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CO5150219A1 - Inhibidores de metaloproteasa que contiene alquenilo y alque nilo que son efectivos en el tratamiento de condiciones ca- racterizadas por actividad excesiva de estas enzimas - Google Patents

Inhibidores de metaloproteasa que contiene alquenilo y alque nilo que son efectivos en el tratamiento de condiciones ca- racterizadas por actividad excesiva de estas enzimas

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Publication number
CO5150219A1
CO5150219A1 CO00015564A CO00015564A CO5150219A1 CO 5150219 A1 CO5150219 A1 CO 5150219A1 CO 00015564 A CO00015564 A CO 00015564A CO 00015564 A CO00015564 A CO 00015564A CO 5150219 A1 CO5150219 A1 CO 5150219A1
Authority
CO
Colombia
Prior art keywords
heterocycloalkyl
cycloalkyl
hydrogen
independently selected
alque
Prior art date
Application number
CO00015564A
Other languages
English (en)
Inventor
Michael George Natchus
Roger Charles Bookland
Gregory Almstead Neil
Pikul Stanislaw
De Biswanath
Cheng Menyan
Original Assignee
Procter & Gamble
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Procter & Gamble filed Critical Procter & Gamble
Publication of CO5150219A1 publication Critical patent/CO5150219A1/es

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/32Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D207/33Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D207/337Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
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Abstract

La presente invención se refiere a un compuesto que tiene una estructura según la Fórmula (I)<EMI FILE="00015564_1" ID="1" IMF=JPEG >en donde:(A) X se selecciona de -OH y -NHOH;(B) W se selecciona de -S-, -O-, -N(R33), -C(R33)=C(R33´)-, -N=C(R33)-, y -N=N-,(C) R1 es -(CR6R6´)/R34,(O) R2 es -(CR7R7´)m-R35,(E) R3 es -(CR8R8´)n-R9,(F) R4 es -(CR10R10´)z-A ´-(CR10" R10"´)o-R11.(G) Cada R5 y R5´ se selecciona independientemente de hidrógeno, alquilo, alquenilo, alquinilo, arilo, heteroalquilo, heteroarilo, cicloalquilo, heterocicloalquilo, halógeno, haloalquilo, hidroxi, y alcoxi; y k es de O a aproximadamente 4;(H) A se selecciona de<EMI FILE="00015564_2" ID="2" IMF=JPEG >donde cada R12 y R12´ se selecciona independiente de hidrógeno, alquilo, alquenilo, alquinilo, haloalquilo, arilo, heteroalquilo, heteroarilo, heterocicloalquilo, cicloalquilo, halógeno y -CONR13R13´,(I) G se selecciona de:(1) hidrógeno;(2) -(CR14R14´)p-R15,(3) -(CR16R16´)q-Y-(CR17R17´)r-R18,(4) -CONR37R37´(5) -(CR19R19´)s-NR20R20´,(J) Z se selecciona de:(1) cicloalquilo y heterocicloalquilo;- 2 -(2) -D-(CR26R26´)uR27,(3) -NR29R29´,<EMI FILE="00015564_3" ID="3" IMF=JPEG >(4) , donde(a) E y J se seleccionan independientemente de -CH- y -N-;(b) L se selecciona de -S-, -O-, -N(R38)-, -C(R38)=C(R38´)-, N=C(R38)-, y -N=N-,(c) w es de 0 a aproximadamente 4;(d) cada R36 y R36´ se selecciona en forma independiente de hidrógeno, alquilo, alquenilo, alquinilo, arilo, heteroalquilo, heteroarilo, cicloalquilo, heterocicloalquilo, halógeno, haloalquilo, hidroxi, y alcoxi;(e) M se selecciona de un enlace covalente, -0-, -SOx, -C(O)-, -C(0)NR39-, -NR39-, y -NR39C(0)-;(f) T es -(CR40R40´)y-R41,o un isómero óptico, diasterómero o enantiómero para la Fórmula (I), o una sal farmacéuticamente aceptable, o amida, éster o imida biohidrolizable de los mismos.
CO00015564A 1999-03-03 2000-03-03 Inhibidores de metaloproteasa que contiene alquenilo y alque nilo que son efectivos en el tratamiento de condiciones ca- racterizadas por actividad excesiva de estas enzimas CO5150219A1 (es)

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