5-methyl-4-propan-2-yl-3,6-dihydro-2H-pyran

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡喃
• 英文名称: 5-methyl-4-propan-2-yl-3,6-dihydro-2H-pyran
• 化学式: C₉H₁₆O
• 分子量: 140.22
• InChiKey: GXGGFOPYTHCYBJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

文献信息

• [EN] CHROMANE, ISOCHROMANE AND DIHYDROISOBENZOFURAN DERIVATIVES AS mGluR2-NEGATIVE ALLOSTERIC MODULATORS, COMPOSITIONS, AND THEIR USE<br/>[FR] DÉRIVÉS DE CHROMANE, D'ISOCHROMANE ET DE DIHYDROISOBENZOFURANE EN TANT QUE MODULATEURS ALLOSTÉRIQUES NÉGATIFS DE MGLUR2, COMPOSITIONS ET LEUR UTILISATION
  申请人：MERCK SHARP & DOHME

  公开号：WO2018063955A1

  公开（公告）日：2018-04-05

  The present invention provides certain substituted chromane, isochromane, and dihydroisobenzofuran compounds of formula (I) or a pharmaceutically acceptable salt thereof, wherein ring A is a moiety selected from (II), (III), (IV), and (V), and ring B, n, R1, R2, R2A, R3, and R3A are as defined herein. The compounds of the invention are useful as mGluR2 inhibitors, or mGluR2 negative allosteric modulators (NAMs), and may be useful in methods of treating a patient for diseases or disorders in which the mGluR2-NAM receptor is involved, such as Alzheimer's disease, cognitive impairment, mild congnitive impairment, schizophrenia and other mood disorders, pain disorders and sleep disorders, by administering to the patient a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof. The invention is also directed to pharmaceutical compositions comprising a compound of the invention, or a pharmaceutically acceptable salt thereof, (optionally in combination with one or more additional active ingredients), and a pharmaceutically acceptable carrier, and the use of the compounds and pharmaceutical compositions of the invention in the treatment of such diseases.

  本发明提供了某些取代的色苷、异色苷和二氢异苯并呋喃化合物的化学结构（I），或其药学上可接受的盐，其中环A是从（II）、（III）、（IV）和（V）中选择的基团，环B、n、R1、R2、R2A、R3和R3A如本文所定义。本发明的化合物可用作mGluR2抑制剂，或mGluR2负向变构调节剂（NAMs），并可用于治疗mGluR2-NAM受体参与的疾病或障碍的方法，如阿尔茨海默病、认知障碍、轻度认知障碍、精神分裂症和其他情绪障碍、疼痛障碍和睡眠障碍，通过向患者投予本发明化合物或其药学上可接受的盐的治疗有效量。本发明还涉及含有本发明化合物或其药学上可接受的盐（可选地与一个或多个额外活性成分组合）和药学上可接受的载体的药物组合物，以及在治疗这些疾病中使用本发明的化合物和药物组合物。
• Modulators of KV3 channels to treat pain
  申请人：Autifony Therapeutics Limited

  公开号：US11147813B2

  公开（公告）日：2021-10-19

  The present invention provides a modulator of Kv3.1 and/or Kv3.2 and/or Kv3.3 channels for use in the prophylaxis or treatment of pain. Modulators for use in the prophylaxis or treatment of pain include compounds of formula (I) or a pharmaceutically acceptable salt and/or solvate thereof and/or derivative thereof: (I).

  本发明提供了一种用于预防或治疗疼痛的 Kv3.1 和/或 Kv3.2 和/或 Kv3.3 通道调节剂。用于预防或治疗疼痛的调节剂包括式(I)化合物或其药学上可接受的盐和/或溶液和/或其衍生物：(I).
• HYDANTOIN MODULATORS OF KV3 CHANNELS
  申请人：Autifony Therapeutics Limited

  公开号：EP3390394B1

  公开（公告）日：2022-05-25
• 4, 5-RING ANNULATED INDOLE DERIVATIVES FOR TREATING OR PREVENTING OF HCV AND RELATED VIRAL INFECTIONS
  申请人：Anilkumar Gopinadhan N.

  公开号：US20100196319A1

  公开（公告）日：2010-08-05

  The present invention relates to 4,5-ring annulated indole derivatives of formula (I), compositions comprising at least one 4,5-ring annulated indole derivatives, and methods of using the 4,5-ring annulated indole derivatives for treating or preventing a viral infection or a virus-related disorder in a patient, wherein ring Z of formula (I), is cyclohexyl, cyclohexenyl, 6-membered heterocycloalkyl, 6-membered heterocycloalkenyl, 6-membered aryl or 6-membered heteroaryl, wherein R 1 , R 2 , R 3 , R 6 , R 7 and R 10 are as described herein.
• [EN] 4, 5-RING ANNULATED INDOLE DERIVATIVES FOR TREATING OR PREVENTING OF HCV AND RELATED VIRAL INFECTIONS<br/>[FR] DÉRIVÉS CONDENSÉS À 4,5 NOYAUX DESTINÉS AU TRAITEMENT OU À LA PRÉVENTION DU VHC ET DES INFECTIONS VIRALES ASSOCIÉES
  申请人：SCHERING CORP

  公开号：WO2008082488A1

  公开（公告）日：2008-07-10

  [EN] The present invention relates to 4, 5 - ring annulated indole derivatives of formula ( I ), compositions comprising at leas t one 4, 5 - ring annulated indole derivatives, and methods of using the 4, 5 - ring annulated ^ndole derivatives for treating or preventing a viral inf ection or a virus - related disorder in a patient, (I) wherein ring Z of formula (I), is cyclohexyl, cyclohexenyl, 6-membered heterocycloalkyl, 6- membered heterocycloalkenyl, 6-membered aryl or 6-membered heteroaryl, wherein R¹, R², R³, R⁶. R⁷ and R¹⁰ are as described herein.
  [FR] L'invention concerne des dérivés indole condensés à 4,5 noyaux de la formule (I), des compositions renfermant au moins un dérivé indole condensé à 4,5 noyaux, et des procédés d'utilisation des dérivés indole condensés à 4,5 noyaux dans le traitement ou la prévention d'une infection virale ou d'un trouble lié à un virus chez un patient, (I) le cycle Z de la formule (I) étant cyclohexyle, cyclohexényle, hétérocycloalkyle à 6 chaînons, hétérocycloalcényle à 6 chaînons, aryle à 6 chaînons ou hétéroaryle à 6 chaînons, où R¹, R², R³, R⁶, R⁷ et R¹⁰ sont tels que définis dans la description.