发明申请
US20040214812A1 4-Substituted or unsubstituted-7-hydro-1,4-thiazepine-7-[bicyclic or tricyclic heteroaryl] substituted-3,6-dicarboxylic acid derivatives as beta-lactamase inhibitors 失效
4-取代或未取代的7-氢-1,4-硫杂氮杂-7- [双环或三环杂芳基]取代-3,6-二羧酸衍生物作为β-内酰胺酶抑制剂

4-Substituted or unsubstituted-7-hydro-1,4-thiazepine-7-[bicyclic or tricyclic heteroaryl] substituted-3,6-dicarboxylic acid derivatives as beta-lactamase inhibitors
摘要:
The present invention relates to novel, low molecular weight broad spectrum compounds in particular to a class of 4-substituted or unsubstituted-7-hydro-1,4-thiazepine-7-nullbicyclic or tricyclic heteroarylnull substituted-3,6-dicarboxylic acid or their derivatives which have null-lactamase inhibitory and antibacterial properties. The compounds are therefore useful in the treatment of antibacterial infections in humans or animals, either alone or in combination with other antibiotics.
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