ES2684368T3 - Derivados del nucleósido uridina, composiciones y métodos de uso - Google Patents

Derivados del nucleósido uridina, composiciones y métodos de uso Download PDF

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ES2684368T3
ES2684368T3 ES14775026T ES14775026T ES2684368T3 ES 2684368 T3 ES2684368 T3 ES 2684368T3 ES 14775026 T ES14775026 T ES 14775026T ES 14775026 T ES14775026 T ES 14775026T ES 2684368 T3 ES2684368 T3 ES 2684368T3
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Philip G. Haydon
Jinbo Lee
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    • A61K31/7072Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
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    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
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    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06Pyrimidine radicals
    • C07H19/067Pyrimidine radicals with ribosyl as the saccharide radical

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Abstract

Una composición farmacéutica que comprende un compuesto de fórmula I:**Fórmula** o una sal del mismo, en el que: A es un anillo aromático bicíclico (C5-C10) que tiene hasta 4 heteroátomos seleccionados entre N, O y S, en el que el anillo aromático está independientemente y opcionalmente sustituido con uno o más R7; X se selecciona de: -H, -C(O)R5, -C(O)OR5, y -P(O)(OR5)2; Y es un enlace o un grupo alifático (C1-C5) independientemente y opcionalmente sustituido con uno o más R4; Z y W se seleccionan cada uno independientemente de >=O, >=S, >=N(R5), y >=NOR5; R1 se selecciona de: -H, halógeno, -OR5, -CN, -CF3, -OCF3 y un grupo alifático (C1-C6) opcionalmente sustituido con uno o más R7; R2 y R3 se seleccionan cada uno independientemente de -OR5, -SR5, -NR5R6, -OC(O)R5, -OC(O)NR5R6, y -OC(O)OR5; cada aparición de R4 se selecciona independientemente de: halógeno, -OR5, -NO2, -CN, -CF3, -OCF3, -R5, 1,2-metilendioxi, 1,2-etilendioxi, -N(R5)2, -SR5, -SOR5, -SO2R5, - SO2N(R5)2, -SO3R5, -C(O)R5, -C(O)C(O)R5, -C(O)CH2C(O)R5, -C(S)R5, -C(S)OR5, -C(O)OR5, -C(O)C(O)OR5, - C(O)C(O)N(R5)2, -OC(O)R5, -C(O)N(R5)2, -OC(O)N(R5)2, -C(S)N(R5)2, -(CH2)0-2NHC(O)R5, -N(R5)N(R5)COR5, - N(R5)N(R5)C(O)OR5, -N(R5)N(R5)CON(R5)2, -N(R5)SO2R5, -N(R5)SO2N(R5)2, -N(R5)C(O)OR5, -N(R5)C(O)R5, - N(R5)C(S)R5, -N(R5)C(O)N(R5)2, -N(R5)C(S)N(R5)2, -N(COR5)COR5, -N(OR5)R5, -C(>=NH)N(R5)2, -C(O)N(OR5)R5, - C(>=NOR5)R5, -OP(O)(OR5)2, -P(O)(R5)2, -P(O)(OR5)2, o -P(O)(H)(OR5); cada aparición de R5 se selecciona independientemente de: H-, (C1-C12)-alifático-, (C3-C10)-cicloalquil- o -cicloalquenil-, [(C3-C10)-cicloalquil o -cicloalquenil]-(C1-C12)-alifático-, (C6-C10)-aril-, (C6-C10)-aril-(C1-C12)alifático-, (C3-C10)-heterociclil-, (C6-C10)-heterociclil-(C1-C12)alifático-, (C5-C10)-heteroaril-, y (C5-C10)-heteroaril-(C1-C12)-alifático-; en la que dos grupos R5 unidos al mismo átomo forman opcionalmente un anillo aromático o no aromático de 3 a 10 miembros que tiene hasta 3 heteroátomos seleccionados independientemente de N, O, S, SO o SO2, en la que dicho anillo está opcionalmente fusionado a un arilo (C6-C10), heteroarilo (C5-C10), cicloalquilo (C3-C10), o un heterociclilo (C3-C10); y en la que cada grupo R5 está independientemente y opcionalmente sustituido con uno o más R7; R6 se selecciona de: -R5, -C(O)R5, -C(O)OR5, -C(O)N(R5)2 y -S(O)2R5; cada aparición de R7 se selecciona independientemente de: halógeno, -OR8, -NO2, -CN, -CF3, -OCF3, -R8, oxo, tioxo, 1,2-metilendioxi, 1,2-etilendioxi, -N(R8)2, -SR8, -SOR8, -SO2 R8, -SO2N(R8)2, -SO3R8, -C(O)R8, -C(O)C(O)R8, -C(O)CH2C(O)R8, -C(S)R8, -C(S)OR8, -C(O)OR8, -C(O)C(O)OR8, - C(O)C(O)N(R8)2, -OC(O)R8, -C(O)N(R8)2, -OC(O)N(R8)2, -C(S)N(R8)2, -(CH2)0-2NHC(O)R8, -N(R8)N(R8)COR8, - N(R8)N(R8)C(O)OR8, -N(R8)N(R8)CON(R8)2, -N(R8)SO2R8, -N(R8)SO2N(R8)2, -N(R8)C(O)OR8, -N(R8)C(O)R8, - N(R8)C(S)R8, -N(R8)C(O)N(R8)2, -N(R8)C(S)N(R8)2, -N(COR8)COR8, -N(OR8)R8, -C(>=NH)N(R8)2, -C(O)N(OR8)R8, - C(>=NOR8)R8, -OP(O)(OR8)2, -P(O)(R8)2, -P( O)(OR8)2, o -P(O)(H)(OR8); cada aparición de R8 se selecciona independientemente de: H- y (C1-C6)-alifático- ; y un portador, adyuvante o excipiente farmacéuticamente aceptable.
ES14775026T 2013-03-13 2014-03-13 Derivados del nucleósido uridina, composiciones y métodos de uso Active ES2684368T3 (es)

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