CAS 606-68-8
:Dissódio NADH
Descrição:
Dissódio NADH, também conhecido como disódio nicotinamida adenina dinucleótido, é uma coenzima que desempenha um papel crucial em vários processos biológicos, particularmente na respiração celular e no metabolismo. É a forma reduzida do NAD+ (nicotinamida adenina dinucleótido) e está envolvida em reações redox, atuando como transportador de elétrons. A forma de sal disódico melhora sua solubilidade em soluções aquosas, tornando-a mais biodisponível para aplicações bioquímicas. Dissódio NADH é tipicamente um pó cristalino branco a off-white, e é higroscópico, o que significa que pode absorver umidade do ar. É estável em condições normais, mas deve ser protegido da luz e de temperaturas extremas para manter sua eficácia. Em ambientes de laboratório, é frequentemente utilizado em ensaios enzimáticos e estudos relacionados ao metabolismo energético, bem como na formulação de suplementos dietéticos destinados a aumentar os níveis de energia e apoiar a saúde celular. Seu papel na cadeia de transporte de elétrons sublinha sua importância na produção de ATP e na função celular geral.
Fórmula:C21H27N7Na2O14P2
InChI:InChI=1/C21H27N7O14P2.2Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;;/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37);;/q;2*+1/p-1/t10-,11-,13-,14-,15-,16-,20-,21-;;/m1../s1
Chave InChI:InChIKey=BCRIEPRHSZGQQO-WUEGHLCSSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](COP(OP(OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)N5C=C(C(N)=O)CC=C5)(=O)O)(=O)O)[C@H]1O.[Na]
Sinónimos:- Adenosine 5'-(trihydrogen diphosphate), 5'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, disodium salt
- Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, disodium salt
- Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosylnicotinamide, sodium salt (1:2)
- Adenosine 5'-(trihydrogen pyrophosphate), 5'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosylnicotinamide, disodium salt
- Adenosine 5′-(trihydrogen diphosphate), P′→5′-ester with 1,4-dihydro-1-β-<span class="text-smallcaps">D</span>-ribofuranosyl-3-pyridinecarboxamide, disodium salt
- Adenosine 5′-(trihydrogen diphosphate), P′→5′-ester with 1,4-dihydro-1-β-<span class="text-smallcaps">D</span>-ribofuranosylnicotinamide, sodium salt (1:2)
- Adenosine 5′-(trihydrogen pyrophosphate), 5′→5′-ester with 1,4-dihydro-1-β-<span class="text-smallcaps">D</span>-ribofuranosylnicotinamide, disodium salt
- Dihidronicotinamida-Adenina-Dinucleotido, Sal Disodica
- Dihydronicotinamid-adenin-dinucleotid, Dinatriumsalz
- Dihydronicotinamide-adenine-dinucleotide, sel de disodium
- Disodium NADH
- NADH disodium salt
- Nadh
- Nicotinamide adenine dinucleotide, disodium salt
- Nicotinamide-adenine dinucleotide, reduced, disodium salt
- beta-Nicotinamide adenine dinucleotide disodium salt
- disodium [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl [[(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-oxido-phosphoryl] phosphate
- β-NADH
- β-Nicotinamide adenine dinucleotide disodium salt
- Nadide sodium
- DPNH DISODIUM SALT
- BIURET REAGENT WORKING SOLUTION
- DPNH
- Coenzyme I reduced disodium salt
- NADH,NADH DISODIUM SALT
- LB MODIFIED IN BOTTLES 1000ML
- Codehydrase I Reduced
- DIPHOSPHOPYRIDINE NUCLEOTIDE
- BETA-NADH DISODIUM
- NADH2
- DPNH, NA2
- B-NAD REDUCED FORM DISODIUM
- Codehydrogenase I Reduced
- BETA-NAD REDUCED FORM DISODIUM
- Co I reduced
- beta-Nicotinamide ad
- BETA-DPNH DISODIUM SALT
- DPNH2-NA2
- NADH 2Na
- CoenzyMe I Reduced
- NADH (sodium salt)
- Reduced Diphosphopyridine Nucleotide
- Reduced Codehydrogenase I
- BETA-NADH DISODIUM SALT
- β-NADH/β-DPNH
- Reduced NcotinaMide Adenine Diphosphate
- ENADA
- N A D H, REDUCED FORM, DISODIUM
- NADH disodiuM salt, trihydrate, reduced
- CozyMase I Reduced
- NADH-NA2
- N 8129
- Dihydrocodehydrogenase I
- B-NAD, REDUCED, DISODIUM
- BETA-NADH 2NA
- Diphosphopyridine nucleotide reduced
- Ver mais sinónimos
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18 produtos.
