(S)-methyl 3-(hydroxymethyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate | 1374671-74-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并二恶烷
• 英文名称: (S)-methyl 3-(hydroxymethyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate
• 英文别名: methyl (3S)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxine-6-carboxylate
• CAS: 1374671-74-5
• 化学式: C₁₁H₁₂O₅
• 分子量: 224.213
• InChiKey: ALWXOQUWKQAEEX-QMMMGPOBSA-N

物化性质

• 沸点：
  362.7±30.0 °C(Predicted)
• 密度：
  1.282±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (S)-methyl 3-(hydroxymethyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate 在 sodium hydride 、 一水合肼 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 96.0h， 生成 (S)-5-(3-(methoxymethyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1,3,4-oxadiazole-2-thiol
  参考文献：
  名称：

  Identification of Glycogen Synthase Kinase-3 Inhibitors with a Selective Sting for Glycogen Synthase Kinase-3α

  摘要：

  The glycogen synthase kinase-3 (GSK-3) has been linked to the pathogenesis of colorectal cancer, diabetes, cardiovascular disease, acute myeloid leukemia (AML), and Alzheimer's disease (AD). The debate on the respective contributions of GSK-3 alpha and GSK-3 beta to AD pathology and AML is ongoing. Thus, the identification of potent GSK-3 alpha-selective inhibitors, endowed with favorable pharmacokinetic properties, may elucidate the effect of GSK-3 alpha inhibition in AD and AML models. The analysis of all available crystallized GSK-3 structures provided a simplified scheme of the relevant hot spots responsible for ligand binding and potency. This resulted in the identification of novel scorpion shaped GSK-3 inhibitors. It is noteworthy, compounds 14d and 15b showed the highest GSK-3 alpha selectivity reported so far. In addition, compound 14d did not display significant inhibition of 48 out of 50 kinases in the test panel. The GSK-3 inhibitors were further profiled for efficacy and toxicity in the wild-type (wt) zebrafish embryo assay.

  DOI：

  10.1021/jm300309a
• 作为产物：
  描述：

  原儿茶酸 在 氯化亚砜 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 生成 (S)-methyl 3-(hydroxymethyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate
  参考文献：
  名称：

  Identification of Glycogen Synthase Kinase-3 Inhibitors with a Selective Sting for Glycogen Synthase Kinase-3α

  摘要：

  The glycogen synthase kinase-3 (GSK-3) has been linked to the pathogenesis of colorectal cancer, diabetes, cardiovascular disease, acute myeloid leukemia (AML), and Alzheimer's disease (AD). The debate on the respective contributions of GSK-3 alpha and GSK-3 beta to AD pathology and AML is ongoing. Thus, the identification of potent GSK-3 alpha-selective inhibitors, endowed with favorable pharmacokinetic properties, may elucidate the effect of GSK-3 alpha inhibition in AD and AML models. The analysis of all available crystallized GSK-3 structures provided a simplified scheme of the relevant hot spots responsible for ligand binding and potency. This resulted in the identification of novel scorpion shaped GSK-3 inhibitors. It is noteworthy, compounds 14d and 15b showed the highest GSK-3 alpha selectivity reported so far. In addition, compound 14d did not display significant inhibition of 48 out of 50 kinases in the test panel. The GSK-3 inhibitors were further profiled for efficacy and toxicity in the wild-type (wt) zebrafish embryo assay.

  DOI：

  10.1021/jm300309a

文献信息

• NOVEL BENZODIOXANE-PIPERIDINE DERIVATIVES AND THEIR THERAPEUTIC APPLICATIONS FOR TREATING NEUROPSYCHIATRIC DISORDERS
  申请人：PIERRE FABRE MEDICAMENT

  公开号：US20150336943A1

  公开（公告）日：2015-11-26

  The present invention concerns benzodioxane-piperidine with general formula I: wherein notably: R1 represents one or more identical or different substituent(s) on the benzene ring, each independently representing a hydrogen or halogen atom, or a C 1-4 alkyl group, or a C 1-4 alkoxy group or a C 1-4 hydroxyalkyl group or a C 1-4 alkylcarbonyl or an alkoxycarbonyl group or an OH group or an SO2R group with R alkyl, or a CN group, or a CF3 group, or an OCF 3 group; n=1, 2 or 3; m=0 or 1, and R2 represents one or more identical or different substituent(s) on the oxazolidinone or morpholinone ring, each independently representing: a hydrogen atom, a C 1-4 alkyl group, or a C 1-4 alkoxy group, or a C 1-4 hydroxyalkyl group, or an alkylcarbonyl group, or an alkoxycarbonyl group, or an alkoxyphenyl group.

