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Hepatitis C virus inhibitors
专利权人:
BRISTOL-MYERS SQUIBB COMPANY
发明人:
LOPEZ OMAR D.,CHEN QI,BELEMA MAKONEN,HAMANN LAWRENCE G.
申请号:
PE2011001733
公开号:
PE20120517A1
申请日:
2010.03.29
申请国别(地区):
PE
年份:
2012
代理人:
摘要:
It's an abiotic formula compound,S is 0 or 1, l is - L1-L2L1 and L2 are cyclohexane, phenyl, cyclohexane, etc.; ey'son o'nh; R1 is h or C (o) RX; R2 is h or C (o) ry; RX and ry are cyclohexane c3-c8; C1-C10 Cypress oil layer; c1-c1-c10 acoxy C10, etc.; R100 and R110 are h, C1-C10 Cypress oil layer, C1-C10 cyano-c10 and halogen. The most popular compounds are ((1s) - 1 - ((2S) - 2 - (4 - (2 - ((2S) - 1 -) ((2S) - 2 - ((methoxy) amine) - 3-methylbutanol-2-pyridine-1 '- Bi (3-cyclohexane-1-il) - 4-il) - 1-bi (3-cyclohexane-1-il) - 1-pyridine-methanol-2-il) - 1((1s) - 2 - ((2S) - 2 - (4 - (2 - ((2S) - 1 - (n -) (methoxy) 1 - (n - (methoxy) 1 - (n -) - 1 - (pyridan) - 1-pyridan-4-1) - 1,1 '- Bi (3-cyclohexane-1-1) A pharmaceutical composer was also mentioned These compounds inhibit the NS5A protein encoded by hepatitis C virusREFERIDA A UN COMPUESTO HETEROCICLICO DE FORMULA (I), DONDE s ES 0 O 1; L ES -L1-L2-; L1 Y L2 SON CICLOHEXILO, FENILO, CICLOHEXENO, ENTRE OTROS; Y E Y' SON O O NH; R1 ES H O C(O)Rx; R2 ES H O C(O)Ry; Rx Y Ry SON CICLOALQUILO C3-C8; ALQUILO C1-C10; ALCOXI C1-C10, ENTRE OTROS; R100 Y R110 SON H, ALQUILO C1-C10, CIANOALQUILO C1-C10 Y HALO. SON COMPUESTOS PREFERIDOS: ((1S)-1-(((2S)-2-(4-(4'-(2-((2S)-1-((2S)-2-((METOXICARBONIL)AMINO)-3-METILBUTANOIL-2-PIRROLIDINIL)-1H-IMIDAZOL-4-IL)-1,1'-BI(3-CICLOHEXEN-1-IL)-4-IL)-1H-IMIDAZOL-2-IL)-1-PIRROLIDINIL)CARBONIL)-2-METILPROPIL)CARBAMATO DE METILO, ((1S)-2-((2S)-2-(4-(4'-(2-((2S)-1-(N-(METOXICARBONIL)-L-ALANIL)-2-PIRROLIDINIL)-1H-IMIDAZOL-4-IL)-1,1'-BI(3-CICLOHEXEN-1-IL)-4-IL)-1H-IMIDAZOL-2-IL)-1-PIRROLIDINIL)-1-METIL-2-OXOETIL)CARBAMATO DE METILO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS INHIBEN LA PROTEINA NS5A CODIFICADA POR EL VIRUS DE LA HEPATITIS C
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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