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| Product | Description | |
|---|---|---|
| Adenine phosphate salt | Adenine phosphate salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Adenine phosphate, 52175-10-7, 6-Aminopurine phosphate, 7H-Purin-6-amine phosphate, 1H-Purin-6-amine, phosphate, 70700-30-0, EINECS 257-702-7, PubChem9684, SureCN283728, SureCN283729, AC1L550T, MolPort-003-984-187, MolPort-006-108-180, phosphoric acid; 7H-purin-6-amine, 6-amino-1H-purine; phosphoric acid, AKOS015895413, AKOS015961504, AKOS016008799, AC-5490, AM83910. Product Category: Amines. Appearance: white crystalline powder. CAS No. 70700-30-0. Molecular formula: C4H12ClNO. Mole weight: 233.12. Purity: Purity >98%. IUPACName: phosphoric acid;7H-purin-6-amine. Canonical SMILES: C1=NC2=C(N1)C(=NC=N2)N.OP(=O)(O)O. ECNumber: 257-702-7. Product ID: ACM70700300. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Adenine phosphate salt 99+% (HPLC) | Adenine phosphate salt 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. |  Worldwide |
| 3-Acetylpyridine-adenine dinucleotide phosphate, reduced form, tetrasodium salt (APADPH) | Molecular Formula: C22H32N6O17P3. Group: Coenzymes. Synonyms: APADPH. Enzyme Commission Number: EC 1.1.1.1. Purity: > 92% when determined by enzymatic analysis with glutamate dehydrogenase at pH 7.5. APADPH. Mole weight: 745.45 (as anhydrous free acid) 886.41 (APADPH.Na4.3H2O). Storage: Keep tightly stoppered in the dark below 5°C. Moisture will accelerate the purity reduction. For prolonged storage keep below - 20°C. APADPH. Cat No: NATE-0080. |  |
| 3-Acetylpyridine adenine dinucleotide phosphate sodium salt | 3-Acetylpyridine adenine dinucleotide phosphate sodium salt is a highly potent and essential coenzyme employed extensively in diverse biomedical areas, exhibiting paramount significance in cellular energy metabolism. Furthermore, it finds common employment in investigating redox reactions and enzyme kinetics. Synonyms: Adenosine 5'-(trihydrogen diphosphate), 3'-(dihydrogen phosphate), P'→5'-ester with 3-acetyl-1-β-D-ribofuranosylpyridinium, inner salt, disodium salt. CAS No. 102029-67-4. Molecular formula: C22H29N6O17P3.2Na. Mole weight: 788.40. |  |
| Beta-nicotinamide adenine dinucleotide 3'-phosphate reduced from sodium salt | Beta-nicotinamide adenine dinucleotide 3'-phosphate reduced from sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: beta-Nicotinamide adenine dinucleotide 3'-phosphate reduced from sodium salt;beta-Nicotinamide adenine dinucleotide 3'-phosphate sodium salt hydrate. Product Category: Heterocyclic Organic Compound. CAS No. 50443-29-3. Molecular formula: C21H27N7O17P3?xNa+?yH2O. Mole weight: 765.39. Product ID: ACM50443293. Alfa Chemistry ISO 9001:2015 Certified. | |
| beta-Nicotinamide adenine dinucleotide phosphate disodium salt | 1g Pack Size. Group: Biochemicals. Formula: C21H26N7Na2O17P3. CAS No. 24292-60-2. Prepack ID 42474095-1g. Molecular Weight 787.37. See USA prepack pricing. |  |
| beta-Nicotinamide adenine dinucleotide phosphate monosodium salt (NADP sodium salt) | 1g Pack Size. Group: Biochemicals. Formula: C21H27N7O17P3 · Na. CAS No. 1184-16-3. Prepack ID 34796500-1g. Molecular Weight 765.39. See USA prepack pricing. | |
