CAS: 159700-58-0; (1R,2S)-1-Amino-2-Vinylcyclopropane-1-Carboxylic Acid

该化合物是一个有机化合物,其特点是环丙烷环结构,这是一个由三名成员组成的碳环结构,以其独特的菌株和活性而闻名.该化合物的特点是一个碳丙烯酸功能组(-COOH)和一个附于一个乙烯组(乙烯组)的氨基酸组(-NH2),有助于其作为有机合成的建筑块的潜力.该名称表示具体的立体化学学,它可以影响该化合物的再活动以及与生物系统的互动.由于该化合物具有模拟天然产品的能力,因此经常研究该化合物在制药和农用化学化学中的应用.氨基和箱酸功能的存在表明,该化合物可能表现出诸如极溶剂溶解性以及氢联产潜力等特性,从而影响该化合物在各种化学反应和生物相互作用中的行为.

结构式图片

相似化合物

3095621-03-4 159622-10-3 259214-55-6

上下游产品

(1R,2S)-1-amino-2-vinyl-cyclopropyl carboxylic acid methyl ester (1R,2S)-1-amino-2-vinylcyclopropane carboxylic acid methyl ester tosylate salt (1R,2S)-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylic acid rac-(1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid ethyl ester(1R,2S)-1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acid methyl ester (1R,2S)-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylic acid

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    专利信息


    专利号:US-8591878-B2
    优先权日:2008-02-25
    标 题:Therapeutic compounds
    发明人:MCCAULEY JOHN A; LIVERTON NIGEL J; HARPER STEVEN; MCINTYRE CHARLES J; RUDD MICHAEL T
    权利人:MCCAULEY JOHN A; LIVERTON NIGEL J; HARPER STEVEN; MCINTYRE CHARLES J; RUDD MICHAEL T; MERCK SHARP & DOHME; ANGELETTI P IST RICHERCHE BIO
    摘要:A class of macrocyclic compounds of formula (I), wherein R 1 , R 3 , R 4 , R a , R b , A, B, Z, M, W and n are defined herein, that are useful as inhibitors of viral proteases, particularly the hepatitis C virus (HCV) NS3 protease, are provided. Also provided are processes for the synthesis and use of such macrocyclic compounds for treating or preventing HCV infection.

    专利号:US-8278322-B2
    优先权日:2005-08-01
    标题 :HCV NS3 protease inhibitors
    发明人:HOLLOWAY M KATHARINE; LIVERTON NIGEL J; MCCAULEY JOHN A; RUDD MICHAEL T; VACCA JOSEPH P; LUDMERER STEVEN W; OLSEN DAVID B
    权利人:HOLLOWAY M KATHARINE; LIVERTON NIGEL J; MCCAULEY JOHN A; RUDD MICHAEL T; VACCA JOSEPH P; LUDMERER STEVEN W; OLSEN DAVID B; MERCK SHARP & DOHME
    摘要:The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.

    专利号:US-8309540-B2
    优先权日:2006-10-24
    标 题:HCV NS3 protease inhibitors
    发明人:LIVERTON NIGEL J; VACCA JOSEPH P; MCCAULEY JOHN A; ROMANO JOSEPH J; RUDD MICHAEL T
    权利人:LIVERTON NIGEL J; VACCA JOSEPH P; MCCAULEY JOHN A; ROMANO JOSEPH J; RUDD MICHAEL T; MERCK SHARP & DOHME
    摘要:The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections. (I)

    专利号:US-8927569-B2
    优先权日:2007-07-19
    标 题 :Macrocyclic compounds as antiviral agents
    发明人:HARPER STEVEN; SUMMA VINCENZO; LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; DI FILIPPO MARCELLO; DI FRANCESCO MARIA EMILIA; FERRARA MARCO; ROMANO JOSEPH J; RUDD MICHAEL T
    权利人:HARPER STEVEN; SUMMA VINCENZO; LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; DI FILIPPO MARCELLO; DI FRANCESCO MARIA EMILIA; FERRARA MARCO; ROMANO JOSEPH J; RUDD MICHAEL T; MERCK SHARP & DOHME
    摘要:A class of macrocyclic compounds of formula (I), wherein R 1 , R 3 , R 4 , R a , R b , A, Z, Y, X, M, W, n and m are defined herein, that are useful as inhibitors of viral proteases, particularly the hepatitis C virus (HCV) NS3 protease, are provided. Also provided are processes 5 for the synthesis and use of such macrocyclic compounds for treating or preventing HCV infection. Formula (I):

    专利号:US-8461107-B2
    优先权日:2008-04-28
    标题:HCV NS3 protease inhibitors
    发明人:LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; GILBERT KEVIN F; MCINTYRE CHARLES J; RUDD MICHAEL T
    权利人:LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; GILBERT KEVIN F; MCINTYRE CHARLES J; RUDD MICHAEL T; MERCK SHARP & DOHME
    摘要:The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.

    专利号:US-8377874-B2
    优先权日:2006-10-27
    标题 :HCV NS3 protease inhibitors
    发明人:LIVERTON NIGEL J; VACCA JOSEPH P; MCCAULEY JOHN A; RUDD MICHAEL T
    权利人:MERCK SHARP & DOHME; LIVERTON NIGEL J; VACCA JOSEPH P; MCCAULEY JOHN A; RUDD MICHAEL T
    摘要:The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.
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    合成参考文献


    参考文献:10.1055/s-2006-955757
    摘要:Yee N, Farina V, Donsbach K. Synthesis of BILN 2061. Synfacts. 2007 Feb;2007(2):0125. doi: 10.1055/s-2006-955757.
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