BR9809062A - Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses - Google Patents

Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses

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Publication number
BR9809062A
BR9809062A BR9809062-3A BR9809062A BR9809062A BR 9809062 A BR9809062 A BR 9809062A BR 9809062 A BR9809062 A BR 9809062A BR 9809062 A BR9809062 A BR 9809062A
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Brazil
Prior art keywords
group
pharmaceutical
pharmaceutical compositions
compositions containing
cycloalkyl
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BR9809062-3A
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Portuguese (pt)
Inventor
Steven L Bender
Melwyn A Abreo
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Agouron Pharmaceuticlas Inc
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Application filed by Agouron Pharmaceuticlas Inc filed Critical Agouron Pharmaceuticlas Inc
Publication of BR9809062A publication Critical patent/BR9809062A/en

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • C07D213/6432-Phenoxypyridines; Derivatives thereof
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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    • A61P19/00Drugs for skeletal disorders
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    • A61P19/00Drugs for skeletal disorders
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P35/00Antineoplastic agents
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    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C323/52Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
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    • C07C323/51Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/60Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
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    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract

Patente de Invenção: <B>"INIBIDORES DA METALOPROTEINASE, COMPOSIçõES FARMACêUTICAS CONTENDO OS MESMOS E SEUS USOS FARMACêUTICOS"<D>. Composto da fórmula I: em que Y é O ou S; Ar é um grupo arila ou um grupo heteroarila; R é H, um grupo alquila, um grupo cicloalquila, um grupo heterocicloalquila, um grupo arila, um grupo heteroarila, ou -C(O)R~ 1~, em que R~ 1~ é hidrogênio, um grupo alquila, um grupo cicloalquila, um grupo heterocicloalquila, um grupo arila, um grupo heteroarila ou NR~ 2~R~ 3~, em que R~ 2~ e R~ 3~ são independentemente hidrogênio, um grupo alquila, um grupo cicloalquila, um grupo heterocicloalquila, um grupo arila, ou um grupo heteroarila; e X é -NH-OH ou -OH. Pró-drogas, sais e solvatos farmaceuticamente aceitáveis desses compostos. Métodos de inibição da atividade das metaloproteinases através da administração de um composto da fórmula I ou uma pró-droga, sal ou solvato farmaceuticamente aceitável do mesmo. Composições farmacêuticas compreendendo uma quantidade efetiva desses compostos, pró-drogas, sais e solvatos.Invention Patent: <B> "METHALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AND THEIR PHARMACEUTICAL USES" <D>. Compound of formula I: where Y is O or S; Ar is an aryl group or a heteroaryl group; R is H, an alkyl group, a cycloalkyl group, a heterocycloalkyl group, an aryl group, a heteroaryl group, or -C (O) R ~ 1 ~, where R ~ 1 ~ is hydrogen, an alkyl group, a group cycloalkyl, a heterocycloalkyl group, an aryl group, a heteroaryl group or NR ~ 2 ~ R ~ 3 ~, where R ~ 2 ~ and R ~ 3 ~ are independently hydrogen, an alkyl group, a cycloalkyl group, a heterocycloalkyl group, an aryl group, or a heteroaryl group; and X is -NH-OH or -OH. Pharmaceutically acceptable prodrugs, salts and solvates of these compounds. Methods of inhibiting the activity of metalloproteinases by administering a compound of formula I or a pharmaceutically acceptable prodrug, salt or solvate thereof. Pharmaceutical compositions comprising an effective amount of these compounds, prodrugs, salts and solvates.

BR9809062-3A 1997-04-01 1998-03-31 Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses BR9809062A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US82531897A 1997-04-01 1997-04-01
PCT/US1998/006365 WO1998043963A1 (en) 1997-04-01 1998-03-31 Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses

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BR9809062A true BR9809062A (en) 2000-08-01

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BR9809062-3A BR9809062A (en) 1997-04-01 1998-03-31 Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses

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EP (1) EP0973748A1 (en)
JP (1) JP2001521504A (en)
KR (1) KR20010005940A (en)
AU (1) AU747280B2 (en)
BR (1) BR9809062A (en)
CA (1) CA2285372A1 (en)
NZ (1) NZ338082A (en)
WO (1) WO1998043963A1 (en)

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WO1998043963A1 (en) 1998-10-08
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KR20010005940A (en) 2001-01-15

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