| β-Nicotinamide adenine dinucleotide phosphate, reduced tetra(cyclohexylammonium) salt | β-Nicotinamide adenine dinucleotide 2'-phosphate (NADP+) and β-Nicotinamide adenine dinucleotide 2'-phosphate, reduced (NADPH) comprise a coenzyme redox pair (NADP+:NADPH) that work together in a wide range of enzyme catalyzed oxidation reduction reactions. One of the pairs actions is that it facilitates electron transfer in anabolic reactions such as lipid and cholesterol biosynthesis and fatty acyl chain elongation. The NADP+/NADPH redox pair is also used in a variety of antioxidation mechanisms where it protects against reactive oxidation species accumulation. NADPH is generated in vivio by the pentose phosphate pathway (PPP). Applications: An electron donor and a cofactor for nitric oxide synthetase. Group: Coenzymes. Synonyms: β-NADPH; NADPH; TPNH. CAS No. 100929-71-3. Purity: ≥95%. Mole weight: 1142.12. Appearance: Powder. Form: Solid. β-NADPH; NADPH; TPNH; β-Nicotinamide adenine dinucleotide phosphate, reduced tetra(cyclohexylammonium) salt; 100929-71-3. Cat No: COEC-079. | |
| beta-Nicotinamide Adenine Dinucleotide Phosphate Tetrasodium Saltreduced form[for Biochemical Research] | beta-Nicotinamide Adenine Dinucleotide Phosphate Tetrasodium Saltreduced form[for Biochemical Research]. Group: Molecular Biology. Grades: Purified. CAS No. 2646-71-1. Pack Sizes: 100mg. Molecular Formula: C21H30N7O17P3. US Biological Life Sciences. | Worldwide |
| b-Nicotinamide adenine dinucleotide 3'-phosphate sodium salt hydrate | b-Nicotinamide adenine dinucleotide 3'-phosphate sodium salt hydrate, a pivotal coenzyme in the biomedical arena, exhibits its significance as a redox carrier and electron donor in diverse metabolic reactions. With its application in the amelioration of oxidative stress-induced ailments, including cardiovascular diseases and neurological disorders, this product assumes a critical function in cellular energy synthesis and the preservation of cellular well-being. Imbibed with indispensability, it perpetuates the vitality of the biotic system. Molecular formula: C21H27N7O17P3·xNa·yH20. Mole weight: 742.40 (anhydrous free acid). | |
| b-Nicotinamide adenine dinucleotide phosphate disodium salt | b-Nicotinamide adenine dinucleotide phosphate disodium salt, an indispensable coenzyme, demonstrates pivotal significance in diverse biochemical reactions. This coveted compound finds extensive employment within the biomedical domain, catering to research and therapeutic exigencies. Its multifarious application encompasses the meticulous scrutiny of cellular metabolism, DNA repair mechanisms and intricate redox reactions. Moreover, it assumes a vital role in alleviating maladies associated with oxidative stress, namely neurodegenerative disorders and cardiovascular ailments. Molecular formula: C21H26N7O19P3·2Na. Mole weight: 819.37. | |
| b-Nicotinamide adenine dinucleotide phosphate disodium salt | b-Nicotinamide adenine dinucleotide phosphate disodium salt. Group: Biochemicals. Alternative Names: b-NADH phosphate disodium salt. Grades: Highly Purified. CAS No. 24292-60-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C21H26N7Na2O17P3. US Biological Life Sciences. | Worldwide |
| b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate | b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate exemplifies an essential coenzyme that assumes a pivotal function in diverse biochemical reactions. This compound emerges as uniquely advantageous towards interrogating cellular metabolism, enzyme kinetics and redox reactions. Synonyms: coenzyme II; b-NADP-K; Triphosphopyridine nucleotide potassium salt; TPN; [5-(6-aminopurin-9-yl)-3-hydroxy-4-(oxyphosphinyloxyphosphinyl)oxolan-2-yl]met hyl{[5-(3-carbamoylpyridyl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxyphosphoryl)hydrogen phosphate,potassium salt; Beta-nadp potassium salt; Nadp monopotassium salt. Grade: ≥ 90%. CAS No. 68141-45-7. Molecular formula: C21H27KN7O17P3. Mole weight: 781.50. | |
| b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate | b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate. Group: Biochemicals. Alternative Names: coenzyme II; b-NADP-K; Triphosphopyridine nucleotide potassium salt; TPN. Grades: Highly Purified. CAS No. 68141-45-7. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C21H27KN7O17P3. US Biological Life Sciences. | Worldwide |
