CAS 606-68-8
:Dinatrium-NADH
Beschreibung:
Dinatrium-NADH, auch bekannt als Disodium-Nicotinamid-Adenin-Dinukleotid, ist ein Coenzym, das eine entscheidende Rolle in verschiedenen biologischen Prozessen spielt, insbesondere in der Zellatmung und im Stoffwechsel. Es ist die reduzierte Form von NAD+ (Nicotinamid-Adenin-Dinukleotid) und ist an Redoxreaktionen beteiligt, indem es als Elektronentransporter fungiert. Die Disodiumsalzform verbessert seine Löslichkeit in wässrigen Lösungen und macht es bioverfügbarer für biochemische Anwendungen. Dinatrium-NADH ist typischerweise ein weißes bis off-white kristallines Pulver und ist hygroskopisch, was bedeutet, dass es Feuchtigkeit aus der Luft aufnehmen kann. Es ist unter normalen Bedingungen stabil, sollte jedoch vor Licht und extremen Temperaturen geschützt werden, um seine Wirksamkeit zu erhalten. In Laborumgebungen wird es häufig in enzymatischen Tests und Studien zum Energiestoffwechsel sowie in der Formulierung von Nahrungsergänzungsmitteln verwendet, die darauf abzielen, die Energieniveaus zu erhöhen und die Zellgesundheit zu unterstützen. Seine Rolle in der Elektronentransportkette unterstreicht seine Bedeutung für die ATP-Produktion und die allgemeine Zellfunktion.
Formel:C21H27N7Na2O14P2
InChl: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
InChI Key: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]
Synonyme:- 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
- Weitere Synonyme anzeigen
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18 Produkte.
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>Formel:C21H27N7Na2O14P2Reinheit:97%Farbe und Form:Powder, White to yellowMolekulargewicht:709.41Nicotinamide adenine dinucleotide (reduced form) disodium salt nutraceutical grade
CAS:Nicotinamide adenine dinucleotide (reduced form) disodium salt nutraceutical gradeReinheit:98%Farbe und Form:Beige PowderMolekulargewicht:709.40g/molβ-Nicotinamide adenine dinucleotide reduced form, disodium salt
CAS:Formel:C21H27N7Na2O14P2Reinheit:≥ 95.0%Farbe und Form:White to light-yellow crystalline powderMolekulargewicht:709.40 (anhydrous)Nicotinamide adenine dinucleotide (reduced form) disodium salt
CAS:Nicotinamide adenine dinucleotide (reduced form) disodium saltFormel:C21H27N7O14P2·2NaReinheit:>98%Farbe und Form:Beige PowderMolekulargewicht:709.40464g/molβ-Nicotinamide Adenine Dinucleotide Disodium Salt, reduced form [for Biochemical Research]
CAS:Formel:C21H27N7Na2O14P2Farbe und Form:White to Orange to Green powder to crystalMolekulargewicht: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>Formel:C21H27N7Na2O14P2Reinheit:98.05% - 99.85%Farbe und Form:Odorless Yellowish PowderMolekulargewicht:709.4b-NADH-d4 (d4 major) Diammonium Salt
CAS:Kontrolliertes ProduktFormel:C21H24D4N7O14P2NH3Farbe und Form:White To Off-WhiteMolekulargewicht: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>Formel:C21H27N7O14P2·2NaFarbe und Form:NeatMolekulargewicht: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>Formel:C21H27N7O14P2·2NaReinheit:Min. 98 Area-%Farbe und Form:White PowderMolekulargewicht: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>Formel:C21H29N7O14P2•Na2Reinheit:Min. 95%Molekulargewicht:711.42 g/molß-Nicotinamide Adenine Dinucleotide Disodium Salt(Reduced) (ß-NADH.Na2,DPNH.Na2) for cellculture,98%
CAS:Formel:C21H27N7O14P2Na2Reinheit:min. 98%Farbe und Form:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowMolekulargewicht:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) for MB, 98%
CAS:Formel:C21H27N7O14P2Na2Reinheit:min. 98%Farbe und Form:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowMolekulargewicht:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) extrapure, 98%
CAS:Formel:C21H27N7O14P2Na2Reinheit:min. 98%Farbe und Form:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowMolekulargewicht:709.46ß-Nicotinamide Adenine Dinucleotide Disodium Salt (Reduced) (ß-NADH.Na2, DPNH.Na2) PrimeDx, 98%
CAS:Formel:C21H27N7O14P2Na2Reinheit:min.98%Farbe und Form:White to pale yellow, Crystalline powder, Clear, Colourless to pale yellowMolekulargewicht:709.46
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