CAS: 65847-85-0; 2-Morpholinoethyl 2-((3-(Trifluoromethyl)Phenyl)Amino)Nicotinate

该化合物是一种化学化合物,被归类为非类固醇抗炎药物(NSAID),主要用于其止痛和抗炎特性,其特征是能够抑制环氧酶(COX)酶,这种酶在综合治疗各种炎症和疼痛中起着关键作用;治疗各种炎症和疼痛时经常使用创伤性创伤性痛苦;该化合物一般是口服的,并因其相对有利的安全性特征而闻名于其他非亚甲胺药物(NSID),其药用植物动因包括吸收,分配,代谢和排泄,这可以因个别病人因素而有所不同;还注意到,甲状腺阻因有可能提供治疗利益,降低胃肠侧效应的风险,这是与传统的非甲酸性痛苦症的共同关切;与任何药物一样,在开药或使用止痛剂时,必须考虑抗反反应,潜在的药物相互作用以及个别病人的反应.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号128699-18-3 2-chloronicotin... | CAS号98-16-8 间三氟甲苯胺

合成工艺路线路线简述

    📜2-Chloronicotinic Acid (2-Morpholinoethyl) Ester,间氨基三氟甲苯置于碘体系中,用 5,5-Dimethyl-1,3-Cyclohexadiene,二氯甲烷,异丙醇 作为反应溶剂,以35%的收率获得产物吗尼氟酯
    参考文献:Processes For The Preparation Of Morniflumate And Analogous Compounds
    标题:Processes For The Preparation Of Morniflumate And Analogous Compounds
    摘要:描述了用于制备莫尼氟酸和类似化合物的新型工艺,这些工艺能够直接获得产品的自由碱形式,采用简化的合成方案,并且产率显著高于先前工艺获得的产率.本发明的工艺对于工业应用尤为有利.

    海关参考信息

    专利信息


    专利号:US-9051302-B2
    优先权日:2008-01-15
    标 题 :Synthesis of resorcylic acid lactones useful as therapeutic agents
    发明人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN
    权利人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN; UNIV STRASBOURG
    摘要:Disclosed are macrocyclic compounds of formulae I, I′, II, II′, III, III′, IV, and V, which are analogs of the pochonin resorcylic acid lactones, pharmaceutical compositions comprising the compounds, and methods and uses comprising the compounds for the treatment of diseases mediated by kinases and Heat Shock Protein 90 HSP90.

    专利号:US-7504409-B2
    优先权日:2000-01-31
    标 题:Mucin synthesis inhibitors
    发明人:ZHOU YUHONG; LEVITT ROY C; NICOLAIDES NICHOLAS C; JONES STEVE; MCLANE MIKE
    权利人:GENAERA CORP
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases.

    专利号:US-2005249675-A1
    优先权日:2003-06-19
    标 题 :Mucin synthesis inhibitors
    发明人:HUNG HSIAO-LING; CHELLQUIST ERIC; LEVITT ROY C; MCLANE MICHAEL
    权利人:HUNG HSIAO-LING; CHELLQUIST ERIC; LEVITT ROY C; MCLANE MICHAEL
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases.

    专利号:US-7345051-B2
    优先权日:2000-01-31
    标题 :Mucin synthesis inhibitors
    发明人:ZHOU YUHONG; LEVITT ROY C; NICOLAIDES NICHOLAS C; JONES STEVE; MCLANE MIKE
    权利人:GENAERA CORP
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds of Formula II in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases. n nwhereinn X is S, N, O or CR; Y is CRR′, O, NR 6 , CRR′—CRR′ or CRâ•?CR; Z is NR 6 , O, S, CRR′ or CRR′—CRR′; R 1 -R 3 are independently selected from the group consisting of H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, amino, hydroxy, halosubstituted alky and halo; R 4 is n n n n n n n n n n n n n n n n n n n Q is CR, NR 6 or n n n n n n n n n n n n R 5 is H or benzyl; n R 6 is H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, OH or halo; and n R and R′ are independently H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, OH or halo,n nor a harmaceutically acceptable salt thereof.

    专利号:US-2002147216-A1
    优先权日:2000-01-31
    标 题:Mucin synthesis inhibitors
    发明人:ZHOU YUHONG; LEVITT ROY C; NICOLAIDES NICHOLAS C; JONES STEPHEN; MCLANE MIKE
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases.

    专利号:US-2002165244-A1
    优先权日:2000-01-31
    标 题 :Mucin synthesis inhibitors
    发明人:ZHOU YUHONG; LEVITT ROY C; NICOLAIDES NICHOLAS C; JONES STEVE; MCLANE MIKE
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Jeong SH, Jang JH, Lee YB. Modeling population pharmacokinetics of morniflumate in healthy Korean men: extending pharmacometrics analysis to niflumic acid, its major active metabolite. Naunyn Schmiedebergs Arch Pharmacol. 2024 Feb;397(2):843-856. doi: 10.1007/s00210-023-02640-0. Epub 2023 Jul 29. 113(5):853-863. doi: 10.23736/S0026-4806.22.08200-3. Epub 2022 Jun 14.
    610:121224. doi: 10.1016/j.ijpharm.2021.121224. Epub 2021 Oct 25. 16(8):3514-3523. doi: 10.1021/acs.molpharmaceut.9b00351. Epub 2019 Jul 18. 55(1):95-101. doi: 10.5414/CP202678. 43(3):290-302. doi: 10.1177/0300060514567212. Epub 2015 Apr 28. 27(11):1438-43. doi: 10.1002/bmc.2940. Epub 2013 May 30. 26(1):247-50. doi: 10.1177/039463201302600126. 53(8):812-3. doi: 10.1111/j.1398-9995.1998.tb03980.x. 2(5):494-5. French. doi: 10.1016/0929-693x(96)81190-0. 33(3-4):233-9. doi: 10.1007/BF01986568. 13(1-2):51-60. Italian. 12(6):347-57. Italian. 18(1):30-6. doi: 10.1177/030006059001800105. Erratum in: J Int Med Res 1990 Mar- Apr;18(2):preceding 75. 111(5):507-10. French. 68(10):507-13. Italian. 14(2):247-56. doi: 10.1007/BF01966649. 34(8):885-90.

    合成参考文献


    参考文献:10.2165/11532890-000000000-00000
    摘要:Leroy S, Marc E, Bavoux F, Tréluyer JM, Gendrel D, Bréart G, Pons G, Chalumeau M. Hospitalization for severe bacterial infections in children after exposure to NSAIDs: a prospective adverse drug reaction reporting study. Clin Drug Investig. 2010;30(3):179–85. doi: 10.2165/11532890-000000000-00000.
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