1-(2-isopropyl-5-methyl-cyclohexyloxy)-3-piperidin-1-yl-propanol

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 1-(2-isopropyl-5-methyl-cyclohexyloxy)-3-piperidin-1-yl-propanol
• 英文别名: 1-{[5-Methyl-2-(propan-2-yl)cyclohexyl]oxy}-3-(piperidin-1-yl)propan-2-ol；1-(5-methyl-2-propan-2-ylcyclohexyl)oxy-3-piperidin-1-ylpropan-2-ol
• 化学式: C₁₈H₃₅NO₂
• mdl: MFCD00691829
• 分子量: 297.481
• InChiKey: UGFKGDCZWPHAQX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  21
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  32.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  哌啶 、 2-[(2-异丙基-5-甲基-环己氧基)甲基]环氧乙烷 在 水 作用下， 反应 18.0h， 以55%的产率得到1-(2-isopropyl-5-methyl-cyclohexyloxy)-3-piperidin-1-yl-propanol
  参考文献：
  名称：

  [EN] ANALGESIC THAT BINDS FILAMIN A
  [FR] ANALGÉSIQUE QUI SE LIE À LA FILAMINE A

  摘要：

  公开了一种化合物、组合物及方法，能够提供镇痛效果。所考虑的化合物具有与式A相对应的结构，其中A、B、X、R1、R2、R7和R8以及虚线均在定义范围内。

  公开号：

  WO2010051374A1

文献信息

• [EN] A METHOD OF INHIBITING TAU PHOSPHORYLATION<br/>[FR] MÉTHODE POUR INHIBER LA PHOSPHORYLATION DE LA PROTÉINE TAU
  申请人：PAIN THERAPEUTICS INC

  公开号：WO2014011917A2

  公开（公告）日：2014-01-16

  A method of inhibiting phosphorylation of the tau protein and/or a TLR4-mediated immune response is disclosed. The method contemplates administering to cells in recognized need thereof such as cells of the central nervous system an effective amount of a of a compound or a pharmaceutically acceptable salt thereof that binds to a pentapeptide of filamin A (FLNA) of SEQ ID NO: 1, and contains at least four of the six pharmacophores of FIGS. 35-40.

  揭示了一种抑制tau蛋白的磷酸化和/或TLR4介导的免疫反应的方法。该方法考虑向认可需要的细胞，如中枢神经系统的细胞，施用有效量的结合到filamin A（FLNA）的五肽的化合物或其药用可接受的盐，该五肽的SEQ ID NO: 1，并且至少包含图35-40中的六个药效团中的四个。
• [EN] METHOD FOR INHIBITING GROWTH OF CANCER CELLS<br/>[FR] PROCÉDÉ POUR INHIBER LA CROISSANCE DE CELLULES CANCÉREUSES
  申请人：PAIN THERAPEUTICS INC

  公开号：WO2015054027A1

  公开（公告）日：2015-04-16

  1 A method of inhibiting the growth of cancer cells is disclosed in which cancer cells that contain an enhanced amount relative to non-cancerous cells of one or more of phosphorylated mTOR, Aktl, ERK2 and serine2152-phosphorylated filamin A are contacted with an FLNA-binding effective amount of a compound or a pharmaceutically acceptable salt thereof that binds to the pentapeptide of filamin A (FLNA) of SEQ ID NO: 1 and exhibits at least about 60 percent of the FITC- labeled naloxone binding amount when present at a 10 μΜ concentration and using unlabeled naloxone as the control inhibitor at the same concentration. A compound that binds to the FLNA pentapeptide preferably also contains at least four of the six pharmacophores of Figs. 19-24.

  本发明揭示了一种抑制癌细胞生长的方法，其中将相对于非癌细胞含有增强量的一个或多个磷酸化mTOR、Aktl、ERK2和丝氨酸2152-磷酸化filamin A的癌细胞与与filamin A（FLNA）的SEQ ID NO: 1的五肽结合并且在10μΜ浓度下至少表现出FITC标记的纳洛酮结合量的60％的化合物或其药学上可接受的盐接触。优选结合到FLNA五肽的化合物还包含Figs. 19-24中的六个药效团中的至少四个。
• ANALGESIC THAT BINDS FILAMIN A
  申请人：Burns Barbier Lindsay

  公开号：US20100279997A1

  公开（公告）日：2010-11-04

  A compound, composition and method are disclosed that can provide analgesia. A contemplated compound has a structure that corresponds to Formula A, wherein A, B, X, R 1 , R 2 , R 7 and R 8 , and the dashed lines are defined within.

  公开了一种可以提供镇痛作用的化合物、组合物和方法。考虑到的化合物具有与A公式相对应的结构，其中A、B、X、R1、R2、R7和R8以及虚线在其中定义。
• METHOD FOR INHIBITING GROWTH OF CANCER CELLS
  申请人：Pain Therapeutics, Inc.

  公开号：EP3791875A1

  公开（公告）日：2021-03-17

  A method of inhibiting the growth of cancer cells is disclosed in which cancer cells that contain an enhanced amount relative to non-cancerous cells of one or more of phosphorylated mTOR, Akt1, ERK2 and serine2152-phosphorylated filamin A are contacted with an FLNA-binding effective amount of a compound or a pharmaceutically acceptable salt thereof that binds to the pentapeptide of filamin A (FLNA) of SEQ ID NO: 1 and exhibits at least about 60 percent of the FITC-labeled naloxone binding amount when present at a 10 µM concentration and using unlabeled naloxone as the control inhibitor at the same concentration. A compound that binds to the FLNA pentapeptide preferably also contains at least four of the six pharmacophores of Figs. 19-24.

  本发明公开了一种抑制癌细胞生长的方法，该方法是将含有磷酸化的 mTOR、Akt1、ERK2 和丝氨酸 2152 磷酸化的丝胺 A 中的一种或多种含量相对于非癌细胞有所增加的癌细胞，与 FLNA 结合有效量的化合物或其药学上可接受的盐接触，该化合物或其药学上可接受的盐与 SEQ ID NO：1的五肽（FLNA）结合的化合物或其药学上可接受的盐，当其浓度为10 µM时，显示出至少约60%的FITC标记的纳洛酮结合量，并以相同浓度的未标记纳洛酮作为对照抑制剂。与 FLNA 五肽结合的化合物最好还含有图 19-24 中六种药效团中的至少四种。
• Method of inhibiting tau phosphorylation
  申请人：Wang Hoau-Yan

  公开号：US10017736B2

  公开（公告）日：2018-07-10

  A method of inhibiting phosphorylation of the tau protein and/or a TLR4-mediated immune response is disclosed. The method contemplates administering to cells in recognized need thereof such as cells of the central nervous system an effective amount of a of a compound or a pharmaceutically acceptable salt thereof that binds to a pentapeptide of filamin A (FLNA) of SEQ ID NO: 1, and contains at least four of the six pharmacophores of FIGS. 35-40.

  本发明公开了一种抑制 tau 蛋白磷酸化和/或 TLR4 介导的免疫反应的方法。该方法考虑向有公认需要的细胞如中枢神经系统细胞施用有效量的化合物或其药学上可接受的盐，该化合物或其药学上可接受的盐与 SEQ ID NO: 1 的丝胺 A (FLNA) 五肽结合，并包含图 35-40 六种药效团中的至少四种。