2-Hydroxy-4-methoxybenzaldehyde, butyl ether | 938117-51-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-Hydroxy-4-methoxybenzaldehyde, butyl ether
• 英文别名: 2-butoxy-4-methoxybenzaldehyde
• CAS: 938117-51-2
• 化学式: C₁₂H₁₆O₃
• 分子量: 208.257
• InChiKey: VFKFKKNOQRIWLE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-Hydroxy-4-methoxybenzaldehyde, butyl ether 在 sodium methylate 作用下， 以 四氢呋喃 、 甲醇 、 5,5-dimethyl-1,3-cyclohexadiene 为溶剂， 反应 6.0h， 生成 methyl 4-butoxy-6-methoxy-1H-indole-2-carboxylate
  参考文献：
  名称：

  Design, synthesis and antiproliferative activity of a novel class of indole-2-carboxylate derivatives

  摘要：

  Based on the chemical structure of Pyrroloquinoline quinone (PQQ), a novel class of indole-2-carboxylate derivatives was designed, synthesized and assayed for antiproliferative activity in cancer cells in vitro. The biological results showed that some derivatives exhibited significant antiproliferative activity against HepG2, A549 and MCF7 cells. Notably, the novel compounds, methyl 6-amino-4-cyclohexylmethoxy-1H-indole-2-carboxylate (6e) and methyl 4-isopropoxy-6-methoxy-1H-indole-2-carboxylate (9l) exhibited more potent antiproliferative activity than the reference drugs PQQ and etoposide in vitro, with IC50 values ranging from 3.78 ± 0.58 to 24.08 ± 1.76 μM. Further biological assay showed that both compounds 6e and 9l increased ROS generation dose-dependently, and induced PARP cleavage in A549 cells. Consequently, 6e and 9l appeared as promising anticancer lead compounds for further optimization.

  DOI：

  10.1016/j.ejmech.2014.05.043

文献信息

• [EN] N-SUBSTITUTED PIPERIDINE DERIVATIVES AS SEROTONIN RECEPTOR AGENTS<br/>[FR] DÉRIVÉS DE PIPÉRIDINE N-SUBSTITUÉS EN TANT QU'AGENTS SPÉCIFIQUES DES RÉCEPTEURS DE LA SÉROTONINE
  申请人：ACADIA PHARM INC

  公开号：WO2010111353A1

  公开（公告）日：2010-09-30

  Disclosed herein are substantially pure forms of the compounds of Formula (I), (II), (III), (IV) and (V), or a pharmaceutically acceptable salt, prodrug, hydrate, solvate, polymorph, stereoisomer or ester thereof. Also disclosed are methods of inhibiting an activity of a serotonin receptor, methods inhibiting an activation of a serotonin receptor, and methods of alleviating or treating various disease conditions and side effects.

  本发明公开了公式(I)、(II)、(III)、(IV)和(V)的化合物的几乎纯净形式，或其药物可接受的盐、前药、水合物、溶剂化物、多态、对映异构体或酯。还公开了抑制血清素受体活性的方法、抑制血清素受体激活的方法，以及缓解或治疗各种疾病状况和副作用的方法。
• Hydroxy-Substituted Diphenylazetidinones for the Treatment of Hyperlipidemia
  申请人：JAEHNE Gerhard

  公开号：US20080274947A1

  公开（公告）日：2008-11-06

  The present invention comprises compounds and compositions for the treatment of metabolic disorders and more particularly, those insulin-related metabolic disorders of the blood such as hyperlipidemia, diabetes, insulin-resistance and the like comprising diphenylazetidinones compounds which have an additional hydroxy function in the 2″ position and their salts. The invention therefore relates to compounds of formula I: in which the meanings R1, R2, R3, R4, R5, R6 are defined herein.

  本发明涉及用于治疗代谢紊乱的化合物和组合物，更具体地说，是血液中的胰岛素相关代谢紊乱，如高脂血症、糖尿病、胰岛素抵抗等，包括二苯基氮杂环丁酮化合物，其在2″位置具有额外的羟基功能及其盐。因此，本发明涉及公式I的化合物：其中R1、R2、R3、R4、R5、R6的含义在此定义。
• DIPHENYLHETEROCYCLE CHOLESTEROL ABSORPTION INHIBITORS
  申请人：Talley John

  公开号：US20090186834A1

  公开（公告）日：2009-07-23

  Various azetidinone, pyrrolidine, imidazolidine, and oxazolidine derivatives are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.

  本文描述了各种吡咯烷、咪唑啉和噁唑烷衍生物，以及含有这些化合物的药物组合物和使用这些化合物治疗疾病的方法。还描述了其他实施方式。
• [DE] HYDROXY-SUBSTITUIERTE DIPHENYLAZETIDINONE ZUR BEHANDLUNG VON HYPERLIPIDÄMIE<br/>[EN] HYDROXY-SUBSTITUTED DIPHENYLAZETIDINONES FOR THE TREATMENT OF HYPERLIPIDAEMIA<br/>[FR] DIPHENYLAZETIDINONE HYDROXY-SUBSTITUEE UTILISEE DANS LE TRAITEMENT DE L'HYPERLIPIDEMIE
  申请人：SANOFI AVENTIS DEUTSCHLAND

  公开号：WO2007059871A1

  公开（公告）日：2007-05-31

  [EN] The invention relates to compounds of the formula (I) in which R1, R2, R3, R4, R5 and R6 are defined as specified, and to their physiologically compatible salts. The compounds are suitable, for example, as hypolipidaemic drugs.
  [FR] L'invention concerne des composés de formule (I), dans laquelle R1, R2, R3, R4, R5 et R6 sont spécifiées dans la description, ainsi que leurs sels physiologiquement acceptables. Les composés s'utilisent par exemple en tant qu'agents hypolipidémiques.
  [DE] Die Erfindung betrifft Verbindungen der Formel (I), worin R1, R2, R3, R4, R5, und R6 die angegebenen Bedeutungen haben, sowie deren physiologisch verträgliche Salze. Die Verbindungen eignen sich z.B. als Hypolipidämika.
• Design, synthesis and antiproliferative activity of a novel class of indole-2-carboxylate derivatives
  作者：Xing-yue Ji、Si-tu Xue、Yue-chen Zhan、Jia-jia Shen、Lin-tao Wu、Jie Jin、Zhen Wang、Zhuo-rong Li

  DOI：10.1016/j.ejmech.2014.05.043

  日期：2014.8

  Based on the chemical structure of Pyrroloquinoline quinone (PQQ), a novel class of indole-2-carboxylate derivatives was designed, synthesized and assayed for antiproliferative activity in cancer cells in vitro. The biological results showed that some derivatives exhibited significant antiproliferative activity against HepG2, A549 and MCF7 cells. Notably, the novel compounds, methyl 6-amino-4-cyclohexylmethoxy-1H-indole-2-carboxylate (6e) and methyl 4-isopropoxy-6-methoxy-1H-indole-2-carboxylate (9l) exhibited more potent antiproliferative activity than the reference drugs PQQ and etoposide in vitro, with IC50 values ranging from 3.78 ± 0.58 to 24.08 ± 1.76 μM. Further biological assay showed that both compounds 6e and 9l increased ROS generation dose-dependently, and induced PARP cleavage in A549 cells. Consequently, 6e and 9l appeared as promising anticancer lead compounds for further optimization.