CAS: 30544-47-9; 2-(2-Hydroxyethoxy)Ethyl 2-((3-(Trifluoromethyl)Phenyl)Amino)Benzoate

该化合物是一种非类固醇抗炎药物,属于胎儿类,通常用作热门止痛剂和抗炎剂,其主要行动机制是抑制环氧酶(COX)酶,减少丙烯酸酯合成,从而减轻疼痛和炎症.Etofenamatate表现出有利的皮肤渗透性,使其对骨骼肌肉条件(如螺旋,菌株和关节炎)的局部治疗有效.其亲血性能可以提高组织渗透性,确保有针对性地交付.该化合物以其迅速开始行动并持续有效而闻名,在热液配方中具有牢固的安全性特征.Eteenamond往往倾向于在减轻疼痛和减少炎症症方面采取双重行动.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

2-(3-Trifluoromethyl-phenylamino)-benzoic acid 2-(2-benzyloxy-ethoxy)-ethyl ester 43H40F6N2O8C43H40F6N2O8 2-(2-Chloroethoxy)ethanol

合成工艺路线路线简述

    7-Phenyl-3,6,8,11-Tetraoxatridecane-1,13-Diyl Bis(2-((3-(Trifluoromethyl)Phenyl)Amino)Benzoate)置于palladium On Activated Charcoal 氢气体系中,用 甲醇 作为反应溶剂,化学反应生成 依托芬那酯
    参考文献:Boltze; Kreisfeld,Arzneimittel-Forschung/drug Research,1977,Vol. 27,# 6 B,P. 1300-1312
    标题:Boltze; Kreisfeld,Arzneimittel-Forschung/drug Research,1977,Vol. 27,# 6 B,P. 1300-1312

    海关参考信息

    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-2008280855-A1
    优先权日:2005-06-22
    标 题 :Process For the Production of Intermediates For the Preparation of Tricyclic Benzimidazoles
    发明人:CHIESA MARIA VITTORIA; PALMER ANDREAS; BUHR WILM; ZIMMERMANN PETER JAN; BREHM CHRISTOF; SIMON WOLFGANG-ALEXANDER; POSTIUS STEFAN; KROMER WOLFGANG; ZANOTTI-GEROSA ANTONIO
    权利人:NYCOMED GMBH
    摘要:The invention relates to a process for the synthesis of compounds of the formula 1-a and compounds of the formula 1-b. n n n n n n n n n n The compounds of the formula 1-a and the compounds of the formula 1-b, in which the substituents R1, R2, R3, and Ar have the meanings indicated in the description, are valuable intermediates for the preparation of pharmaceutically active compounds.

    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-2013035307-A1
    优先权日:2010-01-26
    标 题:Methods for treating or preventing the spread of cancer using semi-synthetic glycosaminoglycosan ethers
    发明人:PRESTWICH GLENN D; KENNEDY THOMAS P
    权利人:UNIV UTAH RES FOUND; PRESTWICH GLENN D; KENNEDY THOMAS P
    摘要:Described herein are methods for the treatment and prevention of tumor metastasis using alkylated and fluoroalkylated semi-synthetic glycosaminoglycan ethers (“SAGEsâ€?). The synthesis of sulfated alkylated and fluoroalkylated SAGEs is also described.

    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:US-6593347-B2
    优先权日:1998-10-30
    标题 :Nitrosated and nitrosylated nonsteroidal antiinflammatory compounds, compositions and methods of use
    发明人:BANDARAGE UPUL K; DONG QING; FANG XINQIN; GARVEY DAVID S; MERCER GREGORY J; RICHARDSON STEWART K; SCHROEDER JOSEPH D; WANG TIANSHENG
    权利人:NITROMED INC
    摘要:The present invention describes novel nitrosated and/or nitrosylated nonsteroidal antiinflammatory compounds, and novel compositions comprising at least one nitrosated and/or nitrosylated nonsteroidal antiinflammatory compound, and, optionally, at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase. The present invention also provides methods for treating, preventing and/or reducing inflammation, pain, and fever; decreasing or reversing the gastrointestinal, renal and other toxicities resulting from the use of nonsteroidal antiinflammatory drugs; treating and/or preventing gastrointestinal disorders; treating inflammatory disease states and disorders; and treating and/or preventing ophthalmic diseases or disorders.
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    主要参考文献


    1: Peraman R, Bhadraya K, Reddy YP, Reddy CS, Lokesh T. Analytical Quality by Design Approach in RP-HPLC Method Development for the Assay of Etofenamate in Dosage Forms. Indian J Pharm Sci. 2015 Nov-Dec;77(6):751-7.
    2: Espasandín-Arias M, Vázquez-Osorio I, Salgado-Boquete L, Rodríguez-Granados MT, Toribio J. Prolonged localized photosensitivity following allergic and photo-aggravated contact dermatitis from etofenamate. Photodermatol Photoimmunol Photomed. 2014 Dec;30(6):340-2. doi: 10.1111/phpp.12130. Epub 2014 Aug 13. doi: 10.3109/10837450.2014.915571. Epub 2014 May 5. doi: 10.3797/scipharm.1305-19. eCollection 2013 Dec.
    6: Orbak Z, Yildirim ZK, Sepetci O, Karakelleoglu C, Alp H. Adverse reaction of topical etofenamate: petechial eruption. West Indian Med J. 2012 Oct;61(7):767-9. doi: 10.5543/tkda.2012.03592. Turkish. doi: 10.1111/j.1600-0536.2011.01920.x. doi: 10.3109/15563651003796374. doi: 10.1111/j.1600-0536.2009.01565.x. doi: 10.1111/j.1600-0536.2007.01190.x. Spanish. Spanish. Review.

    合成参考文献


    参考文献:10.1111/j.1600-0536.2011.01920.x
    摘要:Kerr A, Becher G, Ibbotson S, Ferguson J. Action spectrum for etofenamate photoallergic contact dermatitis. Contact Dermatitis. 2011 Aug;65(2):117–8. doi: 10.1111/j.1600-0536.2011.01920.x.
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