Nicotinoyl riboside compositions and methods of use

Patent metadata

Field	Value
Publication number	US-9321797-B2
Application number	US-201414543439-A
Country	US
Kind code	B2
Filing date	Nov 17, 2014
Priority date	Nov 18, 2005
Publication date	Apr 26, 2016
Grant date	Apr 26, 2016

Abstract

The invention relates to compositions of nicotinoyl ribosides and nicotinamide riboside derivatives and their methods of use. In some embodiments, the invention relates to methods of making nicotinoyl ribosides. In some embodiments, the invention relates to pharmaceutical compositions and nutritional supplements containing a nicotinoyl riboside. In further embodiments, the invention relates to methods of using nicotinoyl ribosides and nicotinamide riboside derivatives that promote the increase of intracellular levels of nicotinamide adenine dinucleotide (NAD+) in cells and tissues for improving cell and tissue survival.

First claim

The invention claimed is:

1. A method of reducing toxicity induced by a HMGCoA reductase inhibitor in a mammal, which method comprises administering to the mammal a therapeutically effective amount of a compound of formula (I):

and salt complexes thereof, wherein R is selected from the group consisting of amino, alkylamino, substituted alkylamino, dialkylamino, substituted dialkylamino, alkyloxy, substituted alkyloxy, aryloxy, substituted aryloxy, hydroxylamino, substituted hydroxylamino, O-alkyloxyamino, substituted O-alkyloxyamino, aminooxy, substituted aminoxy, N-alkylaminooxy, substituted N-alkylaminoxy, hydrazino, substituted hydrazino, alkylhydrazino, and substituted alkylhydrazino,
wherein the mammal has been administered the HMGCoA reductase inhibitor in an amount that produces toxicity in the mammal in the absence of the administration of the compound of formula (I), and
wherein the administration of the compound of formula (I) reduces the toxicity in the mammal.

2. The method of claim 1 , wherein the alkyloxy or substituted alkyloxy is selected from —OMe, —OEt, and —OCH 2 CH 2 OH.

3. The method of claim 1 , wherein the aryloxy is —OPh.

4. The method of claim 1 , wherein the alkylamino or substituted alkylamino is selected from —NHMe, —NHEt, —NHCH 2 CH 2 OH, —NHCH 2 CH═CH 2 , —NHCH(CH 3 ) 2 , —NHCH 2 CH 2 NH 2 , and —NHcyclopropyl.

5. The method of claim 1 , wherein the dialkylamino is —N(CH 3 ) 2 or N-substituted pyrrolidinyl.

6. The method of claim 1 , wherein the HMGCoA reductase inhibitor is a statin.

7. The method of claim 6 , wherein the statin is selected from atorvastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, and simvastatin.

8. The method of claim 1 , wherein the compound of formula (I) is administered to the mammal together with the HMGCoA reductase inhibitor.

9. A method of reducing toxicity induced by a HMGCoA reductase inhibitor in a mammal, which method comprises administering to the mammal a therapeutically effective amount of a compound of formula (I):

and salt complexes thereof, wherein R is selected from the group consisting of amino, alkylamino, substituted alkylamino, dialkylamino, substituted dialkylamino, alkyloxy, substituted alkyloxy, aryloxy, substituted aryloxy, hydroxylamino, substituted hydroxylamino, O-alkyloxyamino, substituted O-alkyloxyamino, aminooxy, substituted aminoxy, N-alkylaminooxy, substituted N-alkylaminoxy, hydrazino, substituted hydrazino, alkylhydrazino, and substituted alkylhydrazino, and then administering to the mammal the HMGCoA reductase inhibitor in an amount that produces toxicity in the mammal in the absence of the administration of the compound of formula (I), whereby toxicity that would have been induced by the HMGCoA reductase inhibitor is reduced in the mammal by the administration of the compound of formula (I).

10. The method of claim 1 , wherein the compound of formula (I) is administered to the mammal following manifestation of toxicity by the mammal.

11. The method of claim 1 , wherein the mammal is a human.

12. A pharmaceutical composition comprising
(a) a HMGCoA reductase inhibitor,
(b) a compound of formula (I):

 and salt complexes thereof, wherein R is selected from the group consisting of amino, alkylamino, substituted alkylamino, dialkylamino, substituted dialkylamino, alkyloxy, substituted alkyloxy, aryloxy, substituted aryloxy, hydroxylamino, substituted hydroxylamino, O-alkyloxyamino, substituted O-alkyloxyamino, aminooxy, substituted aminoxy, N-alkylaminooxy, substituted N-alkylaminoxy, hydrazino, substituted hydrazino, alkylhydrazino, and substituted alkylhydrazino, and
(c) a pharmaceutically acceptable carrier.

13. A method of reducing toxicity induced by a HMGCoA reductase inhibitor in a mammal, which method comprises administering to the mammal a therapeutically effective amount of a compound of formula (I):

and salt complexes thereof, wherein R is selected from the group consisting of amino, alkylamino, substituted alkylamino, dialkylamino, substituted dialkylamino, alkyloxy, substituted alkyloxy, aryloxy, substituted aryloxy, hydroxylamino, substituted hydroxylamino, O-alkyloxyamino, substituted O-alkyloxyamino, aminooxy, substituted aminoxy, N-alkylaminooxy, substituted N-alkylaminoxy, hydrazino, substituted hydrazino, alkylhydrazino, and substituted alkylhydrazino, whereby toxicity induced by the HMGCoA inhibitor is reduced in the mammal,
wherein the compound of formula (I) is administered to the mammal following manifestation of toxicity by the mammal.

14. The method of claim 13 , wherein the alkyloxy or substituted alkyloxy is selected from —OMe, —OEt, and —OCH 2 CH 2 OH.

15. The method of claim 13 , wherein the aryloxy is —OPh.

16. The method of claim 13 , wherein the alkylamino or substituted alkylamino is selected from —NHMe, —NHEt, —NHCH 2 CH 2 OH, —NHCH 2 CH═CH 2 , —NHCH(CH 3 ) 2 , —NHCH 2 CH 2 NH 2 , and —NHcyclopropyl.

17. The method of claim 13 , wherein the dialkylamino is —N(CH 3 ) 2 or N-substituted pyrrolidinyl.

18. The method of claim 13 , wherein the HMGCoA reductase inhibitor is a statin.

19. The method of claim 18 , wherein the statin is selected from atorvastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, and simvastatin.

20. The method of claim 13 , wherein the method comprises administering the HMGCoA reductase inhibitor in a concentration that typically produces toxicity in the mammal and the compound of formula (I) is administered under conditions such that the toxicity is prevented.

21. The method of claim 13 , wherein the mammal is a human.

Assignees

• Univ Cornell

Inventors

• Sauve Anthony A
• Redanz Tianle Yang

Classifications

• C07H1/00

  Processes for the preparation of sugar derivatives · CPC title

• A61K31/706 Primary

  containing six-membered rings with nitrogen as a ring hetero atom · CPC title

• C07H19/048 Primary

  Pyridine radicals · CPC title

• A61K31/351

  not condensed with another ring · CPC title

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title