-N(R⁶)-(其中 R⁶ 指氢、烷基或酰基)或-CON(R⁷)-(其中 R⁷ 指氢、烷基或酰基),A 指亚烷基、B 表示烷氧基羰基、羧基、羟基、-N(R⁸)(R⁹)(其中 R⁸ 和 R𠞙 相同或不同,分别表示氢、烷基、羟基烷基或酰基)、烷基、羟基烷基、酰基或任选取代的芳烷基或杂烷基,或结合指与邻近的氮一起形成杂环基的基团)或 -CON(R¹⁰)(R¹¹)(其中 R¹⁰ 和 R¹¹ 相同或不同,分别表示氢、烷基、羟基烷基、酰基或任选取代的芳烷基或杂烷基,或与相邻的氮结合形成杂环基的基团),式中的基团 (其中 R¹² 和 R¹³ 相同或不同,分别指氢、烷基、羟基烷基、酰基、任选取代的苯基或任选取代的芳基或杂烷基,或合并指一个基团、P指-O-、-S(O)p-(其中 p 指 0 至 2 的整数)、-N(R¹⁴)-(其中 R¹⁴ 指氢、烷基或酰基)或-N(R¹⁵)CO-(其中 R¹⁵ 指氢、其中 R¹⁵ 指氢、烷基或酰基),Q 指具有不少于 5 个碳原子的亚烷基、环状亚烷基、具有不少于 4 个碳原子的亚烷基(其中有一个中间氧或一个)或具有不少于 5 个碳原子的亚烷基(其末端有羰基),但条件是当 P 为-N(R¹⁵)CO- 时,Q 指具有不少于 3 个碳原子的亚烷基)或式中的基团(其中 n 指整数)。 (其中 n 指 3 至 5 的整数)或其盐。 这些化合物对原内酯肽酶具有抑制活性。还公开了含有新型吡啶化合物的药物组合物。
  • Pyridine compounds for treating amnesia
    申请人:YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD.
    公开号:EP0558094A1
    公开(公告)日:1993-09-01
    A novel compound of the formula wherein R¹ means hydrogen and R² means hydrogen or a straight-chain or branched chain alkyl having 1 to 8 carbon atoms; Ar means phenyl, a phenyl substituted by 1 to 3 substituent(s) selected from among halogens, straight-chain or branched chain alkyls having 1 to 8 carbon atoms, straight-chain or branched chain alkoxys having 1 to 8 carbon atoms, trifluoromethyl, amino, nitro and cyano, furyl, a furyl substituted by 1 to 3 substituent(s) selected from among halogens, straight-chain or branched chain alkyls having 1 to 8 carbon atoms, straight-chain or branched chain alkoxys having 1 to 8 carbon atoms, trifluoromethyl, straight-chain or branched chain alkylthiols having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfinyls having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfonyls having 1 to 8 carbon atoms, amino, nitro and cyano, thienyl, a thienyl substituted by 1 to 3 substituent(s) selected from among halogens, straight-chain or branched chain alkyls having 1 to 8 carbon atoms, straight-chain or branched chain alkoxys having 1 to 8 carbon atoms, trifluoromethyl, straight-chain or branched chain alkylthiols having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfinyls having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfonyls having 1 to 8 carbon atoms, amino, nitro and cyano, pyrrolyl, a pyrrolyl substituted by 1 to 3 substituent(s) selected from among halogens, straight-chain or branched chain alkyls having 1 to 8 carbon atoms, straight-chain or branched chain alkoxys having 1 to 8 carbon atoms, trifluoromethyl, straight-chain or branched chain alkylthiols having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfinyls having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfonyls having 1 to 8 carbon atoms, amino, nitro and cyano, pyridyl, or a pyridyl substituted by 1 to 3 substituent(s) selected from among halogens, straight-chain or branched chain alkyls having 1 to 8 carbon atoms, straight-chain or branched chain alkoxys having 1 to 8 carbon atoms, trifluoromethyl, straight-chain or branched chain alkylthiols having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfinyls having 1 to 8 carbon atoms, straight-chain