METHODS AND COMPOSITIONS FOR ENHANCING LIFESPAN INVOLVING SIRTUIN-MODULATING COMPOUNDS AND CHALCOGENIDES
The present invention concerns the use of active compounds, including chalcogenides and sirtuin-modulating compounds, either alone or in combination for increasing or enhancing survivability and/or longevity in biological matter. In general aspects, the chalcogenides and other active compounds may modulate one or more sirtuin proteins. It includes compositions, methods, articles of manufacture and apparatuses for enhancing survivability in any of these biological materials, so as to preserve and/or protect them. In specific embodiments, there are also therapeutic methods and apparatuses for aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, organ transplantation, hyperthermia, wound healing, hemorrhagic shock, cardioplegia for bypass surgery, neurodegeneration, hypothermia, and cancer using the active compounds described.
1 .- 2 . (canceled)
3 . A method of enhancing lifespan in biological matter comprising administering to the biological matter a sirtuin-modulating compound in combination with a chalcogenide.
4 . The method of claim 3 , wherein the biological matter comprises cells.
5 .- 7 . (canceled)
8 . The method of claim 3 , wherein the chalcogenide is sulfide.
9 . The method of claim 3 , wherein the sirtuin-modulating compound is selected from the group comprising formula 1-188.
10 . The method of claim 3 , wherein the sirtuin-modulating compound is selected from the group consisting of nicotinic acid, resveratrol, butein, fisetin, piceatannol, isoliquiritigenin and quercetin.
11 . (canceled)
12 . A method for enhancing lifespan in biological matter comprising providing to the biological matter a chalcogenide of formula (I) or (IV) or salt or prodrug thereof, wherein formula (I) and (IV) comprise:
wherein X is N, O, Po, S, Se, or Te;
wherein Y is N or O;
wherein R 1 is H, C, lower alkyl, a lower alcohol, or CN;
wherein R 2 is H, C, lower alkyl, or a lower alcohol, or CN;
wherein n is 0 or 1;
wherein m is 0 or 1;
wherein k is 0, 1, 2, 3, or 4; and,
wherein p is 1 or 2;
wherein:
X is N, O, P, Po, S, Se, Te, O—O, Po—Po, S—S, Se—Se, or Te—Te;
n and m are independently 0 or 1;
R 21 and R 22 are independently hydrogen, halo, cyano, phosphate, thio, alkyl, alkenyl, alkynyl, alkoxy, aminoalkyl, cyanoalkyl, hydroxyalkyl, haloalkyl, hydroxyhaloalkyl, alkylsulfonic acid, thiosulfonic acid, alkylthiosulfonic acid, thioalkyl, alkylthio, alkylthioalkyl, alkylaryl, carbonyl, alkylcarbonyl, haloalkylcarbonyl, alkylthiocarbonyl, aminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, haloalkylcarbonyl, alkoxycarbonyl, aminoalkylthio, hydroxyalkylthio, cycloalkyl, cycloalkenyl, aryl, aryloxy, heteroaryloxy, heterocyclyl, heterocyclyloxy, sulfonic acid, sulfonic alkyl ester, thiosulfate, or sulfonamido; and
Y is cyano, isocyano, amino, alkyl amino, aminocarbonyl, aminocarbonyl alkyl, alkylcarbonylamino, amidino, guanidine, hydrazino, hydrazide, hydroxyl, alkoxy, aryloxy, hetroaryloxy, cyloalkyloxy, carbonyloxy, alkylcarbonyloxy, haloakylcarbonyloxy, arylcarbonyloxy, carbonylperoxy, alkylcarbonylperoxy, arylcarbonylperoxy, phosphate, alkylphosphate esters, sulfonic acid, sulfonic alkyl ester, thiosulfate, thiosulfenyl, sulfonamide, —R 23 R 24 , wherein R 23 is S, SS, Po, Po—Po, Se, Se—Se, Te, or Te—Te, and R 24 is defined as for R 21 herein, or Y is
wherein X, R 21 and R 22 , are as defined herein.
13 . The method of claim 12 , wherein X is sulfur.
14 . The method of claim 12 , wherein the chalcogenide is a sulfide salt.
15 . The method of claim 14 , wherein the salt is a sulfide salt selected from the group consisting of sodium sulfide (Na 2 S), sodium hydrogen sulfide (NaHS), potassium sulfide (K 2 S), potassium hydrogen sulfide (KHS), lithium sulfide (Li 2 S), rubidium sulfide (Rb 2 S), cesium sulfide (Cs 2 S), ammonium sulfide ((NH 4 ) 2 S), ammonium hydrogen sulfide (NH 4 )HS, beryllium sulfide (BeS), magnesium sulfide (MgS), calcium sulfide (CaS), strontium sulfide (SrS) and barium sulfide (BaS).
16 . The method of claim 12 , wherein the chalcogenide is selected from the group consisting of H2S, H2Se, H 2 Te and H 2 Po.
