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| Product | Description | |
|---|---|---|
| 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 |
| 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 4-hydrate | Beta-nicotinamide adenine dinucleotide 4-hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BETA-NICOTINAMIDE ADENINE DINUCLEOTIDE TETRAHYDRATE, CRYSTALLINE, 98+%;Diphosphopyridine dinucleotide;beta-Nicotinamideadeninedinucleotidetetrahydratecrystalline;Beta-nicotinamide adenine dinucleotide tetrahydrate, 98+%, crystalline. Product Category: Heterocyclic Organic Compound. CAS No. 282730-13-6. Molecular formula: C21H35N7O18P2. Mole weight: 735.487. Product ID: ACM282730136. Alfa Chemistry ISO 9001:2015 Certified. | |
| beta-Nicotinamide adenine dinucleotide phosphate | NADP zwitterion is a NADP. It has a role as a fundamental metabolite. It is a conjugate base of a NADP(+). A coenzyme composed of ribosylnicotinamide 5'-phosphate (NMN) coupled by pyrophosphate linkage to the 5'-phosphate adenosine 2',5'-bisphosphate. It serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH). Synonyms: beta-NADP; NADP; TPN; Triphosphopyridine nucleotide; coenzyme II; Codehydrogenase II; Nadide phosphate; [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl][(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate. Grades: ≥ 90%. CAS No. 53-59-8. Molecular formula: C21H28N7O17P3. Mole weight: 743.41. |  |
| 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. | |
| 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 |
| β-Nicotinamide-Adenine Dinucleotide, Reduced Form (β-NADH) | NADH is a coenzyme that functions as a regenerating electron donor in catabolic processes including glycolysis, beta-oxidation and the citric acid cycle (Krebs cycle, TCA cycle). It participates in cell signaling events as well, for example as a substrate for the poly (ADP-ribose) polymerases (PARPs) during the DNA damage response. The NAD+/NADH dependent sirtuins play key roles in stress responses during events involving energy metabolism, with implications in cancer biology, diabetes and neurodegenerative disease. Group: Coenzymes. Synonyms. Enzyme Commission Number: EC 1.1.1.1. CAS No. 606-68-8. Purity: Dertermined by decrease in absorbance at 340 nm on enzymatic oxidation with ADH* at pH 10.0 > 95% *ADH = Alcohol dehydrogenase (yeast) (EC 1.1.1.1.). β-NADH. Mole weight: 709.41. Storage: Keep tightly stoppered in the dark below 5°C. Moisture will reduce the purity. For prolonged storage, keep below-20°C. Unstable in acids, but relatively stable at pH 10-11. 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; β-NADH. Cat No: NATE-0786. |  |
| beta-Nicotinamide adenine dinucleotide sodium salt | 1g Pack Size. Group: Biochemicals. Formula: C21H26N7NaO14P2. CAS No. 20111-18-6. Prepack ID 39483402-1g. Molecular Weight 685.41. See USA prepack pricing. | |
| beta-Nicotinamide adenine dinucleotide sodium salt | 5g Pack Size. Group: Biochemicals. Formula: C21H26N7NaO14P2. CAS No. 20111-18-6. Prepack ID 39483402-5g. Molecular Weight 685.41. See USA prepack pricing. | |
| Beta-Nicotinamide Adenine Dinucleotide Sodium Salt | A metabolite of Nicotine,which is a potent parasympathomimetic stimulant. Synonyms: β-DPN, β-NAD, Coenzyme 1, Cozymase, DPN, Diphosphopyridine nucleotide, NAD, Nadide. Grades: > 95%. CAS No. 20111-18-6. Molecular formula: C21H26N7O14P2. Na. Mole weight: 662.43 22.99. | |
| NAD (beta-Nicotinamide adenine dinucleotide) | 1g Pack Size. Group: Biochemicals. Formula: C21H27N7O14P2. CAS No. 53-84-9. Prepack ID 27828376-1g. Molecular Weight 663.43. See USA prepack pricing. | |
