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依鲁替尼合成路线图解 被引量:2

Graphical synthetic routes of ibrutinib
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摘要 抗肿瘤药依鲁替尼(ibrutinib,1)化学名称为1-[(3R)-3-[4-氨基-3-(4-苯氧基苯基)-1H-吡唑并[3,4-d]嘧啶-1-基]-1-哌啶基]-2-丙烯-1-酮,分子式:C_(25)H_(24)N_6O_2,CAS登记号:936563-96-1。依鲁替尼是由Johnson Johnson公司和Pharmacyclics公司合作研发的靶向抗癌新药,于2013年12月在美国上市,2014年10月在欧洲上市,但尚未在国内上市,其专利保护期至2026年12月。 Ibrutinib is an inhibitor of bruton's tyrosine kinase,which is approved for the treatment of relapsed/refractory mantle cell lymphoma(MCL),orchronic lymphocytic leukaemia(CLL)and CLL patients with del 17 p or TP53 mutation.This article summarizes the synthetic methods of ibrutinib from different materials.
出处 《中国药物化学杂志》 CAS CSCD 2016年第1期71-73,7,共3页 Chinese Journal of Medicinal Chemistry
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参考文献13

  • 1田野,郭春.依鲁替尼[J].中国药物化学杂志,2014,24(3):254-254. 被引量:2
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二级参考文献4

  • 1US FDA.lbrutinib [EB/OL].[2013-11-13].http://www.fda.gov/drugs/informationondrugs/approveddrugs/ucm374857.htm.
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  • 4Pharmacyclics,Inc.Full prescribing information [EB/OL].[2013-11-13].http://www.accessdata.fda.gov/drugsatf-da_docs/label/2013/2055521b1.pdf.

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