| b-Nicotinamide adenine dinucleotide phosphate, reduced form, disodium salt | b-Nicotinamide adenine dinucleotide phosphate, reduced form, disodium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| b-Nicotinamide Adenine Dinucleotide Phosphate, reduced form, tetrasodium salt ( β-NADPH) | One of the biologically active forms of nicotinic acid. Differs from NAD by an additional phosphate group at the 2-position of the adenosine moiety. Serves as a coenzyme of hydrogenases and dehydrogenases. Present in living cells primarily in the reduced form (NADPH) and is involved in synthetic reactions. Group: Biochemicals. Alternative Names: 2'-(Dihydrogen Phosphate) 5'-(Trihydrogen Pyrophosphate) adenosine 5'5'-Ester 1,4-Dihydro-1- β -D-ribofuranosyl nicotinamide Tetrasodium Salt Hydrate; β-NADPH; 2?-NADPH Hydrate; Coenzyme II Reduced Tetrasodium Salt Hydrate; Triphosphopyridine Nucleotide Reduced Tetrasodium Salt Hydrate; Dihydronicotinamide Adenine Dinucleotide Phosphate Tetrasodium Salt Hydrate. Grades: Highly Purified. CAS No. 2646-71-1. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: C??H??N?Na?O??P?; xH?O, Molecular Weight: 833.35. US Biological Life Sciences. | Worldwide |
| ?-Nicotinamide adenine dinucleotide 2?-phosphate reduced tetrasodium salt hydrate | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Nicotinic acid adenine dinucleotide phosphate sodium salt | ?92.5%. Group: Fluorescence/luminescence spectroscopy. | |
| 3-Acetylpyridine adenine dinucleotide phosphate | 3-Acetylpyridine adenine dinucleotide phosphate is a pivotal molecule, assuming an indispensable function in redox reactions. Served as a coenzyme within an array of metabolic pathways, particularly the electron transport chain, this compound assumes an imperious role in energy generation. Synonyms: Adenosine 5'-(trihydrogen diphosphate), 3'-(dihydrogen phosphate), P'→5'-ester with 3-acetyl-1-β-D-ribofuranosylpyridinium, inner salt. CAS No. 150729-98-9. Molecular formula: C22H29N6O17P3. Mole weight: 742.42. | |
| Adenosine 5'-diphosphate monopotassium salt | Adenosine 5'-diphosphate (ADP) is an adenine nucleotide containing two phosphate groups esterified to the sugar moiety at the 5' position. It is produced by dephosphorylation of adenosine 5'-triphosphate by ATPases and can be converted back to ATP by ATP synthases. Synonyms: Adenosine 5'-(trihydrogen diphosphate), monopotassium salt; Adenosine 5'-Diphosphate Potassium Salt; 5'-ADP monopotassium salt; ADP monopotassium salt. Grade: ≥95%. CAS No. 70285-70-0. Molecular formula: C10H14KN5O10P2. Mole weight: 465.29. | |
| Adenosine 5'-monophosphate disodium salt | Adenosine 5'-monophosphate disodium salt is a pivotal compound in the biomedical industry, exhibiting as an elemental constituent concerning cellular energy metabolism while simultaneously serving as a precursor facilitating adenosine triphosphate (ATP) research. Synonyms: 5'-Adenylic acid, sodium salt (1:2); 5'-Adenylic acid, disodium salt; 5'-AMP disodium salt; Adenosine 5'-phosphate disodium salt; Adenylic acid disodium salt; AMP disodium salt; Disodium 5'-AMP; Disodium 9-(β-D-ribofuranosyl)adenine 5'-monophosphate; Disodium adenosine 5'-phosphate; Disodium adenylate; Disodium AMP; Adenosine Phosphate Disodium; 5'-AMP disodium salt; Disodium adenosine 5'-phosphate. Grade: 98%. CAS No. 4578-31-8. Molecular formula: C10H12N5Na2O7P. Mole weight: 391.19. | |
