CAS: 57292-45-2; Boc-D-Phe(4-F)-Oh

该化合物是(2R)配置的手性中心.乙型丁氧碳基(Boc)组的存在表明,它很可能被用作浸泡合成的保护群体,提高了其在有机化学中的效用.四氟苯基分子引入氟基原子,可以影响化合物的电子特性和生物活动.作为丙酸衍生物,它拥有酸性和基本功能组,允许各种化学环境中的潜在互动.该化合物的溶性,稳定性和再活性可因pH和溶剂条件而异,使其在制药和生物化学应用中具有多种特性.

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2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile L-4-fluorophenylalanine tert-butyl dicarbonatedi-tert-butyl dicarbonate 4-Fluorophenylalaninetert-butyl N-[(1S)-1-[(4-fluorophenyl)methyl]-2-[methoxy(methyl)amino]-2-oxo-ethyl]carbamate (S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-fluoro-phenyl)-propionylamino]-acetylamino}-acetylamino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid; hydr°Chloride (S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-acetylamino}-acetylamino)-3-(4-fluoro-phenyl)-propionylamino]-4-methyl-pentanoic acid; hydr°Chloride B°C-Phe(4-F)-NMeBzl

合成工艺路线路线简述

    📜Methyl (R)-2-Tert-Butoxycarbonylamino-3-(4-Fluorophenyl)Propanoate置于水,Lithium Hydroxide体系中,用 四氢呋喃,甲醇 作为反应溶剂,化学反应 6.0H,反应生成 Boc-D-4-氟苯丙氨酸
    参考文献:Discovery Of Pyrrolopyrimidine Inhibitors Of Akt
    标题:Discovery Of Pyrrolopyrimidine Inhibitors Of Akt
    摘要:The Discovery And Optimization Of A Series Of Pyrrolopyrimidine Based Protein Kinase B (Pkb/akt) Inhibitors Discovered Via Hts And Structure Based Drug Design Is Reported. The Compounds Demonstrate Potent Inhibition Of All Three Akt Isoforms And Knockdown Of Phospho-Pras40 Levels In Lncap Cells And Tumor Xenografts. (C) 2010 Elsevier Ltd. All Rights Reserved.
    DOI:10.1016/j.Bmcl.2010.08.053

    海关参考信息

    专利信息


    专利号:US-6514997-B2
    优先权日:1999-12-03
    标题:Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis
    发明人:DRAGOVICH PETER S; PRINS THOMAS J; ZHOU RU; JOHNNSON JR THEODORE O
    权利人:AGOURON PHARMA
    摘要:Compounds of the formula: n where the formula variables are as defined herein, are disclosed that advantageously inhibit or block the biological activity of the picornaviral 3C protease. Also disclosed are compounds of the formula: n where the formula variables are as defined herein that advantageously inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with one or more picornaviruses, such as rhinovirus 3C proteases. Intermediates and synthetic methods for preparing such compounds are also described.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    合成方法参考DOI号:10.1021/acs.jmedchem.9b00002
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