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US 6,281,250 B1Granted
Retinyl ethers, derivatives and analogues and inhibition of breast carcinogenesis
AssigneeSouthern Research Institute
InventorY. Fulmer Shealy
Life of this patent
Estimating the term…
Abstract
The present invention is directed to retinyl ethers, derivatives and analogues and their use in inhibiting breast carcinogenesis or breast cancer cell growth.
Claims16
A compound having the general formula
- X—O—(CRR1)n—Y (I)
- wherein R and R1 are independently H, OH, halogen, C1-C10-alkyl, C1-C10-alkyl halide, C1-C10-alkoxy, phenoxy or an aryl group;
- n is 0 or 1;
- Y is an unsubstituted or substituted aryl;
- and X is a structure selected from the group consisting of
- wherein R2 is H, OH or ═O, R3 is CH3 or CH2OH, and R9 is H, or C1-C5 alkyl, or a physiologically acceptable salt thereof, with the provisos that (1) when R and R1 are both H, X is structure (a), R2 is H, R3 is CH3 and n is 1, then Y is not trimethoxyphenyl or 4-ethynlphenyl;
- (2) when R2 is H, R3 is CH3 X is structure (a) and n is 0, then Y is not 4-methoxyphenyl;
- (3) when R and R1 are both H, X is structure (a), R2 is H, R3 is CH3 and n is 1, then Y is not phenyl;
- and (4) when X is structure (a), n is 1 and Y is phenyl, then both R and R1 are not phenyl.
6 more elements
A method of inhibiting breast cancer in an individual which comprises administering to the individual an effective amount of a compound having the general formula
- X—O—(CRR1)n—Y (I)
- wherein R and R1 are independently H, OH, halogen, C1-C10-alkyl, C1-C10-alkyl halide, C1-C10-alkoxy, phenoxy or an aryl group;
- n is 0 or 1;
- Y is an unsubstituted or substituted aryl;
- and X is a stricture selected from the group consisting of
- wherein R2 is H, OH or ═O, R3 is CH3 or CH2OH, and R9 is H, or C1-C5 alkyl, or a physiologically acceptable salt thereof.
3 more elements
Dependencies are inferred from the claim text.