Compositions and methods with enhanced therapeutic activity
View Patent ↗Novel quinone and catechol compositions, compositions containing prodrugs of quinone and catechol compositions, and methods of use for the treatment of solid tumor cancers and other vascular proliferative disorders. The disclosure particularly relates to the discovery of dual activity agents capable of generating both a vascular targeting effect and direct tumor cell cytotoxicity in order to achieve an enhanced anti-tumor response in a patient.
1. A composition of the following formula (V):
wherein
a. Z is an ethylene (—CH═CH—) bridge in the cis (Z) isomeric configuration;
b. R 1 and R 2 are OH or a prodrug form thereof;
c. R 3 is selected from the group consisting of
i) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight-chain lower alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, or lower alkanoyloxy;
ii) a halogen or trihaloalkyl;
iii) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight chain lower alkyl, allyl, allyloxy, vinyl, or vinyloxy;
iv) a C 1 , C 2 , C 3 , C 4 or C 5 primary, secondary, or tertiary alcohol; and
v) oxo, lower alkanoyl, thio, sulfonyl, sulfonamide, nitro, nitrosyl, cyano, carboxy, carbamyl, aryl, or heterocycle;
d. R 4 , R 5 , and R 9 are hydrogen,
e. R 6 and R 8 are the same or different and selected from the group consisting of hydrogen and
i) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight-chain lower alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, or lower alkanoyloxy;
ii) a halogen or trihaloalkyl;
iii) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight chain lower alkyl, allyl, allyloxy, vinyl, or vinyloxy; or
iv) a C 1 , C 2 , C 3 , C 4 or C 5 primary, secondary, or tertiary alcohol; and
v) nitro;
f. R 7 , is selected from the group consisting of
i) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight-chain lower alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, or lower alkanoyloxy;
ii) a halogen or trihaloalkyl;
iii) a C 1 , C 2 , C 3 , C 4 or C 5 branched or straight chain lower alkyl, allyl, allyloxy, vinyl, or vinyloxy;
iv) a C 1 , C 2 , C 3 , C 4 or C 5 primary, secondary, or tertiary alcohol; and
v) nitro;
provided that said compound is not combretastatin A1 or prodrug thereof.
2. The composition of claim 1 , wherein R 6 , R 7 , and R 8 are not hydrogen.
3. The composition of claim 2 , wherein R 6 , R 7 and R 8 are the same.
4. The composition of claim 3 , wherein R 6 , R 7 and R 8 are methoxy.
5. The composition of claim 4 , wherein R 3 is —CH 3 , —CH 2 CH 3 , —OCH 2 CH 3 , —F, —Br, —CF 3 , —CBr 3 , —O—CH 2 —CH═CH 2 , —CH 2 —CH═CH 2 , —NO 2 , -cyano, or -carboxy.
6. The composition of claim 3 , wherein R 6 , R 7 , and R 8 are F.
7. The composition of claim 6 , wherein R 3 is —CH 3 , —CH 2 CH 3 , —OCH 2 CH 3 , —F, —Br, —CF 3 , —CBr 3 , —O—CH 2 —CH═CH 2 , —CH 2 —CH═CH 2 , —NO 2 , -cyano, -carboxy, or -benzyl.
8. A composition selected from the group consisting of
3-Ethyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
3-Methyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
4-Bromo-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
4-Phenyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
3-Allyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
4-Fluoro-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-dihydroxybenzene,
2,3,4-Trihydroxy-6-[(Z)-2(3,4,5-trimethoxyphenyl)vinyl]-benzene,
2,3-Dihydroxy-4-ethoxy-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-benzene,
2,3-Dihydroxy-4-allyloxy-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-benzene,
4-Nitro-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-2,3-dihydroxybenzene,
2′,3′ dihydroxy-3,5 dichloro-4,4′-dimethoxy-(Z)-stilbene,
2′,3′ dihydroxy-4′-methoxy-3,4,5-trifluoro-(Z)stilbene,
2,3-Dihydroxy-4-methoxy-[(Z)-2-(3,4,5-trimethoxyphenyl) Beta-lactam]-benzene,
2′,3′ diphosphate-3,4,5-trimethoxy-(Z)-stilbene, tetrasodium salt;
3′,4′ diphosphate-3,4,5-trimethoxy-(Z)-stilbene, tetrasodium salt;
and combinations thereof.