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US 10,864,273 B2Granted
Thiobase compounds for photodynamic therapy
AssigneeCase Western Reserve University
InventorsCarlos E. Crespo-Hernandez, Marvin Pollum
Life of this patent
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Abstract
A method of using a compound in a phototherapy procedure includes administering to a subject in need of treatment a therapeutically effective amount of a thio-substituted nucleobase, nucleoside, nucleotide, and/or analogs thereof; and exposing the administered compound to electromagnetic radiation.
Claims17
A method of using a compound in a phototherapy procedure, the method comprising:
- administering to a subject in need of treatment a therapeutically effective amount of compound having the formula:
- or pharmaceutically acceptable salts thereof;
- wherein R1 is H, OH, ribose, deoxyribose, amino acid residue(s), fatty acid residue(s), ORa, where Ra comprises at least one of a straight chain, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, arylsulfonyl, or aralkylsulfonyl, or a mono, di, or triphosphate thereof,
- R2 and R3 are independently the same or different and are each selected from the group consisting of a H, F, Cl, Br, I, a lower alkyl group, (CH2)n1OR′ (wherein n1=1, 2, or 3), CF3, CH2—CH2X, O—CH2—CH2X, CH2—CH2—CH2X, O—CH2—CH2X (wherein X═F, Cl, Br, or I), CN, (C═O)—R′, N(R′)2, NO2, (C═O)N(R′)2, O(CO)R′, OR′, SR′, COOR′ (wherein R′ is H or a lower alkyl group), or a substituted or unsubstituted aryl, heteroaryl, cycloalkyl, or heterocyclyl, and wherein R2 and R3 if present may be linked to form a cyclic or polycyclic ring, wherein the ring is a substituted or unsubstituted aryl, heteroaryl, cycloalkyl, or heterocyclyl;
- and
- exposing the administered compound to electromagnetic radiation.
3 more elements
A method of treating cancer or a cancer-associated disorder in a subject in need thereof, the method comprising:
- administering to a subject in need of treatment a therapeutically effective amount of compound having the formula:
- or pharmaceutically acceptable salts thereof;
- wherein R1 is H, OH, ribose, deoxyribose, amino acid residue(s), fatty acid residue(s), ORa, where Ra comprises at least one of a straight chain, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, arylsulfonyl, or aralkylsulfonyl, or a mono, di, or triphosphate thereof,
- R2 and R3 are independently the same or different and are each selected from the group consisting of a H, F, Cl, Br, I, a lower alkyl group, (CH2)n1OR′ (wherein n1=1, 2, or 3), CF3, CH2—CH2X, O—CH2—CH2X, CH2—CH2—CH2X, O—CH2—CH2X (wherein X═F, Cl, Br, or I), CN, (C═O)—R′, N(R′)2, NO2, (C═O)N(R′)2, O(CO)R′, OR′, SR′, COOR′ (wherein R′ is H or a lower alkyl group), or a substituted or unsubstituted aryl, heteroaryl, cycloalkyl, or heterocyclyl, and wherein R2 and R3 if present may be linked to form a cyclic or polycyclic ring, wherein the ring is a substituted or unsubstituted aryl, heteroaryl, cycloalkyl, or a heterocyclyl;
- and
- exposing the administered compound to electromagnetic radiation effective to treat the cancer or cancer-associated disorder.
3 more elements
Dependencies are inferred from the claim text.