Method of making nicotinamide ribofuranoside salts, nicotinamide ribofuranoside salts as such, and uses thereof
The present invention relates to a method of making nicotinamide ribofuranosie salts, in particular pharmaceutically acceptable nicotinamide ribofuranoside salts. The invention further relates to the nicotinamide ribofuranoside salts as such, in particular carboxylic acid salts in crystalline form, and their use in nutritional supplements and pharmaceutical compositions.
1. A crystalline form of nicotinamide-β-D-ribofuranoside hydrogen L-malate, wherein the crystalline form is characterized by a powder X-ray diffraction pattern having one or more peaks as provided in Table 2, ±0.2 degrees two theta.
2. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 19.8±0.2, 21.5±0.2, and 25.8±0.2 degrees two theta.
3. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 17.7±0.2, 27.3±0.2, and 28.6±0.2 degrees two theta.
4. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 17.7±0.2, 19.8±0.2, 21.5±0.2, 25.8±0.2, 27.3±0.2, and 28.6±0.2 degrees two theta.
5. A crystalline form of nicotinamide-β-D-ribofuranoside hydrogen D-malate, wherein the crystalline form is characterized by a powder X-ray diffraction pattern having one or more peaks as provided in Table 1, ±0.2 degrees two theta.
6. The crystalline form of claim 5 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 22.5±0.2, 24.1±0.2 and 26.0±0.2 degrees two theta.
7. The crystalline form of claim 5 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 16.6±0.2, 22.5±0.2 and 24.1±0.2 degrees two theta.
8. A crystalline form of nicotinamide-β-D-ribofuranoside hydrogen DL-malate, wherein the crystalline form is characterized by a powder X-ray diffraction pattern having one or more peaks as provided in Table 3, ±0.2 degrees two theta.
9. The crystalline form of claim 8 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 16.7±0.2, 24.2±0.2 and 26.0±0.2 degrees two theta.
10. The crystalline form of claim 8 , wherein the crystalline form is characterized by a powder X-ray diffraction pattern having the following peaks 12.7±0.2, 22.5±0.2 and 25.0±0.2 degrees two theta.
11. A nutritional supplement comprising a crystalline form of claim 1 .
12. A pharmaceutical composition comprising a crystalline form of claim 1 .
13. A nutritional supplement comprising a crystalline form of claim 5 .
14. A pharmaceutical composition comprising a crystalline form of claim 5 .
15. A nutritional supplement comprising a crystalline form of claim 8 .
16. A pharmaceutical composition comprising a crystalline form of claim 8 .