FIELD: organic chemistry, medicine, pharmacy.
SUBSTANCE: invention relates to new derivatives of chromenone and chromanone taken among the group including the following compounds: (2S)-3-{2-[3-(1H-imidazol-2-ylamino)propyl]-4-oxo-4H-chromen-6-yl}-2-(2,2-dimethylpropoxycarboxamido)propionic acid ethyl ester; (2S)-3-{2-[3-(1H-imidazol-2-ylamino)propyl]-4-oxo-4H-chromen-6-yl}-2-(2,2-dimethylpropoxycarboxamido)propionic acid; (2S)-3-{2-[3-pyridin-2-ylamino)propyl]-4-oxo-4H-chromen-6-yl}-2-(2,2-dimethylpropoxycarboxamido)propionic acid; (2S)-3-{2-[3-(pyridin-2-ylamino)propyl]-4-oxo-4H-chromen-6-yl}-2-butylsulfonamidopropionic acid; (2S)-3-{2-[3-pyridin-2-ylamino)propyl]-4-oxo-4H-4H-chromen-6-yl}-2-benzylsulfonamidepropionic acid and their physiologically acceptable salts, enantiomers or diastereomers also. These compounds are inhibitors of αvβ3-integrins used for control of angiogenic diseases caused by pathological factors, namely: thrombosis, myocardium infarction, heart ischemic disease, artheriosclerosis, tumors, osteoporosis and rheumatic arthritis. Invention relates also to pharmaceutical composition based on these compounds and to method for its preparing.
EFFECT: improved preparing method, valuable medicinal properties of compounds and composition.
5 cl, 2 tbl, 17 ex
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Authors
Dates
2004-08-20—Published
1999-10-14—Filed