β-Nicotinamide adenine dinucleotide reduced disodium salt, 97%
CAS:<p>-Nicotinamide adenine dinucleotide (NAD+) and -Nicotinamide adenine dinucleotide, reduced (NADH) comprise a coenzyme redox pair (NAD+:NADH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. In addition to its redox function, NAD+/NADH is a donor of ADP-ribose units in ADP-r</p>Fórmula:C21H27N7Na2O14P2Pureza:97%Cor e Forma:Powder, White to yellowPeso molecular:709.41Nicotinamide adenine dinucleotide (reduced form) disodium salt nutraceutical grade
CAS:Nicotinamide adenine dinucleotide (reduced form) disodium salt nutraceutical gradePureza:98%Cor e Forma:Beige PowderPeso molecular:709.40g/molβ-Nicotinamide adenine dinucleotide reduced form, disodium salt
CAS:Fórmula:C21H27N7Na2O14P2Pureza:≥ 95.0%Cor e Forma:White to light-yellow crystalline powderPeso molecular:709.40 (anhydrous)Nicotinamide adenine dinucleotide (reduced form) disodium salt
CAS:Nicotinamide adenine dinucleotide (reduced form) disodium saltFórmula:C21H27N7O14P2·2NaPureza:>98%Cor e Forma:Beige PowderPeso molecular:709.40464g/molβ-Nicotinamide Adenine Dinucleotide Disodium Salt, reduced form [for Biochemical Research]
CAS:Fórmula:C21H27N7Na2O14P2Cor e Forma:White to Orange to Green powder to crystalPeso molecular:709.41NADH disodium salt
CAS:<p>NADH disodium salt hydrate, a reduced NAD form, donates electrons and gets oxidized to NAD+ in reduction reactions.</p>Fórmula:C21H27N7Na2O14P2Pureza:98.05% - 99.85%Cor e Forma:Odorless Yellowish PowderPeso molecular:709.4b-NADH-d4 (d4 major) Diammonium Salt
CAS:Produto ControladoFórmula:C21H24D4N7O14P2NH3Cor e Forma:White To Off-WhitePeso molecular:703.53b-NADH Disodium Salt
CAS:<p>Stability Hygroscopic<br>Applications One of the biologically active forms of nicotinic acid. Serves as a coenzyme of hydrogenases and dehydrogenases. NAD usually acts as a hydrogen acceptor, forming NADH which then serves as a hydrogen donor in the respiratory chain. Present in living cells primarily in the reduced form (NADPH) and is involved in synthetic reactions. Occurs in 2 forms, α-NAD and β-NAD, distinguished by the configuration of the ribosyl nicotinamide linkage. Only the β-anomer is bioactive.<br>References Bartlett, G.R., et al.: J. Biol. Chem., 234, 449 (1959), Dixon, M., et al.: Science, 132, 1548 (1960), Heyes, D., et al.: Biochemistry, 43, 8265 (2004), Dietzek, B., et al.: Chem. Phys. Chem., 7, 1727 (2006),<br></p>Fórmula:C21H27N7O14P2·2NaCor e Forma:NeatPeso molecular:709.40b-Nicotinamide adenine dinucleotide reduced form, disodium salt
CAS:<p>β-Nicotinamide adenine dinucleotide reduced form, most commonly known as NADH, is a cofactor involved in the electron transport chain, in the metabolism of amino acids and many other cellular processes such as the synthesis of ATP. It is also a substrate for glutathione peroxidase and superoxide dismutase. The reduced form of NADH can be used as an indicator for glutathione peroxidase activity. In addition, it has been shown to have antioxidant properties by reducing reactive oxygen species (ROS) and inhibiting lipid peroxidation. This product has been used in formulations of synthetic drugs for the treatment of women with long-term effects of menopause, such as osteoporosis and cardiovascular disease. It has also been used in the production of alginate gel, which can be used to create scaffolds for tissue engineering applications. More recently, in bioorganic chemistry, NADH has been used as a source of hydride species for reduction reactions.</p>Fórmula:C21H27N7O14P2·2NaPureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:709.4 g/molβ-Nicotinamide adenine dinucleotide, reduced form, disodium
CAS:<p>β-Nicotinamide adenine dinucleotide reduced form, most commonly known as NADH, is a cofactor involved in the electron transport chain, in the metabolism of amino acids and many other cellular processes such as the synthesis of ATP. It is also a substrate for glutathione peroxidase and superoxide dismutase. The reduced form of NADH can be used as an indicator for glutathione peroxidase activity. In addition, it has been shown to have antioxidant properties by reducing reactive oxygen species (ROS) and inhibiting lipid peroxidation. This product has been used in formulations of synthetic drugs for the treatment of women with long-term effects of menopause, such as osteoporosis and cardiovascular disease. It has also been used in the production of alginate gel, which can be used to create scaffolds for tissue engineering applications. Lately, in bioorganic chemistry, NADH has been used as a source of hydride species for reduction reactions.</p>Fórmula:C21H29N7O14P2•Na2Pureza:Min. 95%Peso molecular:711.42 g/molß-Nicotinamide Adenine Dinucleotide Disodium Salt(Reduced) (ß-NADH.Na2,DPNH.Na2) for cellculture,98%
CAS:Fórmula:C21H27N7O14P2Na2Pureza:min. 98%Cor e Forma:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowPeso molecular:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) for MB, 98%
CAS:Fórmula:C21H27N7O14P2Na2Pureza:min. 98%Cor e Forma:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowPeso molecular:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) extrapure, 98%
CAS:Fórmula:C21H27N7O14P2Na2Pureza:min. 98%Cor e Forma:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowPeso molecular:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) PrimeDx, 98%
CAS:Fórmula:C21H27N7O14P2Na2Pureza:min.98%Cor e Forma:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowPeso molecular:709.46
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