| a-Nicotinamide mononucleotide | a-Nicotinamide mononucleotide is a pivotal intermediate in the bioresearch of nicotinamide adenine dinucleotide (NAD+), finding applications in studying the aging process and preserving neural integrity. Evidentially, it possesses the ability to stimulate sirtuin 1 is an NAD+-dependent enzyme, thereby augmenting mitochondrial functionality and fortifying cellular energy metabolism. Synonyms: 3-Carbamoyl-1-a-D-ribofuranosylpyridinium hydroxide,5'-phosphate, inner salt; α-nicotinamide mononucleotide; α-Nicotinamid-nucleotid; 3-carbamoyl-1-(O5-phosphono-α-D-ribofuranosyl)-pyridinium betaine; ((2R,3S,4R,5S)-5-(3-carbamoylpyridinium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate. CAS No. 7298-94-4. Molecular formula: C11H15N2O8P. Mole weight: 334.22. | |
| β-Nicotinic Acid Mononucleotide | A nucleotide of nicotinic acid which is produced from quinolinic acid by quinolinate phosphoribosyl transferase via transfer of a phosphoribose group. It is an intermediate of nicotinic acid adenine dinucleotide (NaAD) which is then converted to NAD via amidation and in turn converted to NADPH. Group: Biochemicals. Alternative Names: 3-Carboxy-1-(5-O-phosphono- β -D-ribofuranosyl) pyridinium Inner Salt; 3-Carboxy-1- β -D-ribofuranosyl pyridinium Hydroxide 5'-Phosphate Inner Salt; Nicotinate Mononucleotide; Nicotinate Ribonucleotide; Nicotinic Acid Ribonucleotide; Nicotinic Acid Ribotide; Nicotinic Mononucleotide; β-NaMN. Grades: Highly Purified. CAS No. 321-02-8. Pack Sizes: 1mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Leuconostoc mesenteroides Glucose-6-phosphate Dehydrogenase, Recombinant | Glucose-6-phosphate dehydrogenase (G6PD or G6PDH) (EC 1.1.1.49) is a cytosolic enzyme that catalyzes the chemical reaction:D-glucose 6-phosphate + NADP+ <-> 6-phospho-D-glucono-1,5-lactone + NADPH + H+. This enzyme is in the pentose phosphate pathway, a metabolic pathway that supplies reducing energy to cells (such as erythrocytes) by maintaining the level of the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH). Glucose 6-phosphate dehydrogenase (g-6-p-dh) is a key regulatory enzyme in the first step of the pentose phosphate pathway. g-6-p-dh is a glycoprotein with a molecular mass of 128 kda (gel filtration). Applications: Glucose-6-phosphate...its/mg protein (biuret). Storage: 2-8°C. Form: Type I, Lyophilized powder containing Ficoll and Tris buffer salts; Type II, ammonium sulfate suspension, Supplied in 3.2M ammonium sulfate containing 50mM Tris and 1mM magnesium chloride, pH 7.5. Source: E. coli. Species: Leuconostoc mesenteroides. EC 1.1.1.49; NADP-glucose-6-phosphate dehydrogenase; Zwischenferment; D-glucose 6-phosphate dehydrogenase; glucose 6-phosphate dehydrogenase (NADP); NADP-dependent glucose 6-phosphate dehydrogenase; 6-phosphoglucose dehydrogenase; Entner-Doudoroff enzyme; glucose-6-phosphate 1-dehydrogenase; G6PDH; GPD; glucose-6-phosphate dehydrogenase; 9001-40-5. Cat No: DIA-323. | |
| NADP monosodium salt | NADP, Monosodium Salt is a coenzyme that is widely distributed in living matter. Participates in oxidation-reduction reactions. Applications: A coenzyme that is widely distributed in living matter. Group: Coenzymes. Synonyms: Nicotinamide adenine dinucleotide phosphate monosodium salt; TPN. CAS No. 1184-16-3. Purity: >97%. Mole weight: 765.39. Form: Solid. Nicotinamide adenine dinucleotide phosphate monosodium salt; TPN; NADP monosodium salt; 1184-16-3. Cat No: COEC-001. | |
| Native Candida utilis L-Glutamic Dehydrogenase (NADP) | L-glutamic dehydrogenase catalyzes the conversion of glutamate to α-ketoglutarate. Group: Enzymes. Synonyms: L-Glutamic Dehydrogenase; EC 1.4.1.4; 9029-11-2; glutamic dehydrogenase; dehydrogenase, glutamate (nicotinamide adenine dinucleotide (phosphate)); glutamic acid dehydrogenase; L-glutamate dehydrogenase; L-glutamic acid dehydrogenase; NAD (P)-glutamate dehydrogenase; NAD (P)H-dependent glutamate dehydrogenase; glutamate dehydrogenase (NADP). Enzyme Commission Number: EC 1.4.1.4. CAS No. 9029-11-2. GLDH. Activity: 50-200 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing potassium phosphate buffer salt. Source: Candida utilis. L-Glutamic Dehydrogenase; EC 1.4.1.4; 9029-11-2; glutamic dehydrogenase; dehydrogenase, glutamate (nicotinamide adenine dinucleotide (phosphate)); glutamic acid dehydrogenase; L-glutamate dehydrogenase; L-glutamic acid dehydrogenase; NAD (P)-glutamate dehydrogenase; NAD (P)H-dependent glutamate dehydrogenase; glutamate dehydrogenase (NADP). Cat No: NATE-0394. | |
