CAS: 599-33-7; Prednisolon

该化合物是合成的花生类固醇, 具有抗炎和免疫抑制特性,主要用于治疗各种炎症和自体免疫紊乱,其特点是能够调节免疫反应,并通过抑制亲炎性细胞内皮和其他调解人来减少炎症; Prednylidene通常在时尚配方中施用,允许在最低限度的系统吸收下进行局部治疗; 其化学结构包括类固醇脊柱,在皮质类固醇中很常见,有助于其生物活动; 乳腺前叶的药代动因学主要涉及肝脏的代谢,通过尿液排泄出. 与其他园艺类固醇类机器人一样,潜在的副作用可能包括皮肤刺激,荷尔蒙性失调和对感染的敏感度增加,从而需要在治疗期间进行仔细监测.

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      专利号:US-12391691-B2
      优先权日:2018-11-16
      标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
      发明人:PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
      权利人:AMGEN INC
      摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

      专利号:US-2025206736-A1
      优先权日:2019-11-14
      标题 :Synthesis of kras g12c inhibitor compound
      发明人:CORBETT MICHAEL THOMAS; CAILLE SEBASTIEN
      权利人:AMGEN INC
      摘要:The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

      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-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:WO-0112817-A1
      优先权日:1999-08-12
      标题:Evolution and use of enzymes for combinathorial and medicinal chemistry
      发明人:KREBBER CLAUS; DAVIS S CHRISTOPHER; DELCARDAYRE STEPHEN; SELIFONOV SERGEY A; HOWARD RUSSELL
      权利人:MAXYGEN INC; LIU LU; KREBBER CLAUS; DAVIS S CHRISTOPHER; DELCARDAYRE STEPHEN; SELIFONOV SERGEY A; HOWARD RUSSELL
      摘要:This invention provides libraries of recombinant derivatizing enzymes that are useful for biocatalytic synthesis of derivatives oforganic molecules, including lead compounds for pharmaceutical use. The recombinant derivatizing enzymes catalyze reactions such as modification or replacement of functional groups on the organicmolecules, or addition of chemical moieties onto preexisting functional groups. The use of recombinant enzyme libraries enables one to obtain enzymes that catalyze the formation of organic molecule derivatives that could not otherwise be made using only naturally occurring enzymes.

      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

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      主要参考文献


      1: Shar PA, Tao W, Gao S, Huang C, Li B, Zhang W, Shahen M, Zheng C, Bai Y, Wang Y. Pred-binding: large-scale protein-ligand binding affinity prediction. J Enzyme Inhib Med Chem. 2016 Dec;31(6):1443-50. doi: 10.3109/14756366.2016.1144594. Epub 2016 Feb 18. doi: 10.1007/s00595-014-1073-3. Epub 2014 Nov 6. doi: 10.1016/j.pediatrneurol.2013.07.022. Epub 2013 Oct 15. Japanese. Epub 2005 Oct 1. German. German. German. French.

      合成参考文献


      摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
      参考文献:10.2165/00044011-199816060-00004
      摘要:Claesson CB, Schmidt IK. Drug use in Swedish nursing homes. Clin Drug Investig. 1998;16(6):441–52. doi: 10.2165/00044011-199816060-00004.
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