CAS: 36364-49-5; 1H-Imidazole 2-Hydroxybenzoate

该化合物是一种化学化合物,其独特结构将一非二氮环与硅酸盐溶性结合起来,其特点是其独特的结构,该化合物通常具有与其成分相关的特性,包括因其生物意义而闻名的氨氮酸盐结构可能具有的抗微生物和抗氟活动; 氨氨酸盐经常用于制药配方,特别是用于热门应用,因为它能够提高皮肤渗透和提供治疗效果; 该化合物一般在极地溶剂中溶解,便于将其纳入各种配方; 此外,该化合物还可能表现出依赖pH的溶性,使之适合于对pH的调节有益具体应用; 安全和处理预防措施,与许多化学物质一样,对于减轻与接触有关的任何潜在风险至关重要. 总的来说,氨酸盐酸盐是一种多用途化合物,在医药化学和药理学中应用,反映了其结构成分在影响其生物活动和溶液特性方面的重要性.

结构式图片

合成工艺路线路线简述

  • 合成目标产物 Imidazole 主要起始原料 Imidazole And Salicylic Acid
  • (文献来源)合成步骤主要原料 Imidazole 和 Salicylic Acid
📜咪唑,水杨酸 以 甲醇 用作溶剂,化学反应生成水杨酸咪唑
参考文献:不同极性溶剂中生物活性部分的二元 Ct 复合物共晶的设计,合成,表征和 Dft 计算,以研究其药理活性
标题:不同极性溶剂中生物活性部分的二元 Ct 复合物共晶的设计,合成,表征和 Dft 计算,以研究其药理活性
摘要:咪唑(im)和水杨酸(sa)在药用化合物中占有重要地位.这些被广泛用作抗真菌,抗菌,抗癌,免疫抑制剂等外用药物......
Doi:10.1080/07391102.2022.2158937

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专利信息


专利号:US-8546532-B2
优先权日:2008-04-17
标题:Synthesis of directed sequence polymer compositions and antibodies thereof for the treatment of protein conformational disorders
发明人:BONNIN DUSTAN; ZANELLI ERIC; MATHERS THOMAS
权利人:BONNIN DUSTAN; ZANELLI ERIC; MATHERS THOMAS; DECLION PHARMACEUTICALS INC
摘要:The instant invention comprises a process for the solid phase synthesis of directed epitope peptide mixtures useful in the treatment and diagnosis of protein conformational disorders, such process defined by a set of rules regarding the identity and the frequency of occurrence of amino acids that substitute a base or native amino acid of a known epitope. The resulting composition is a mixture of related peptides for therapeutic use. The invention also pertains to the process of generating antibodies using the directed epitope peptide mixtures as the antigens, and antibodies generated by such process, useful in the treatment and diagnostics of the said protein conformational disorder.

专利号:US-2024287041-A1
优先权日:2021-05-20
标题 :Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms
发明人:BALOGLU ERKAN; AUSTAD BRIAN C; ROE DAVID G; KEDUC ANDREW; GOTTSCHLING STEPHEN EDMUND; HECKER EVAN
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The present invention relates to a method of preparing a compound represented by structural formula (VII), comprising reacting a compound represented by structural formula (II), with a compound represented by structural formula (III), in a solvent, in the presence of a Pd catalyst and one or more inorganic bases under conditions suitable to prepare a compound represented by structural formula (VII): The values and example values of the variables in structural formulas (VII), (II), and (III) are defined herein. The present invention also relates to crystalline Forms I and II of the compound represented by Structural Formula (VII), the use of the crystalline Forms in treating disease or disorders associated with CRM1 and method of preparing the crystalline Forms.

专利号:AU-2022276509-A1
优先权日:2021-05-20
标题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

专利号:US-9994558-B2
优先权日:2013-09-20
标题 :Multicyclic compounds and methods of using same
发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to compounds represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders (e.g., PAK-mediated, for example, PAK4-mediated, diseases and disorders).

专利号:WO-2022246227-A1
优先权日:2021-05-20
标 题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

专利号:US-10363247-B2
优先权日:2015-08-18
标 题:(S,E)-3-(6-aminopyridin-3-yl)-N-((5-(4-(3-fluoro-3-methylpyrrolidine-1-carbonyl)phenyl-7-(4-fluorophenyl)benzofuran-2-yl)methyl)acrylamide for the treatment of cancer
发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to substituted benzofuranyl compounds and, more particularly, to a compound represented by Structural Formula 1a: (I) or a pharmaceutically acceptable salt thereof. The invention also includes the synthesis and use of the compound of Structural Formula 1a, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of diseases or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T-Cell mediated autoimmune disease) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.

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主要参考文献


1: Montrone F, Petrillo M, Ardizzone S, Scaricabarozzi I, Scotti A, Caruso I, Bianchi Porro G. Imidazole salicylate versus piroxicam in the treatment of arthrosis in elderly patients. A double-blind clinical and endoscopic trial. J Am Geriatr Soc. 1990 Sep;38(9):985-8.

合成参考文献


摘要:Arzneimittel-Forschung. Drug Research., 33(716), 1983 []
摘要:Lorenzano E, Badalamenti S, Scotti A, Scaricabarozzi I, Chinea B, Salerno F. Renal effects of imidazole-2-hydroxybenzoate in patients with compensated liver cirrhosis. Int J Clin Pharmacol Ther Toxicol. 1992 Jul;30(7):225–9.
参考文献:10.2165/00003495-199300461-00024
摘要:Bianco S, Robuschi M, Petrigni G, Scuri M, Pieroni MG, Refini RM, Vaghi A, Sestini PS. Efficacy and tolerability of nimesulide in asthmatic patients intolerant to aspirin. Drugs. 1993;46 Suppl 1():115–20. doi: 10.2165/00003495-199300461-00024.
参考文献:10.2165/00003495-199300461-00065
摘要:Ispano M, Fontana A, Scibilia J, Ortolani C. Oral challenge with alternative nonsteroidal antiinflammatory drugs (NSAIDs) and paracetamol in patients intolerant to these agents. Drugs. 1993;46 Suppl 1():253–6. doi: 10.2165/00003495-199300461-00065.
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