| 2-Nicotinamide-2,3,5-tri-O-acetyl-b-D-riboside bromide | 2-Nicotinamide-2,3,5-tri-O-acetyl-b-D-riboside bromide, a highly intriguing and multifaceted biomedicine, unveils its remarkable therapeutic prowess in combating an array of afflictions. Serving as an invaluable forerunner to nicotinamide adenine dinucleotide (NAD+), a quintessential coenzyme orchestrating cellular energy metabolism, this exceptional compound exhibits vast potential in lending respite to maladies encompassing cancer, neurodegenerative disorders, and metabolic aberrations. Gifting unparalleled regulation of cellular processes and DNA reparation, its impact on the intricate machinery of life is undoubtedly profound. Synonyms: 3-carbamoyl-1-(tri-O-acetyl-α-D-ribofuranosyl)-pyridinium,bromide; NICOTINAMIDE-BETA-D-RIBOSIDE-2,3,5-TRIACETATE BROMIDE. CAS No. 78687-38-4. Molecular formula: C17H21BrN2O8. Mole weight: 461.26. | |
| 2-Nicotinamide-b-D-riboside bromide | 2-Nicotinamide-b-D-riboside bromide, a versatile biomedicine, exhibits immense therapeutic potential in combatting diverse pathological conditions. It serves as a remarkable precursor to the indispensable cofactor nicotinamide adenine dinucleotide (NAD+), facilitating vital metabolic processes. Its efficacy has been extensively investigated, unveiling promising prospects for mitigating age-related afflictions, metabolic anomalies, and neurodegenerative maladies. Astounding in its versatility, 2-Nicotinamide-b-D-riboside bromide stands as a potent solution in the dynamic realm of biomedical interventions. Synonyms: 3-(Aminocarbonyl)-1-b-D-ribofuranosyl-pyridinium bromide; N1-(β-D-Ribofuranosyl)-3-aminocarbonylpyridinium bromide; NICOTINAMIDE-BETA-D-RIBOSIDE BROMIDE; 3-Carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide; 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyridin-1-ium-3-carboxamide bromide. CAS No. 78687-39-5. Molecular formula: C11H15BrN2O5. Mole weight: 335.15. | |
| 3-hydroxybutyryl-CoA dehydrogenase | This enzyme belongs to the family of oxidoreductases, to be specific those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (S)-3-hydroxybutanoyl-CoA:NADP+ oxidoreductase. Other names in common use include beta-hydroxybutyryl coenzyme A dehydrogenase, L(+)-3-hydroxybutyryl-CoA dehydrogenase, BHBD, dehydrogenase, L-3-hydroxybutyryl coenzyme A (nicotinamide adenine, dinucleotide phosphate), L-(+)-3-hydroxybutyryl-CoA dehydrogenase, and beta-hydroxybutyryl-CoA dehydrogenase. This enzyme participates in benzoate degradation via coa ligation and butanoate metabolism. Group: Enzymes. Synonyms: β-hydroxybutyryl coenzyme A dehydrogenase; L(+)-3-hydroxybutyryl-CoA dehydrogenase; BHBD; dehydrogenase, L-3-hydroxybutyryl coenzyme A (nicotinamide ade. Enzyme Commission Number: EC 1.1.1.157. CAS No. 39319-78-3. 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-0061; 3-hydroxybutyryl-CoA dehydrogenase; EC 1.1.1.157; 39319-78-3; β-hydroxybutyryl coenzyme A dehydrogenase; L(+)-3-hydroxybutyryl-CoA dehydrogenase; BHBD; dehydrogenase, L-3-hydroxybutyryl coenzyme A (nicotinamide adenine dinucleotide phosphate); L-(+)-3-hydroxybutyryl-CoA dehydrogenase; β-hydroxybutyryl-CoA dehydrogenase. Cat No: EXWM-0061. | |