| Native Porcine Isocitric Dehydrogenase (NADP) | Isocitrate dehydrogenase (IDH) is an enzyme that catalyzes the oxidative decarboxylation of Isocitrate, producing alpha-ketoglutarate (α-ketoglutarate) and CO2. This is a two-step process, which involves oxidation of Isocitrate (a secondary alcohol) to oxalosuccinate (a ketone), followed by the decarboxylation of the carboxyl group beta to the ketone, forming alpha-ketoglutarate. In humans, IDH exists in three isoforms:IDH3 catalyzes the third step of the citric acid cycle while converting NAD+ to NADH in the mitochondria. The isoforms IDH1 and IDH2 catalyze the same reaction outside the context of the citric acid cycle and use NADP+ as a cofactor instead of NAD+. They localize to the cytosol as well as the mitochondrion and peroxisome. Group: Enzymes. Synonyms: oxalosuccinate decarboxylase; Isocitrate dehyd. Enzyme Commission Number: EC 1.1.1.42. CAS No. 9028-48-2. IDH. Activity: Type I, 0.5-3.0 unit/mg solid; Type II, 3-20 units/mg protein. Storage: -20°C. Form: Type II, buffered aqueous glycerol solution, Solution in 50% glycerol in EDTA buffer salts, pH 6.0. Source: Porcine heart. Species: Porcine. oxalosuccinate decarboxylase; Isocitrate dehydrogenase (NADP); oxalsuccinic decarboxylase; Isocitrate (NADP) dehydrogenase; Isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase; NADP-specific Isocitrate dehydrog | |
| Native Yeast Alcohol dehydrogenase | Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH). In Humans and many other animals, they serve to break down alcohols that otherwise are toxic, and they also participate in geneRation of useful aldehyde, ketone, or alcohol groups during biosynthesis of various metabolites. In yeast, plants, and many bacteria, some alcohol dehydrogenases catalyze the opposite reaction as part of fermentation to ensure a constant supply of NAD+. Dehydrogenase that catalyzes the interconversion of alcoho...rimary alcohol dehydrogenase; yeast alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.1.1. CAS No. 9031-72-5. Activity: >300 U/mg. Appearance: White lyophilizate (50 mg lyophilizate contain approximately 30 mg enzyme protein,15 mg sucrose, 5 mg phosphate). Storage: -20°C. Form: Solids containing <2% Citrate buffer salts. Source: Yeast. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Cat No: NATE-0975. | |
| 2-Chloroadenosine 5'-Monophosphate Ditriethylamine Salt | A metabolite of 2-Chloroadenosine; an adenine nucleotide receptor. Synonyms: 2-Chloro-5'-adenylic Acid; 2-Chloro-adenosine 5'-(Dihydrogen Phosphate) Ditriethylamine; 2-Chloro-AMP Ditriethylamine. Grade: 96%. CAS No. 52621-99-5. Molecular formula: C22H43ClN7O7P. Mole weight: 584.05. | |
| β-NADH, Reduced Disodium Salt (Nicotinamide Adenine Dinucleotide) | 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 tran...accomplished by the removal of hydrogen atoms. Both 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. Group: Biochemicals. Alternative Names: β-DPNH; β-NADH; DPNH; Diphosphopyridine nucleotide, reduced form; NADH. Grades: Highly Purified. CAS No. 606-68-8. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C21H27N7O14P2Na2, Molecular Weight: 709.41. US Biological Life Sciences. | Worldwide |
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