or branched chain alkylsulfonyls having 1 to 8 carbon atoms, amino, nitro and cyano: Y means a single bond or a straight-chain or branched chain alkylene having 1 to 8 carbon atoms which may have double bond(s) in the chain; W means a group of the formula (i) (wherein R³ and R⁴ are the same or different and respectively mean hydrogen or a halogen, X means -O- or -S-, Z means a single bond or -O-, A is a straight-chain or branched chain alkylene having 1 to 8 carbon atoms, B means -N(R⁸)(R⁹) (wherein R⁸ and R⁹ are the same or different and respectively mean hydrogen or a straight-chain or branched chain alkyl having 1 to 8 carbon atoms, or combinedly means a group forming, taken together with the adjacent nitrogen, 1-pyrrolidinyl, 2-oxo-1-pyrrolidinyl, piperidino, 1-piperazinyl, a 1-piperazinyl substituted by a straight-chain or branched chain alkyl having 1 to 8 carbon atoms at the 4-position, 1-homopiperazinyl, morpholino and thiomorpholino) or a group of the formula (ii) (wherein R¹² and R¹³ are the same or different and respectively mean hydrogen or a straight-chain or branched chain alkyl having 1 to 8 carbon atoms, P is -S- and Q is hexamethylene, heptamethylene, octamethylene, 1-methylpentamethylene, 1-methylhexamethylene, 1-methylheptamethylene, -(CH₂)₂S(CH₂)₃-, -(CH₂)₂S(CH₂)₆-. or a pharmaceutically acceptable salt thereof or a hydrate thereof. The compounds exhibit inhibitory activity on prolylendopeptidase. Also disclosed are pharmaceutical compositions containing the novel pyridine compounds.
    一种新颖的式化合物 其中 R¹ 指氢,R² 指氢或具有 1 至 8 个碳原子的直链或支链烷基;Ar 指苯基、被 1 至 3 个取代基取代的苯基,这些取代基选自卤素、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷氧基、三甲基、基、硝基和基、呋喃基、被 1 至 3 个取代基取代的呋喃基,这些取代基选自卤素、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷氧基、三甲基、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷基亚磺酰基、具有 1 至 8 个碳原子的直链或支链烷基磺酰基、基、硝基和基、噻吩基、被 1 至 3 个从卤素中选出的取代基取代的噻吩基、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷氧基、三甲基、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷基亚磺酰基、具有 1 至 8 个碳原子的直链或支链烷基磺酰基、基、硝基和基、吡咯基、被 1 至 3 个选自卤素的取代基取代的吡咯基、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷氧基、三甲基、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷基亚磺酰基、具有 1 至 8 个碳原子的直链或支链烷基磺酰基、基、硝基和基、吡啶基或被 1 至 3 个取代基取代的吡啶基,取代基可从卤素、具有 1 至 8 个碳原子的直链或支链烷基、具有 1 至 8 个碳原子的直链或支链烷氧基中选出、三甲基、1 至 8 个碳原子的直链或支链烷基、1 至 8 个碳原子的直链或支链 烷基亚磺酰基、1 至 8 个碳原子的直链或支链烷基磺酰基、基、硝基和基:Y 指单键或具有 1 至 8 个碳原子的直链或支链亚烷基,链中可能有双键; W 指式(i)的基团 (其中 R³ 和 R⁴ 相同或不同,分别指氢或卤素,X 指 -O- 或 -S-,Z 指单键或 -O-,A 指具有 1 至 8 个碳原子的直链或支链亚烷基,B 指 -N(R⁸)(R⁹)(其中 R⁸ 和 R𠞙 相同或不同,分别指氢或具有 1 至 8 个碳原子的直链或支链烷基、或组合指与邻近的氮一起形成的基团、1-吡咯烷基、2-氧代-1-吡咯烷基、哌啶基、1-哌嗪基、在 4 位上被具有 1 至 8 个碳原子的直链或支链烷基取代的 1-哌嗪基、1-高哌嗪基、吗啉基和硫代吗啉基)或式 (ii) 的基团 (其中 R¹² 和 R¹³ 相同或不同,分别指氢或具有 1 至 8 个碳原子的直链或支链烷基、P 是-S-,Q 是六亚甲基、七亚甲基、八亚甲基、1-甲基五亚甲基、1-甲基六亚甲基、1-甲基七亚甲基、-(CH₂)₂S(CH₂)₃-、-(CH₂)₂S(CH₂)₆-。 或 其药学上可接受的盐或其合物。 这些化合物对原内酯肽酶具有抑制活性。还公开了含有新型吡啶化合物的药物组合物。
  • US5001137A
    申请人:——
    公开号:US5001137A
    公开(公告)日:1991-03-19
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