| 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-NAD, Oxidized (Beta-NAD, Coenzyme I) | β-NAD, Oxidized (Beta-NAD, Coenzyme I). Group: Biochemicals. Alternative Names: Adenosine 5-(Trihydrogen Diphosphate), P?5-Ester with 3-(Aminocarbonyl)-1- β -D-ribofuranosyl pyridinium Hydroxide, Inner Salt; Pyridinium, 3-Carbamoyl-1- β-D-ribofuranosyl-, Hydroxide, 5?5-Ester with Adenosine 5-(Trihydrogen Pyrophosphate), Inner Salt (8CI); Adenine-nicotinamide Dinucleotide; CO-I; Codehydrase I; Codehydrogenase I; Coenzyme I; Cozymase I; DPN; Diphosphopyridine Nucleotide; Enzopride; NAD; NAD+; NSC 20272; Nadide; Nicotinamide-adenine Dinucleotide; Oxidized Diphosphopyridine Nucleotide; β-Diphosphopyridine Nucleotide; β-NAD; β-NAD+; β-Nicotinamide Adenine Dinucleotide; β-Nicotinamide Adenine Dinucleotide Hydrate. Grades: Highly Purified. CAS No. 53-84-9. Pack Sizes: 5g. 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. Grades: ≥ 90%. CAS No. 68141-45-7. Molecular formula: C21H27KN7O17P3. Mole weight: 781.50. | |
| glutamate synthase (NADPH) | Binds FMN, FAD, 2 [4Fe-4S] clusters and 1 [3Fe-4S] cluster. The reaction takes place in the opposite direction to that shown. The protein is composed of two subunits, α and &beta. The α subunit is composed of two domains, one hydrolysing L-glutamine to NH3 and L-glutamate (cf. EC 3.5.1.2, glutaminase), the other combining the produced NH3 with 2-oxoglutarate to produce a second molecule of L-glutamate (cf. EC 1.4.1.4, glutamate dehydrogenase [NADP+]). The β subunit transfers electrons to the cosubstrate. The NH3 is channeled through a 31 ? channel in the active protein. In the absence of the β subunit, coupling between the two domains of the α subunit...mmission Number: EC 1.4.1.13. CAS No. 37213-53-9. 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-1446; glutamate synthase (NADPH); EC 1.4.1.13; 37213-53-9; glutamate (reduced nicotinamide adenine dinucleotide phosphate) synthase; L-glutamate synthase; L-glutamate synthetase; glutamate synthetase (NADP); NADPH-dependent glutamate synthase; glutamine-ketoglutaric aminotransferase; NADPH-glutamate synthase; NADPH-linked glutamate synthase; glutamine amide-2-oxoglutarate aminotransferase (oxidoreductase, NADP); L-glutamine:2-oxoglutarate aminotransferase, NADPH oxidizing; GOGAT. Cat No: EXWM-1446. | |
| Isocitrate dehydrogenase (NAD+) from Bacteria, Recombinant | 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 o...namide adenine dinucleotide Isocitrate dehydrogenase; EC 1.1.1.41. Enzyme Commission Number: EC 1.1.1.41. CAS No. 9001-58-5. IDH. Mole weight: 40 kD (SDS-PAGE). Activity: > 40 Units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. Beta-ketoglutaric-isocitric carboxylase; IDH; Isocitrate dehydrogenase (NAD); Isocitric acid dehydrogenase; Isocitric dehydrogenase; NAD dependent Isocitrate dehydrogenase; NAD Isocitrate dehydrogenase; NAD isocitric dehydrogenase; NAD-linked Isocitrate dehydrogenase; NAD-specific Isocitrate dehydrogenase; Nicotinamide adenine dinucleotide Isocitrate dehydrogenase; EC 1.1.1.41. Cat No: NATE-1041. | |
| Isocitrate Dehydrogenase (NADP+) from Bacteria, Recombinant | Isocitrate dehydrogenase (IDH) (EC 1.1.1.42) 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 cof...rogenase (NADP+); EC 1.1.1.42; IDH; Isocitrate Dehydrogenase; Dual-cofactor-specific Isocitrate dehydrogenase; IDP; Isocitrate (NADP) dehydrogenase; Isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase; Isocitrate dehydrogenase (NADP); Isocitrate dehydrogenase (NADP-dependent); NADP isocitric dehydrogenase; NADP (+)-ICDH; NADP (+)-IDH; NADP (+)-linked Isocitrate dehydrogenase; NADP-dependent Isocitrate dehydrogenase; NADP-dependent isocitric dehydrogenase; NADP-linked Isocitrate dehydrogenase; NADP-specific Isocitrate dehydrogenase; Oxalosuccinate decarboxylase; Oxalsuccinic decarboxylase; Triphosphopyridine nucleotide-linked Isocitrate dehydrog | |
