CAS: 479-92-5; 4-Isopropyl-1,5-Dimethyl-2-Phenyl-1H-Pyrazol-3(2H)-One

该化合物是非类固醇抗炎药物,主要用于其止痛和抗热特性,属于丙酮类化合物,经常用于治疗疼痛和发烧;丙苯酚区的化学结构具有助长其药理活动的丙洛酮环的化学结构;通常以口服形式进行,以其相对迅速的行动开始为人所知;丙苯酚区的特点是其中度溶液在水中,高溶液在有机溶剂中,影响其配方的药剂;虽然它有效减轻疼痛,但必须监测潜在的副作用,包括胃肠扰动和过敏反应;由于安全考虑,其使用在某些地区有所减少,并可能受到监管检查.

结构式图片

欧盟法规

ECHA物质ECHA物质化妆品禁用物质清单C&L通报REACH预注册

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CAS号50993-68-5 N-desmethylprop... | CAS号77-78-1 硫酸二甲酯 | CAS号881-05-0 5-methyl-2-phen... | CAS号38604-70-5 N-methyl-N-phen... | CAS号22123-18-8 4-isopropyl-5-m... | CAS号298-12-4 乙醛酸 | CAS号1672-63-5 4-羟基-1,5-二甲基-2-... | CAS号50871-97-1 5-hydroxy-1,5-d... | CAS号89080-91-1 2-acetyl-3-meth... | CAS号105798-28-5 2-Hydroxy-2-iso...

合成工艺路线路线简述

    N-去甲基异丙安替比林 反应生成 异丙安替比林
    参考文献:Paryjczak,T.;Grzywna,R.;Falak,B.;Kozakiewicz,A.;Kotlicki,S.;Pieta,S+
    标题:Paryjczak,T.;Grzywna,R.;Falak,B.;Kozakiewicz,A.;Kotlicki,S.;Pieta,S+

    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-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:US-7186709-B2
    优先权日:2002-08-27
    标 题:Dihydropyrancarboxamides and uses thereof
    发明人:SCHREIBER STUART L; STAVENGER ROBERT A; MITCHISON TIMOTHY J; MALIGA ZOLTAN
    权利人:HARVARD COLLEGE
    摘要:The present invention provides novel dihydropyrancarboxamide compounds of formula (I): n nand collections of these compounds, and provides methods for the synthesis of these compounds; wherein R 1 –R 6 are as defined herein. Additionally, the present invention provides pharmaceutical compositions and methods for treating disorders such as proliferative diseases, and cancer, to name a few.

    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
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    主要参考文献


    1: Radwan MF, Dalby KN, Kaoud TS. Propyphenazone-based analogues as prodrugs and selective cyclooxygenase-2 inhibitors. ACS Med Chem Lett. 2014 Jun 23;5(9):983-8. doi: 10.1021/ml500156v.
    2: Yegles M, Wenning R. Incorporation of propyphenazone in beard hair of a migraine patient. Forensic Sci Int. 2000 Jan 10;107(1-3):233-7. doi: 10.1016/s0379-0738(99)00174-7. 10 Suppl 2(Suppl 2):299S-308S. doi: 10.1111/j.1365-2125.1980.tb01813.x.
    4: Brogden RN. Pyrazolone derivatives. Drugs. 1986;32 Suppl

    合成参考文献


    摘要:Schweizerische Medizinische Wochenschrift., 84(351), 1954 []
    摘要:S72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI:10.5281/zenodo.3955664
    摘要:M. Pesak, O. Greksakova, P. Kopecky and J. Celechovsky. Coll. Czech. Chem. Comm. 32, 2031 (1967).
    参考文献:10.1007/bf00203781|10.1007/s002280050035
    摘要:Kraetsch HG, Hummel T, Ltsch J, Kussat R, Kobal G. Analgesic effects of propyphenazone in comparison to its combination with caffeine. European Journal of Clinical Pharmacology. 1996 Feb 01;49(5):377–82. doi: 10.1007/s002280050035.
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