摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

morpholine-4-carboxylic acid methyl-[4-(octahydro-quinoline-1-carbonyl)-benzyl]-amide | 936019-23-7

中文名称
——
中文别名
——
英文名称
morpholine-4-carboxylic acid methyl-[4-(octahydro-quinoline-1-carbonyl)-benzyl]-amide
英文别名
N-[[4-(3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carbonyl)phenyl]methyl]-N-methylmorpholine-4-carboxamide
morpholine-4-carboxylic acid methyl-[4-(octahydro-quinoline-1-carbonyl)-benzyl]-amide化学式
CAS
936019-23-7
化学式
C23H33N3O3
mdl
——
分子量
399.533
InChiKey
PKFKEHZNYHOCNI-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):
    2.5
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    53.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • PHARMACEUTICAL USE OF SUBSTITUTED AMIDES
    申请人:Andersen Henrik Sune
    公开号:US20090124598A1
    公开(公告)日:2009-05-14
    The use of substituted amides for modulating the activity of 11β-hydroxysteroid dehydrogenase type 1 (11βHSD1) and the use of these compounds as pharmaceutical compositions, are described. Also a novel class of substituted amides, their use in therapy, pharmaceutical compositions comprising the compounds, as well as their use in the manufacture of medicaments are described. The present compounds are modulators and more specifically inhibitors of the activity of 11βHSD1 and may be useful in the treatment of a range of medical disorders where a decreased intracellular concentration of active glucocorticoid is desirable.
    描述了使用替代酰胺来调节11β-羟基类固醇脱氢酶1(11βHSD1)活性以及将这些化合物用作药物组合物的用途。还描述了一类新型的替代酰胺,它们在治疗中的应用,包含这些化合物的药物组合物,以及它们在制造药物中的应用。目前的化合物是11βHSD1活性的调节剂,更具体地是抑制剂,并且可能在治疗一系列医学疾病中有用,其中降低细胞内活性糖皮质激素浓度是可取的。
  • [EN] PHARMACEUTICAL USE OF SUBSTITUTED AMIDES<br/>[FR] UTILISATION PHARMACEUTIQUE D'AMIDES SUBSTITUES
    申请人:NOVO NORDISK AS
    公开号:WO2007051810A2
    公开(公告)日:2007-05-10
    [EN] The use of substituted amides for modulating the activity of 11ß-hydroxysteroid dehydrogenase type 1 (11ßHSD1) and the use of these compounds as pharmaceutical compositions, are described. Also a novel class of substituted amides, their use in therapy, pharmaceutical compositions comprising the compounds, as well as their use in the manufacture of medicaments are described. The present compounds are modulators and more specifically inhibitors of the activity of 11ßHSD1 and may be useful in the treatment of a range of medical disorders where a decreased intracellular concentration of active glucocorticoid is desirable.
    [FR] La présente invention concerne l'utilisation d'amides substitués pour moduler l'activité de la 11ß-hydroxystéroïde deshydrogénase de type 1 (11ßHSD1) et l'utilisation de ces composés en tant que compositions pharmaceutiques. Cette invention concerne également une nouvelle classe d'amides substitués, leur utilisation à des fins thérapeutiques, des compositions pharmaceutiques comprenant des composés, ainsi que leur utilisation dans la fabrication de médicaments. Les composés décrits dans cette invention sont des modulateurs et plus spécifiquement des inhibiteurs de l'activité de la 11ßHSD1 et ils peuvent être utilisés pour traiter un éventail de pathologies pour lesquelles une concentration intracellulaire réduite de glucocorticoïde actif est souhaitable.
查看更多

