CAS: 1073485-20-7; (3-((6-(2-Methoxyphenyl)Pyrimidin-4-yl)Amino)Phenyl)Methanesulfonamide

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(3-aminophenyl)methanesulfonamide 4-chloro-6-(2-methoxy-phenyl)-pyrimidine

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  • 合成目标产物 Ldc000067 主要起始原料 (3-Amino-Phenyl)-Methanesulfonamide And 4-Chloro-6-(2-Methoxy-Phenyl)-Pyrimidine
  • (文献来源)合成步骤主要原料 (3-Amino-Phenyl)-Methanesulfonamide 和 4-Chloro-6-(2-Methoxy-Phenyl)-Pyrimidine
📜3-氨基-苯甲烷磺酰胺,4-Chloro-6-(2-Methoxyphenyl)Pyrimidine 以 N,N-二甲基甲酰胺 用作溶剂,化学反应 1.0H,以71%的收率获得(3-(6-(2-甲氧基苯基)嘧啶-4-基氨基)苯基)甲烷磺酰胺
参考文献:Characterization Of Molecular And Cellular Functions Of The Cyclin-Dependent Kinase Cdk9 Using A Novel Specific Inhibitor
标题:Characterization Of Molecular And Cellular Functions Of The Cyclin-Dependent Kinase Cdk9 Using A Novel Specific Inhibitor
摘要:Background And Purposethe Cyclin‐dependent Kinase Cdk9 Is An Important Therapeutic Target But Currently Available Inhibitors Exhibit Low Specificity And/or Narrow Therapeutic Windows. Here We Have Used A New Highly Specific Cdk9 Inhibitor,Ldc000067 To Interrogate Gene Control Mechanisms Mediated By Cdk9.Experimental Approachthe Selectivity Of Ldc000067 Was Established In Functional Kinase Assays. Functions Of Cdk9 In Gene Expression Were Assessed With In Vitro Transcription Experiments,Single Gene Analyses And Genome‐wide Expression Profiling. Cultures Of Mouse Embryonic Stem Cells,Hela Cells,Several Cancer Cell Lines,Along With Cells From Patients With Acute Myelogenous Leukaemia Were Also Used To Investigate Cellular Responses To Ldc000067.Key Resultsthe Selectivity Of Ldc000067 For Cdk9 Over Other Cdks Exceeded That Of The Known Inhibitors Flavopiridol And Drb. Ldc000067 Inhibited In Vitro Transcription In An Atp‐competitive And Dose‐dependent Manner. Gene Expression Profiling Of Cells Treated With Ldc000067 Demonstrated A Selective Reduction Of Short‐lived Mrnas,Including Important Regulators Of Proliferation And Apoptosis. Analysis Of De Novo Rna Synthesis Suggested A Wide Ranging Positive Role Of Cdk9. At The Molecular And Cellular Level,Ldc000067 Reproduced Effects Characteristic Of Cdk9 Inhibition Such As Enhanced Pausing Of Rna Polymerase Ii On Genes And,Most Importantly,Induction Of Apoptosis In Cancer Cells.Conclusions And Implicationsour Study Provides A Framework For The Mechanistic Understanding Of Cellular Responses To Cdk9 Inhibition. Ldc000067 Represents A Promising Lead For The Development Of Clinically Useful,Highly Specific Cdk9 Inhibitors.
Doi:10.1111/bph.12408

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主要参考文献


1: Xue S, Shao Q, Zhu LB, Jiang YF, Wang C, Xue B, Lu HM, Sang WL, Ma JZ. LDC000067 suppresses RANKL-induced osteoclastogenesis in vitro and prevents LPS-induced osteolysis in vivo. Int Immunopharmacol. 2019 Oct;75:105826. doi: 10.1016/j.intimp.2019.105826. Epub 2019 Aug 19. doi: 10.1016/j.bbrc.2019.07.032. Epub 2019 Jul 13. doi: 10.1096/fj.201801789RR. Epub 2019 Feb 6.
4: Löschmann N, Michaelis M, Rothweiler F, Voges Y, Balónová B, Blight BA, Cinatl J Jr. ABCB1 as predominant resistance mechanism in cells with acquired SNS-032 resistance. Oncotarget. 2016 Sep 6;7(36):58051-58064. doi: 10.18632/oncotarget.11160.
5: Albert TK, Rigault C, Eickhoff J, Baumgart K, Antrecht C, Klebl B, Mittler G, Meisterernst M. Characterization of molecular and cellular functions of the cyclin-dependent kinase CDK9 using a novel specific inhibitor. Br J Pharmacol. 2014 Jan;171(1):55-68. doi: 10.1111/bph.12408.

合成参考文献


参考文献:10.1016/j.ejmech.2015.12.023
摘要:Baltus CB, Jorda R, Marot C, Berka K, Bazgier V, Kryštof V, Prié G, Viaud-Massuard M. Synthesis, biological evaluation and molecular modeling of a novel series of 7-azaindole based tri-heterocyclic compounds as potent CDK2/Cyclin E inhibitors. European Journal of Medicinal Chemistry. 2016 Jan;108():701–19. doi: 10.1016/j.ejmech.2015.12.023.
参考文献:10.1124/mol.119.115964
摘要:Lee TD, Lee OW, Brimacombe KR, Chen L, Guha R, Lusvarghi S, Tebase BG, Klumpp-Thomas C, Robey RW, Ambudkar SV, Shen M, Gottesman MM, Hall MD. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular Pharmacology. 2019 Nov;96(5):629–40. doi: 10.1124/mol.119.115964.
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