CAS: 40107-93-5; 6,7-Dihydro-5H-Pyrrolo[3,4-B]Pyridin-5-One

该化合物是一种环环有机化合物,其特点是有引信的双环结构,包括一个火花和环.该化合物在的5处,具有碳基组,有助于其再活性和潜在的生物活动.该化合物一般在室温下是固体,在极地有机溶剂中可能表现出中等溶解性.氮原子在其结构中的存在可产生基本特性,使其得以参与各种化学反应,例如核细胞替代或与金属离子的协调.该化合物对医药化学具有兴趣,因为它具有潜在的药用特性,包括抗微生物和抗癌活动.其独特的结构特征使它成为开发新型治疗剂的宝贵树脂.与许多外循环一样,6,7-二氢苯丙烯-5one[3,4-b]的具体再活性和相互作用可能受到亚基成分和周围化学环境的影响.

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1256806-34-4 1256811-82-1 1211589-13-7

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CAS号89-00-9 吡啶-2,3-二羧酸 | CAS号4664-00-0 2,3-吡啶二甲酰亚胺

合成工艺路线路线简述

    📜2,3-吡啶二酰亚胺置于sodium Tetrahydroborate,溶剂黄146,锌体系中,用 甲醇,氯仿 作为反应溶剂,化学反应 6.0H,反应生成 6,7-二氢吡咯[3,4-B]并吡啶-5-酮
    参考文献:新型的人工氢化物辅助氟化辅因子的氧化还原生物催化荧光传感评估新方法
    标题:新型的人工氢化物辅助氟化辅因子的氧化还原生物催化荧光传感评估新方法
    摘要:开发了新的人工氟辅因子以替代天然辅因子nad(p),具有较高的氢化物转移能力.更重要的是,我们为评估建立了一种新的快速筛选方法.
    DOI:10.1039/c6Cc02002J

    海关参考信息

    专利信息


    专利号:US-9586964-B2
    优先权日:2011-10-28
    标 题:Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; HOPKINS COREY R; MELANCON BRUCE J; POSLUSNEY MICHAEL S; ENGERS DARREN W
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-8536164-B2
    优先权日:2010-12-20
    标 题:Fused pyridine compounds as casein kinase inhibitors
    发明人:BUTLER TODD W; CHANDRASEKARAN RAMALAKSHMI Y; MENTE SCOT R; SUBRAMANYAM CHAKRAPANI; WAGER TRAVIS T
    权利人:BUTLER TODD W; CHANDRASEKARAN RAMALAKSHMI Y; MENTE SCOT R; SUBRAMANYAM CHAKRAPANI; WAGER TRAVIS T; PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I: n nand pharmaceutically acceptable salts thereof, wherein X, Y, A, R 4 , n, and R 7 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1016/j.ejmech.2012.07.001
    摘要:Galli U, Mesenzani O, Coppo C, Sorba G, Canonico PL, Tron GC, Genazzani AA. Identification of a sirtuin 3 inhibitor that displays selectivity over sirtuin 1 and 2. European Journal of Medicinal Chemistry. 2012 Sep;55():58–66. doi: 10.1016/j.ejmech.2012.07.001.
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