同类化合物

锯齿石松宁 脱氧卡色素B 箭毒蛙毒素 C 环戊二烯并[b]吖庚英-5-醇,十氢- 坎库碘铵 十氢喹啉 十氢-2-甲基喹啉 八氢对苯二酚-4(1H)-酮 八氢喹啉-2(1H)-酮 八氢-2,6-喹啉二酮 二氯化硅2,3-萘醛菁 β-羟基丙基-环糊精 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-二甲基-1,2,3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十六氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-1,10a,12a-三甲基-2-氧代-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 8H-13,3,6a-乙基亚基-7,10-亚甲基噁庚并[3,4-i]-1-苯并吖辛因-8-酮,1-乙基十四氢-12a-羟基-6-甲氧基-3-甲基-,(3R,6S,6aS,7R,7aS,10S,12aS,13S,13aR,15R)-(9CI) 8-羟基-十氢喹啉 4-乙炔基-2-甲基十氢喹啉-4-醇 4-乙炔基-2-甲基-1-(3-苯丙-2-炔-1-基)十氢喹啉-4-醇 3-羟基-13,17-开环-5-雄甾烯-17-酸-13,17-内酰胺(4-(二(2-氯乙基)氨基)苯基)丁酸酯 3-甲氧基-17-氮杂-高雄甾-5-烯-17-酮 2H-环戊二烯并[b]吡啶-2-酮,八氢-4-甲基-,[4S-(4-α-,4a-bta-,7a-bta-)]-(9CI) 2-甲基-1-(3-丙氧基-丙基)-八氢-喹啉-4-酮 2,5-二丙基十氢喹啉 1-(3-甲氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1-(3-氯-丙基)-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1,2,2-三甲基-八氢-喹啉-4-酮 (4aS,4bR,8S,10aR,10bS,12aS)-10a,12a-二甲基-2-羰基-1,2,3,4,4a,4b,5,7,8,9,10,10a,10b,11,12,12a-十六氢萘并[2,1-f]喹啉-8-基{4-[二(2-氯乙基)氨基]苯基}乙酸酯 (4aS,4bR,6aS,8S,10aS,10bS,12aS)-8-羟基-10a,12a-二甲基-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢-1H-萘并[2,1-f]喹啉-2-酮 (3S,13R)-1,2,3,4,4aalpha,5,11,11aalpha-八氢-2,2,5-三甲基-3beta,5beta-乙桥-10bH-吡啶并[3,2-b]咔唑-10bbeta,13-二醇 (3R,6S,6aS,7R,7aS,10S,12aS,13R,13aR,14S,15R)-1-乙基十四氢-12a,14-二羟基-6-甲氧基-3-甲基-8H-13,3,6a-亚乙基-7,10-甲桥氧杂卓并[3,4-i]-1-苯并氮杂环辛四烯-8-酮 (2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮 (2R,4R,4As,8As)-rel-4-乙炔基十氢-1,2-二甲基-4-喹啉醇 1-(2-Cyclopentylethyl)-perhydrochinolin Perhydrodibenzochinolizin octahydroquinoline-1(2H)-carbonitrile N-Acetylbaikeidin 4-[4-[(4aR,8aR)-3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carbonyl]thiophen-2-yl]piperidine-1-carboxamide N-Chlor-trans-decahydrochinolin (4aR,8aR)-1-{4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidin-1-yl}-ethanone (7-Acetyl-3a,6-dimethyl-3-oxo-tetradecahydro-7-aza-cyclohepta[e]inden-6-yl)-acetic acid 6,7-Cyclobutano-1,2-cyclopropano-chinolizidin 2-Methyl-2,3-tetramethylen-N-cyanoaziridin (4aR)-2-oxo-1-[(1R)-1-phenylethyl]-4,5,6,7-tetrahydro-3H-quinoline-4a-carboxylic acid (4aR,8aR)-(octahydro-quinolin-1(2H)-yl)-(5-piperidin-4-yl-thiophen-3-yl)-methanone 5-(octahydroquinolin-1-yl)-5-oxopentanoic acid N-benzyl-N-isopropylamide 3,4,4-Trimethyl-2-azabicyclo<3.3.0>octan (4aR,8aR)-4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidine-1-carboxylic acid tert-butyl ester 1-Aza-4,11-dioxo-3-oxo-methoxycarbonyl-tricyclo<5.3.1.05,10>undecan