COMPUESTOS DERIVADOS DE PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA COMO INHIBIDORES DE LA ENZIMA INTEGRASA DE VIH
SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C8), ALQUENILO(C2-C8) O HETEROALQUILO(C1-C8) OPCIONALMENTE SUSTITUIDOS CON HALO, CN, ALQUILO(C1-C8), ENTRE OTROS; R2 ES H O ALQUILO(C1-C8); R3 ES ALQUILO(C1-C8), HETEROALQUILO(C1-C8), ARILO(C6-C14), ENTRE OTROS; Z ES -(CR4R4)n- DONDE R...
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Main Authors | , , , , |
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Format | Patent |
Language | Spanish |
Published |
13.06.2007
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Subjects | |
Online Access | Get full text |
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Abstract | SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C8), ALQUENILO(C2-C8) O HETEROALQUILO(C1-C8) OPCIONALMENTE SUSTITUIDOS CON HALO, CN, ALQUILO(C1-C8), ENTRE OTROS; R2 ES H O ALQUILO(C1-C8); R3 ES ALQUILO(C1-C8), HETEROALQUILO(C1-C8), ARILO(C6-C14), ENTRE OTROS; Z ES -(CR4R4)n- DONDE R4 ES H, HALO, ALQUILO(C1-C8), CICLOALQUILO(C3-C8), ENTRE OTROS; R5 ES H, HETEROALQUILO(C1-C8), ARILO(C6-14), ALQUENILO(C2-C8), ENTRE OTROS; R6 ES H. SON COMPUESTOS PREFERIDOS: 8-BUTIL-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7,8,9-TETRAHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 3-(4-FLUOROBENCIL)-7-HIDROXI-1-({[(2S)-2-HIDROXIPROPIL]AMINO}METIL)-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 1-{[ETIL(METIL)AMINO]METIL}-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ENZIMA INTEGRASA DEL VIRUS DE INMUNODEFICIENCIA HUMANA (VIH) SIENDO UTILES EN EL TRATAMIENTO DE SIDA
The present invention is directed to compounds of formula (I), and pharmaceutically acceptable salts and solvates thereof, their synthesis, and their use as modulators or inhibitors of the human immunodeficiency virus ("HIV") integrase enzyme. |
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AbstractList | SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C8), ALQUENILO(C2-C8) O HETEROALQUILO(C1-C8) OPCIONALMENTE SUSTITUIDOS CON HALO, CN, ALQUILO(C1-C8), ENTRE OTROS; R2 ES H O ALQUILO(C1-C8); R3 ES ALQUILO(C1-C8), HETEROALQUILO(C1-C8), ARILO(C6-C14), ENTRE OTROS; Z ES -(CR4R4)n- DONDE R4 ES H, HALO, ALQUILO(C1-C8), CICLOALQUILO(C3-C8), ENTRE OTROS; R5 ES H, HETEROALQUILO(C1-C8), ARILO(C6-14), ALQUENILO(C2-C8), ENTRE OTROS; R6 ES H. SON COMPUESTOS PREFERIDOS: 8-BUTIL-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7,8,9-TETRAHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 3-(4-FLUOROBENCIL)-7-HIDROXI-1-({[(2S)-2-HIDROXIPROPIL]AMINO}METIL)-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 1-{[ETIL(METIL)AMINO]METIL}-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ENZIMA INTEGRASA DEL VIRUS DE INMUNODEFICIENCIA HUMANA (VIH) SIENDO UTILES EN EL TRATAMIENTO DE SIDA
The present invention is directed to compounds of formula (I), and pharmaceutically acceptable salts and solvates thereof, their synthesis, and their use as modulators or inhibitors of the human immunodeficiency virus ("HIV") integrase enzyme. |
Author | ZHU HUICUN JOHNSON TED WILLIAM DRESS KLAUS RUPRECHT PLEWE MICHAEL BRUNO TANIS STEVEN PAUL |
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Snippet | SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C8), ALQUENILO(C2-C8) O HETEROALQUILO(C1-C8) OPCIONALMENTE SUSTITUIDOS CON HALO, CN,... |
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Title | COMPUESTOS DERIVADOS DE PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA COMO INHIBIDORES DE LA ENZIMA INTEGRASA DE VIH |
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