Metalloproteinase inhibitors, pharmaceutical compositions...

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 213/70 (2006.01) A61K 31/495 (2006.01) A61K 31/535 (2006.01) A61K 31/54 (2006.01) C07C 309/87 (2006.01) C07D 213/68 (2006.01) C07D 239/10 (2006.01) C07D 241/04 (2006.01) C07D 265/30 (2006.01) C07D 279/12 (2006.01) C07D 401/12 (2006.01) C07D 403/12 (2006.01) C07D 405/12 (2006.01) C07D 413/12 (2006.01) C07D 417/12 (2006.01) C07F 7/10 (2006.01)

Patent

CA 2238306

The invention relates to compounds of formula (1) wherein: Z is O or S; V is a divalent radical which together with C* and N forms a ring having six ring atoms, where each of said ring atoms other than C* and N independently is unsubstituted or substituted by a suitable substituent, and at least one of said other ring atoms is a heteroatom selected from O, N and S, and the remainder is carbon atoms; and Ar is an aryl or heteroaryl group; and pharmaceutically acceptable prodrugs, salts and solvates thereof. The invention further relates to pharmaceutically acceptable prodrugs, salts and solvates of these compounds. The invention also relates to methods of inhibiting the activity of metalloproteinases by administering a compound of formula (1) or a prodrug, salt or solvate thereof. The invention further relates to pharmaceutical compositions comprising an effective amount of these compounds, prodrugs, salts, and solvates. The invention still further relates to methods and intermediates useful for preparing these compounds, prodrugs, salts, and solvates.

Cette invention se rapporte à des composés représentés par la formule (1), dans laquelle: Z représente O ou S; V représente un radical divalent qui, avec C* et N, forme un cycle ayant 6 atomes cycliques, où chacun de ces atomes cycliques autres que C* et N indépendamment est insubstitué ou substitué par un substituant approprié, et au moins l'un de ces autres atomes cycliques est un hétéroatome choisi parmi O, N et S, et les atomes restants sont des atomes de carbone; et Ar représente un groupe aryle ou hétéroaryle. Cette invention se rapporte en outre à des promédicaments, des sels et des solvates de ces composés, qui sont acceptables sur le plan pharmaceutique. Cette invention se rapporte également à des procédés pour inhiber l'activité de métalloprotéinases, en administrant un composé représenté par la formule (1) ou un promédicament, sel ou solvate de ce composé. Cette invention se rapporte en outre à des compositions pharmaceutiques comprenant une quantité efficace de ces composés, promédicaments, sels et solvates. Cette invention se rapporte enfin à des procédés et à des intermédiaires servant à préparer ces composés, promédicaments, sels, et solvates.

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