| Isocitrate Dehydrogenase (NADP+) from Yeast, Recombinant | Isocitrate dehydrogenase (IDH) (EC 1.1.1.42) 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: Isocitrate Dehydrogenase (NADP+); EC 1.1.1.42; IDH; Isocitrate . Enzyme Commission Number: EC 1.1.1.42. CAS No. 9028-48-2. IDH. Activity: r-ICDH activity = 100%. Storage: -20°C. Form: Liquid. Source: Pichia pastoris. Species: Yeast. Isocitrate Dehydrogenase (NADP+); EC 1.1.1.42; IDH; Isocitrate Dehydrogenase; Dual-cofactor-specific Isocitrate dehydrogenase; IDP; Isocitrate (NADP) dehydrogenase; Isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase; Isocitrate dehydrogenase (NADP); Isocitrate dehydrogenase (NADP-dependent); NADP | |
| 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 |
| NAD+, Lithium salt | NAD+, Lithium salt is the salt form of NAD+, which is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It plays a role in the activity of several enzymes, such as poly(ADP)-ribose polymerases and cADP-ribose synthases. NAD+ is commonly used as an oxidizing agent. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: β-Nicotinamide adenine Dinucleotide, Li; Beta-NAD lithium salt; Nicotinamide adenine dinucleotide lithium salt. CAS No. 64417-72-7. Molecular formula: C21H26LiN7O14P2. Mole weight: 669.362. | |
| NADP monosodium salt | Sodium salt hydrate form of NADP which is a coenzyme widely exist in living organism and commonly related to oxidation-reduction reactions. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: CO II, NA;COENZYME II SODIUM SALT;BETA-NADP MONOSODIUM SALT;BETA-NADP-NA;BETA-NADP SODIUM SALT;BETA-NADP SODIUM SALT, HYDRATE;BETA-NICOTINAMIDE-ADENINE DINUCLEOTIDE PHOSPHATE, MONOSODIUM SALT;BETA-NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE SODIUM SALT. Grades: >90.0%(LC). CAS No. 1184-16-3. Molecular formula: C21H28N7O17P3.Na. Mole weight: 766.40. | |
| 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 | |
| Nicotinamide-beta-D-riboside H-L-tartrate | Nicotinamide-beta-D-riboside H-L-tartrate is a cutting-edge compound, finding remarkable applicability in the comprehensive research of diverse pathological states, comprising metabolic abnormalities, neuropathologies and mitochondrial impairments. It diligently assumes the role of a bioavailable precursor, effectively replenishing nicotinamide adenine dinucleotide (NAD+), an indispensably pivotal coenzyme instrumental in governing cellular energetics and orchestrating seamless DNA mending. Synonyms: 3-Carbamoyl-1-(beta-D-ribofuranosyl)-pyridinium 2,3-dihydroybutanedioate(2S)(1:1). Molecular formula: C15H20N2O11. Mole weight: 404.33. | |
| NR-CL | Nicotinamide riboside is a precursor of nicotinamide adenine dinucleotide (NAD) and represents a source of vitamin B3. Synonyms: Nicotinamideribosidechloride; NicotinamideB-DRibosideChloride(WX900111); NicotinamideRiboside.Cl; Nicotimideribosidechloride; Pyridinium, 3-(aminocarbonyl)-1-β -D-ribofuranosyl-, chloride(1:1); 3-carbamoyChemicalbookl-1-((2R, 3R, 4S, 5R)-3, 4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-iumchloride; 3-Carbamoyl-1-(β -D-ribofuranosyl)pyridiniumchloride; 3-Carbamoyl-1-beta-D-ribofuranosylpyridiniumchloride. CAS No. 23111-00-4. Product ID: PAP-0088. Molecular formula: C11H15ClN2O5. Product Keywords: Other Active Pharmaceutical Ingredients; NR-CL; PAP-0088; ; C11H15ClN2O5; 23111-00-4. Appearance: White Powder. Chemical Name: Pyridinium,3-(aminocarbonyl)-1-β-D-ribofuranosyl-,chloride(1:1). Grade: Pharmaceutical Grade. Color: White. Solubility: Soluble to 100 mM in DMSO and to 100 mM in water. Storage: under inert gas (nitrogen or Argon) at 2-8°C. Product Description: Nicotinamide riboside is a precursor of nicotinamide adenine dinucleotide (NAD) and represents a source of vitamin B3. |  |
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