Amelioration of the development of cataracts and other ophthalmic diseases
AssigneeOthera Holding, Inc.
InventorsWilliam L. Matier, Ghanshyam Patil
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AssigneeOthera Holding, Inc.
InventorsWilliam L. Matier, Ghanshyam Patil
Estimating the term…
Ophthalmically acceptable compositions used in arresting the development of cataracts or macular degeneration comprising a pharmaceutically acceptable carrier or diluent and a compound having the formula: 1 where R1 and R2 are, independently, H or C1 to C3 alkyl; R3 and R4 are, independently C1 to C3 alkyl; and where R1 and R2, taken together, or R3 and R4, taken together, or both may be cycloalkyl; R5 is H, OH, or C1 to C6 alkyl; R6 is or C1 to C6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl; R7 is C1 to C6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl or where R6 and R7, or R5, R6 and R7, taken together, form a carbocycle or heterocycle having from 3 to 7 atoms in the ring.
A composition comprising a pharmaceutically acceptable carrier or diluent and a compound having the formula:
An opthalmic composition comprising an opthalmically acceptable carrier or diluent and a compound having an N-hydroxy piperidine portion bound to a solubility modifying portion, the compound having a solubility in water at 25° C. of at least about 0.25% by weight and a water—n-octonal partition coefficient at 25° C. of at least about 5.
A method of administering an antioxidant to a mammal comprising contacting the mammal with a composition comprising a pharmaceutically acceptable carrier or diluent and a compound having an N-hydroxy piperidine portion bound to a solubility modifying portion, the compound having a solubility in water at 25° C. of at least about 0.25% by weight and a water—n-octonal partition coefficient at 25° C. of at least about 5.
A method for identifying a pharmaceutical for delivery to the eye of a patient in the form of eye drops comprising selecting a compound having a water solubility at 25° C. of at least about 0.25% by weight and a water—n-octonal partition coefficient of at least about 5 at 25° C., which compound is enzymatically cleavable under conditions obtained in the lens of the eye of a patient to give rise to an N-hydroxy piperidine.
A method of administering an antioxidant to a mammal comprising contacting the mammal with a composition comprising a pharmaceutically acceptable carrier or diluent with a compound having the formula:
A method of ameliorating the development of a cataract in the eye of a patient comprising administering to the eye of such patient an ophthalmic composition comprising an ophthalmically acceptable carrier or diluent containing a compound having the formula:
A method of ameliorating the development of a cataract in the eye of a patient comprising administering to the eye of such patient an ophthalmic composition comprising an ophthalmically acceptable carrier or diluent and a compound having an N-hydroxy piperidine portion bound to a solubility modifying portion, the compound having a solubility in water at 25° C. of at least about 0.25% by weight and a water—n-octonal partition coefficient at 25° C. of at least about 5.
A method of treating macular degeneration in the lens of a patient comprising administering to the eye of such patient an ophthalmologic composition comprising an ophthalmically acceptable carrier or diluent in the form of eye drops containing a compound having the formula:
Dependencies are inferred from the claim text.