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BR9814643A - Inibidor de metaloprotease de ácido sulfona hidroxâmico aromático - Google Patents

Inibidor de metaloprotease de ácido sulfona hidroxâmico aromático

Info

Publication number
BR9814643A
BR9814643A BR9814643-2A BR9814643A BR9814643A BR 9814643 A BR9814643 A BR 9814643A BR 9814643 A BR9814643 A BR 9814643A BR 9814643 A BR9814643 A BR 9814643A
Authority
BR
Brazil
Prior art keywords
mmp
inhibitor
aromatic hydroxamic
hydroxamic acid
optionally substituted
Prior art date
Application number
BR9814643-2A
Other languages
English (en)
Inventor
Thomas E Barta
Daniel P Becker
Terri L Boehm
Gary A De Crescenzo
Clara I Villamil
Joseph J Mcdonald
John N Freskos
Daniel P Getman
Original Assignee
Searle & Co
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 Searle & Co filed Critical Searle & Co
Publication of BR9814643A publication Critical patent/BR9814643A/pt

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/426—1,3-Thiazoles
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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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    • C07D211/60—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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    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
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    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

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Abstract

Patente de Invenção: <B>"INIBIDOR DE METALOPROTEASE DE áCIDO SULFONA HIDROXâMICO AROMáTICO"<D>. Um processo de tratamento é descrevedo, que compreende administrar uma quantidade efetiva de um ácido sulfona hidroxâmico aromático, que exibe excelente atividade inibitória de uma ou mais enzimas de metaloprotease de matriz (MMP), tais como a MMP-2, a MMP-9 e a MMP-13, ao mesmo tempo que exibe substancialmente menos inibição pelo menos da MMP-1, a um hospedeiro tendo uma condição associada com atividade da metaloprotease de matriz patológica. O inibidor de enzima administrado corresponde, na estrutura, à fórmula (I), abaixo descrita, ou a um sal farmaceuticamente aceitável do mesmo, na qual R¹ e R² são ambos hidrido, ou R¹ e R², juntos com os átomos aos quais eles estão ligados, formam um anel com 5 a 8 elementos, contendo um, dois ou três heteroátomos no anel, que são o oxigênio, o enxofre ou o nitrogênio. R³ na fórmula (I) é um radical arila opcionalmente substituída ou heteroarila opcionalmente substituída. Também descrevedos são os compostos inibidores de metaloprotease tendo estas atividades seletivas, os processos para a manufatura de tais compostos e as composições farmacêuticas que utilizam um inibidor.
BR9814643-2A 1997-11-14 1998-11-12 Inibidor de metaloprotease de ácido sulfona hidroxâmico aromático BR9814643A (pt)

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PCT/US1998/023242 WO1999025687A1 (en) 1997-11-14 1998-11-12 Aromatic sulfone hydroxamic acid metalloprotease inhibitor

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CN1279669A (zh) 2001-01-10
AU756150C (en) 2004-03-04
ZA9810412B (en) 1999-12-09
PL341379A1 (en) 2001-04-09
WO1999025687A1 (en) 1999-05-27
AR016010A1 (es) 2001-05-30
EP1042290A1 (en) 2000-10-11
NZ503485A (en) 2002-10-25
JP2001523662A (ja) 2001-11-27
NO20002469L (no) 2000-07-12
US20060084688A1 (en) 2006-04-20
IL135106A0 (en) 2001-05-20
CA2306460A1 (en) 1999-05-27
AU1373299A (en) 1999-06-07
US6890937B2 (en) 2005-05-10
NO20002469D0 (no) 2000-05-12
RU2250105C2 (ru) 2005-04-20
US20040048852A1 (en) 2004-03-11
US6541489B1 (en) 2003-04-01
AU756150B2 (en) 2003-01-02

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