17 .- 38 . (canceled)
39 . A method for enhancing survivability of biological matter comprising administering to the matter an effective amount of a composition having one or more compounds with formula (I) and/or formula (IV), or a salt or prodrug thereof, in combination with a sirtuin-modulating compound.
40 .- 42 . (canceled)
43 . A method for extending longevity to biological matter under adverse conditions comprising administering to the biological matter an effective amount of a chalcogenide in combination with a sirtuin-modulating compound, wherein damage is prevented or reduced.
44 . The method of claim 43 , wherein the biological matter is treated with the combination of an active compound and the sirtuin-modulating compound.
45 . The method of claim 44 , wherein the active compound is sulfide.
46 . (canceled)
47 . A method of preventing an organism from bleeding to death comprising providing to the bleeding organism an effective amount of a chalcogenide in combination with a sirtuin-modulating compound to prevent death.
48 . The method of claim 47 , wherein the organism goes into hemorrhagic shock.
49 . The method of claim 47 , wherein the chalcogenide is a sulfur-containing compound.
50 . The method of claim 47 , wherein the chalcogenide is formula (I) or a salt or prodrug thereof, wherein formula (I) comprises
wherein X is S;
wherein k is 0
wherein m is 0;
wherein n is 0 or 1; and
wherein R 1 is H.
51 .- 58 . (canceled)
59 . A method of modulating sirtuin activity in biological matter comprising providing the biological matter with a chalcogenide of formula (I) or (IV) or salt or prodrug thereof, wherein formula (I) and (IV) comprise:
wherein X is N, O, Po, S, Se, or Te;
wherein Y is N or O;
wherein R 1 is H, C, lower alkyl, a lower alcohol, or CN;
wherein R 2 is H, C, lower alkyl, or a lower alcohol, or CN;
wherein n is 0 or 1;
wherein m is 0 or 1;
wherein k is 0, 1, 2, 3, or 4; and,
wherein p is 1 or 2;
wherein:
X is N, O, P, Po, S, Se, Te, O—O, Po—Po, S—S, Se—Se, or Te—Te;
n and m are independently 0 or 1;
R 21 and R 22 are independently hydrogen, halo, cyano, phosphate, thio, alkyl, alkenyl, alkynyl, alkoxy, aminoalkyl, cyanoalkyl, hydroxyalkyl, haloalkyl, hydroxyhaloalkyl, alkylsulfonic acid, thiosulfonic acid, alkylthiosulfonic acid, thioalkyl, alkylthio, alkylthioalkyl, alkylaryl, carbonyl, alkylcarbonyl, haloalkylcarbonyl, alkylthiocarbonyl, aminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, haloalkylcarbonyl, alkoxycarbonyl, aminoalkylthio, hydroxyalkylthio, cycloalkyl, cycloalkenyl, aryl, aryloxy, heteroaryloxy, heterocyclyl, heterocyclyloxy, sulfonic acid, sulfonic alkyl ester, thiosulfate, or sulfonamido; and
Y is cyano, isocyano, amino, alkyl amino, aminocarbonyl, aminocarbonyl alkyl, alkylcarbonylamino, amidino, guanidine, hydrazino, hydrazide, hydroxyl, alkoxy, aryloxy, hetroaryloxy, cyloalkyloxy, carbonyloxy, alkylcarbonyloxy, haloakylcarbonyloxy, arylcarbonyloxy, carbonylperoxy, alkylcarbonylperoxy, arylcarbonylperoxy, phosphate, alkylphosphate esters, sulfonic acid, sulfonic alkyl ester, thiosulfate, thiosulfenyl, sulfonamide, —R 23 R 24 , wherein R 23 is S, SS, Po, Po—Po, Se, Se—Se, Te, or Te—Te, and R 24 is defined as for R 21 herein, or Y is
wherein X, R 21 and R 22 , are as defined herein.
60 . The method of claim 59 , further comprising providing the biological matter with a sirtuin-modulating compound.
61 . The method of claim 59 , wherein X is sulfur.
62 . The method of claim 59 , wherein the chalcogenide is a sulfide salt.
63 . The method of claim 62 , wherein the salt is a sulfide salt selected from the group consisting of sodium sulfide (Na 2 S), sodium hydrogen sulfide (NaHS), potassium sulfide (K 2 S), potassium hydrogen sulfide (KHS), lithium sulfide (Li 2 S), rubidium sulfide (Rb 2 S), cesium sulfide (Cs 2 S), ammonium sulfide ((NH 4 ) 2 S), ammonium hydrogen sulfide (NH 4 )HS, beryllium sulfide (BeS), magnesium sulfide (MgS), calcium sulfide (CaS), strontium sulfide (SrS) and barium sulfide (BaS).
64 . The method of claim 59 , wherein the chalcogenide is selected from the group consisting of H2S, H2Se, H 2 Te and H 2 Po.