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| Product | Description | |
|---|---|---|
| Thionicotinamide adenine dinucleotide | Thionicotinamide adenine dinucleotide (Thio-NAD) is a dinucleotide substrate [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Thio-NAD. CAS No. 4090-29-3. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-131924. |  |
| Thionicotinamide Adenine Dinucleotide | Thionicotinamide Adenine Dinucleotide is utilized as a cofactor. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Thionicotinamide-DPN. CAS No. 4090-29-3. Molecular formula: C21H27N7O13P2S. Mole weight: 679.491. |  |
| NAD+ diphosphatase | This enzyme, described from plants, animals, and bacteria, can act on both reduced and oxidized forms of its substrate, although enzymes from different organisms have different preferences. Also acts on other dinucleotides, including NADP(H), FAD(H2), and the thionicotinamide analogues of NAD+ and NADP+. Group: Enzymes. Synonyms: NPY1 (gene name); nudC (gene name); NUDT7 (gene name); nicotinamide adenine dinucleotide pyrophosphatase; NADP pyrophosphatase; NADH pyrophosphatase; NAD+ phosphohydrolase. Enzyme Commission Number: EC 3.6.1.22. CAS No. 37289-33-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4606; NAD+ diphosphatase; EC 3.6.1.22; 37289-33-1; NPY1 (gene name); nudC (gene name); NUDT7 (gene name); nicotinamide adenine dinucleotide pyrophosphatase; NADP pyrophosphatase; NADH pyrophosphatase; NAD+ phosphohydrolase. Cat No: EXWM-4606. |  |
| NADH Thio, Reduced (Nicotinamide Adenine Dinucleotide), Thio-NADH) | Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transp...oth of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. For NAD, the reaction is thus:NAD+ + 2H -> NADH + H+. Group: Biochemicals. Alternative Names: Nicotinamide Adenine Dinucleotide; Thio-NADH; Thionicotinamide adenine dinucleotide. Grades: Highly Purified. CAS No. 1921-48-8. Pack Sizes: 100mg. Molecular Formula: C21H29N7O13SP2, Molecular Weight: 681.51. US Biological Life Sciences. |  Worldwide |
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