  本发明涉及具有通式I的苯二氧杂环戊二酮： 其中特别地： R1代表苯环上一个或多个相同或不同的取代基，每个独立地代表氢或卤素原子，或C1-4烷基，或C1-4烷氧基，或C1-4羟基烷基，或C1-4烷基羰基，或烷氧羰基，或OH基，或SO2R基，其中R是烷基，或CN基，或CF3基，或OCF3基； n=1, 2或3； m=0或1，以及 R2代表噁唑烷酮或吗啉酮环上一个或多个相同或不同的取代基，每个独立地代表： 氢原子，C1-4烷基，或C1-4烷氧基，或C1-4羟基烷基，或烷基羰基，或烷氧羰基，或烷氧基苯基。
• NOUVEAUX DERIVES BENZODIOXANE-PIPERIDINE ET LEURS APPLICATIONS THERAPEUTIQUES POUR LE TRAITEMENT DES AFFECTIONS NEUROPSYCHIATRIQUES
  申请人：Pierre Fabre Médicament

  公开号：EP2941427A1

  公开（公告）日：2015-11-11
• NOUVEAUX DÉRIVÉS BENZODIOXANE-PIPERIDINE ET LEURS APPLICATIONS THÉRAPEUTIQUES POUR LE TRAITEMENT DES AFFECTIONS NEUROPSYCHIATRIQUES
  申请人：Pierre Fabre Médicament

  公开号：EP2941427B1

  公开（公告）日：2016-11-09
• [EN] NOVEL BENZODIOXANE-PIPERIDINE DERIVATIVES AND THERAPEUTIC USES THEREOF FOR THE TREATMENT OF NEUROPSYCHIATRIC DISORDERS<br/>[FR] NOUVEAUX DERIVES BENZODIOXANE-PIPERIDINE ET LEURS APPLICATIONS THERAPEUTIQUES POUR LE TRAITEMENT DES AFFECTIONS NEUROPSYCHIATRIQUES
  申请人：PF MEDICAMENT

  公开号：WO2014106660A1

  公开（公告）日：2014-07-10

  La présente invention concerne des dérivés benzodioxane-pipéridinerépondant à la formule générale I: dans laquelle notamment: -R1 représente un ou plusieurs substituant(s) identique(s) ou différent(s) sur le noyau benzénique, chacun représentant indépendamment un atome d'hydrogène ou un halogène, ou un groupe alkyle en C1-4, ou un groupe alkoxy en C1-4,ou un groupe hydroxyalkyle en C1-4, ou un groupe alkylcarbonyle, ou un groupe alkoxycarbonyle, ou un groupe OH, ou un groupe SO2R avec R alkyle, ou un groupe CN, ou un groupe CF3, ou un groupe OCF3,-n = 1, 2 ou 3; -m = 0 ou 1, et -R2 représente un ou plusieurs substituant(s) identique(s) ou différent(s) sur les noyaux oxazolidinone ou morpholinone, chacun représentant indépendamment: un atome d'hydrogène, ou un groupe alkyle en C1-4, ou un groupe alkoxy en C1-4, ou un groupe hydroxyalkyle en C1-4,ou un groupe alkylcarbonyle, ou un groupe alkoxycarbonyle,ou un groupe alkoxyphenyl.
• Identification of Glycogen Synthase Kinase-3 Inhibitors with a Selective Sting for Glycogen Synthase Kinase-3α
  作者：Fabio Lo Monte、Thomas Kramer、Jiamin Gu、Upendra Rao Anumala、Luciana Marinelli、Valeria La Pietra、Ettore Novellino、Bénédicte Franco、David Demedts、Fred Van Leuven、Ana Fuertes、Juan Manuel Dominguez、Batya Plotkin、Hagit Eldar-Finkelman、Boris Schmidt

  DOI：10.1021/jm300309a

  日期：2012.5.10

  The glycogen synthase kinase-3 (GSK-3) has been linked to the pathogenesis of colorectal cancer, diabetes, cardiovascular disease, acute myeloid leukemia (AML), and Alzheimer's disease (AD). The debate on the respective contributions of GSK-3 alpha and GSK-3 beta to AD pathology and AML is ongoing. Thus, the identification of potent GSK-3 alpha-selective inhibitors, endowed with favorable pharmacokinetic properties, may elucidate the effect of GSK-3 alpha inhibition in AD and AML models. The analysis of all available crystallized GSK-3 structures provided a simplified scheme of the relevant hot spots responsible for ligand binding and potency. This resulted in the identification of novel scorpion shaped GSK-3 inhibitors. It is noteworthy, compounds 14d and 15b showed the highest GSK-3 alpha selectivity reported so far. In addition, compound 14d did not display significant inhibition of 48 out of 50 kinases in the test panel. The GSK-3 inhibitors were further profiled for efficacy and toxicity in the wild-type (wt) zebrafish embryo assay.