Therapeutic use of riboside of 5-aminoimidazole-4-carboxamide (acadesine)
View Patent ↗The present disclosure relates to a method of treatment of a human patient suffering from a B-cell lymphoproliferative disorders such as B-cell chronic lymphocytic leukemia (B-CLL), splenic marginal zone lymphoma (SMZL), mantle cell lymphoma (MCL), follicular lymphoma (FL), lymphoplasmacytic lymphoma (LPL), and Waldenström syndrome (WS), by the administration of a therapeutically effective amount of 5-aminoimidazole-4-carboxamide riboside (acadesine) or its precursors (eg. its mono-, di- and tri-5′-phosphates). This makes acadesine and its bioprecursors (eg. its mono-, di- and tri-5′-phosphates) useful as therapeutic agents for B-cell lymphoproliferative disorders in humans. The surprising feature that T cells are virtually not affected means that the side effect (immunosuppression) is minor, what represents a therapeutical advantage of acadesine over cladribine, fludarabine and other nucleosides known in the art.
1. A method of treatment of a human patient suffering from a B-cell lymphoproliferative disorder, comprising administering a therapeutically effective amount of a compound of formula (I), or a pharmaceutically acceptable solvate or addition salt thereof, together with appropriate amounts of pharmaceutically acceptable diluents or carriers; wherein, —R 2 , —R 3 and —R 5 are radicals independently selected from the group consisting of —H, PO(OH) 2 , PO(OH)—O—PO(OH) 2 , PO(OH)—O—PO(OH)—O—PO(OH) 2 , CO—R′ and CO—OR′; R′ being a hydrocarbyl radical up to twelve carbon atoms, which may be aliphatic including alkyl, alkenyl, and alkynyl groups and groups which have a mixture of saturated and unsaturated bonds, alicyclic, aryl or a combination thereof; wherein R′ may be a radical from a straight-chain, a branched-chain, a cycle or a combination thereof; —R′ may have one or more hydrogen atoms substituted by one or more halogen atoms, and/or by one or more (C 1 -C 4 )-alkyl groups; R′ may have one or more CH 2 groups substituted by one or more NH, O and/or S groups; and R′ may have one or more CH groups substituted by one or more N atoms
2. The method according to claim 1 , wherein in the compound of formula (I) —R 2 , —R 3 and —R 5 are radicals independently selected from the group consisting of H, PO(OH) 2 , PO(OH)—O—PO(OH) 2 and PO(OH)—O—PO(OH)—O—PO(OH) 2 .
3. The method according to claim 2 , wherein in the compound of formula (I) —R 2 and —R 3 are radicals H, and —R 5 is a radical selected from the group consisting of H and —PO(OH) 2 .
4. The method according to claim 3 , wherein in the compound of formula (I) —R 2 , —R 3 and —R 5 are radicals H.
5. The method according to any of the claims 3 to 4 , wherein the B-cell lymphoproliferative disorder is B-cell chronic lymphocytic leukemia.
6. The method according to any of the claims 1 to 4 , wherein the B-cell lymphoproliferative disorder is splenic marginal zone lymphoma.
7. The method according to any of the claims 1 to 4 , wherein the B-cell lymphoproliferative disorder is mantle cell lymphoma.
8. The method according to any of the claims 1 to 4 , wherein the B-cell lymphoproliferative disorder is follicular lymphoma.
9. The method according to any of the claims 1 to 4 , wherein the B-cell lymphoproliferative disorder is lymphoplasmacytic lymphoma.
10. The method according to any of the claims 1 to 4 , wherein the B-cell lymphoproliferative disorder is Waldenström syndrome.