CAS: 2825-60-7; 3-(2-Chloroethoxy)-9-Fluoro-11.β.,16.α.,17,21-Tetrahydroxy-20-Oxopregna-3,5-Diene-6-Carboxaldehyde, Cyclic 16,17-Acetal With Acetone, 21-Acetate

该化合物是一种合成的可口可乐机器人,具有抗炎和免疫抑制特性,主要用于医疗应用,特别是治疗各种炎症和免疫性免疫紊乱,其特点是能够调节免疫反应,从而减少炎症,减轻与过敏,哮喘和某些皮肤紊乱等条件有关的症状; 与凝胶受体结合,形成对凝胶质受体的功能,导致抗炎蛋白的转录,抑制亲炎细胞素; 其致癌性皮质通常包括快速吸收和相对较长的半衰期,允许有效的治疗剂量; 但是,与其他可口可口可乐类机器人一样,它可能会产生副作用,包括对新陈代谢,免疫功能以及长期使用的皮肤完整性的潜在影响; 与任何药物一样,在医学监督下,必须使用可口可接受的代谢,以管理剂量和监测.

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      专利信息


      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-9709067-A1
      优先权日:1995-09-05
      标 题 :Combination of 5-lipoxygenase and leukotriene synthesis inhibitors with glucocorticosteroids
      发明人:BURCHARDT ELMAR-REINHOLD; MUELLER-PEDDINGHAUS REINER
      权利人:BAYER AG; BURCHARDT ELMAR REINHOLD; MUELLER PEDDINGHAUS REINER
      摘要:The combination is disclosed of 5-lipoxygenase inhibitors as direct action lipoxygenase inhibitors (LOI) or of leukotriene synthesis inhibitors (LSI) with glucocorticosteroids (GCS). This combination is suitable for treating and preventing various acute and chronic inflammatory processes, in particular of the respiratory tract, and may therefore be used as a medicament, in particular for treating asthma.

      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: Bertazzoli C, Chieli T, Ricevuti G. Formocortal: studio sperimentale della tollerabilitá acuta e cronica [Formocortal: experimental study of its acute and chronic toxicity]. Eur J Toxicol. 1971 Sep-Oct;4(5):432-40. Italian. 47(4):304-8. doi: 10.1159/000048538. 19(11):620-4. Italian. 45(7):451-62. Italian. 44(12):673-6. Italian.

      合成参考文献


      摘要:Journal Europeen de Toxicologie., 4(88), 1971
      摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
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