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【发明公布】硼酰基取代的苯丙氨酸药用前体及其合成方法和BNCT疗法的配套用途_吴卫东_202210715060.6 

申请/专利权人:吴卫东

申请日:2022-05-20

公开(公告)日:2023-10-13

公开(公告)号:CN116874508A

主分类号:C07F5/02

分类号:C07F5/02;A61K9/06;A61K9/08;A61K9/20;A61K9/48;A61K31/69;A61P31/00;A61P31/12;A61P35/00

优先权:

专利状态码:在审-实质审查的生效

法律状态:2023.10.31#实质审查的生效;2023.10.13#公开

摘要:本发明专利涉及药物化学和辐射医学研究领域,主要涉及硼酰基取代的苯丙氨酸药用前体的化学结构式、合成方法及其BNCT疗法配套用途的研究范畴;本作者提交了3‑[4^‑[二‑[四氢吡咯基]‑[硼酰基]]‑1^‑[苯基]]‑2‑[二‑[四氢吡咯基]‑[硼酰基]‑[胺基]]‑L‑[丙酰基]‑[四氢吡咯基],并且命名它为奥特铂瑞;本作者提交了硼酰基取代的苯丙氨酸药用前体的结构通式、化学结构式、合成方法、组合物剂型、抗癌抗病毒领域的用途及其与BNCT中子源设备的配套医学用途。

主权项:1.一种硼酰基取代的苯丙氨酸前体共同符合的结构通式: 结构通式中的细线代表化学键,英文字母代表从下列基团定义中任一挑选出的化合物基团: 基团定义 01E选自:-C,-CH,-CH2,-C2H4;02D选自:-H,-O,-CH3,-C2H5,-C3H7;03S选自:-H,-CH,-B,-C2H4,-CH2,-C,-OH;04A选自:-H,-O,-CFH2,-CF2H,-S,-B,-CN,-NH2;05W选自:-H,-NH,-CFH2,-C4H8N,-B,-CF3,-C4H4N,-NH2;06U选自:-H,-NH,-CFH2,-C4H8N,-OH,-CF3,-C4H4N,-CN,-NH2;07V选自:-H,-NH,-CFH2,-C4H8N,-CF3,-OH,-C4H4N,-CN,-NH2;08M选自:-H,-F,-CFH2,-CF2H,-CF3,-CN,-CH3,-C2H5,-C3H7;09Q选自:-H,-F,-O,-CF2H,-NH,-CF3,-CO,-CH3,-C2H5,-C3H7;10K选自:-H,-CH2,-C2H4,-CO,-OH,-N3,-N,-NH2,-H,-NH;11Y选自:-H,-C4H8N,-CF3,-C4H4N,-OH,-CN,-NH2;12X选自:-H,-CO,-N,-F,-CFH2,-NH,-CF2H,-CF3,-C,-CN,-NH2;13R选自:-H,-OH,-CH3,-C2H5,-C3H7,-C4H9,-C5H11,-C6H13,-C7H15;-C8H17,-C9H19,-C6H5,-C7H7,-OCH3,-OC2H5,-OCH3H7,-OC4H9;-O-C5H11,-O-C6H13,-O-C7H15,-O-C8H17,-C4H8N,-CF3,-C4H4N;-O-C3H5,-O-C4H7,-O-C5H9,-O-C6H11,-O-C7H13,-O-C8H17;-NH-CH2-CO-O-CH3,-NH-CH2-COO-C2H5,-NH-CH2COO-C3H7;-NH-CH2-COO-C4H9,-NH-CH2-COOC5H11,-NH-CH2-COO-C6H13;-NH-CH2-COO-C7H15,-NH-C2H4COO-CH3,-NHC2H4-COO-C2H5;-NH-C2H4-COOC3H7,-NH-C2H4-COOC4H9,-NH-C2H4COO-C5H11;-NH-C2H4-COOC6H13,-NH-C2H4-COOC7H15,-NH-C3H6COO-CH3;-NH-C3H6COOC2H5,-NH-C3H6-COO-C3H7,-NH-C3H6COO-C4H9;-NH-C3H6COOC5H11,-NH-C3H6COOC6H13,-NH-C3H6-COOC7H15;-NH-C4H8COO-CH3,-NH-C4H8-COOC2H5,-NH-C4H8-COO-C3H7;-NH-C4H8COOC4H9,-NH-C4H8COO-C5H11,-NH-C4H8COO-C6H13;-NH-C4H8COO-C7H15,-NH-C5H10COO-CH3,-NH-C5H10COOC2H5;-NH-C5H10COOC3H7,-NH-C5H10COOC4H9,-NH-C5H10-COOC5H11;14T选自:-H,-OH,-CH3,-C2H5,-C3H7,-C4H9,-C5H11,-C6H13,-C7H15;-C8H17,-C9H19,-C6H5,-C7H7,-OCH3,-OC2H5,-OCH3H7,-OC4H9;-O-C5H11,-O-C6H13,-O-C7H15,-O-C8H17,-C4H8N,-CF3,-C4H4N;-O-C3H5,-O-C4H7,-O-C5H9,-O-C6H11,-O-C7H13,-O-C8H17;-NH-CH2-CO-O-CH3,-NH-CH2-COO-C2H5,-NH-CH2COO-C3H7;-NH-CH2-COO-C4H9,-NH-CH2-COOC5H11,-NH-CH2-COO-C6H13;-NH-CH2-COO-C7H15,-NH-C2H4COO-CH3,-NHC2H4-COO-C2H5;-NH-C2H4-COOC3H7,-NH-C2H4-COOC4H9,-NH-C2H4COO-C5H11;-NH-C2H4-COOC6H13,-NH-C2H4-COOC7H15,-NH-C3H6COO-CH3;-NH-C3H6COO-C2H5,-NH-C3H6-COO-C3H7,-NH-C3H6COO-C4H9;-NH-C3H6COO-C5H11,-NH-C3H6COOC6H13,-NH-C3H6-COOC7H15;-NH-C4H8COO-CH3,-NH-C4H8-COOC2H5,-NH-C4H8-COO-C3H7;-NH-C4H8COOC4H9,-NH-C7H14COOC5H11,-NH-C7H14COOC6H13;-NH-C4H8COO-C7H15,-NH-C5H10COO-CH3,-NH-C5H10COOC2H5。

全文数据:

权利要求:

百度查询: 吴卫东 硼酰基取代的苯丙氨酸药用前体及其合成方法和BNCT疗法的配套用途

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