Dihydronicotinamid-adenin-dinucleotid, Dinatriumsalz
beta-Nicotinamide adenine dinucleotide, reduced disodium salt hydrate
Grundinformationen
- CAS
606-68-8- Standard-SMILES
N=C([O-])C1=CN([C@@H]2O[C@H](COP(=O)([O-])OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1.[Na+].[Na+]- InChIKey
QRGNQKGQENGQSE-WUEGHLCSSA-L- Summenformel
- C21H27N7Na2O14P2
- Durchschnittliche Molmasse
- 709,4 g/mol
- Monoisotopische Masse
- 709,08866112
Überblick
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Namen und Bezeichner
- Bevorzugter Name
- beta-Nicotinamide adenine dinucleotide, reduced disodium salt hydrate
- IUPAC
- disodium;1-[(2R,3R,4S,5R)-5-[[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-oxidophosphoryl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]-4H-pyridine-3-carboximidate
- Lokaler Name
- Dihydronicotinamid-adenin-dinucleotid, Dinatriumsalz
- Englischer Name
- NADH, disodium salt
- Summenformel
- C21H27N7Na2O14P2
- Molmasse
- 709.4
Namen und Synonyme
606-68-8beta-Nicotinamide adenine dinucleotide, reduced disodium salt hydrateMFCD00036200C21H27N7Na2O14P2disodium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-oxido-phosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoyl-4H-pyridin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl phosphateΒ-NADHNADH DISODIUM SALTNADH-NA2DIPHOSPHOPYRIDINE NUCLEOTIDEBETA-NICOTINAMIDE ADENINE DINUCLEOTIDE REDUCED DISODIUM SALTNADH 2NaBETA-NADH 2NA
Weitere Namen anzeigen
NADH (sodium salt)β-NADH Disodium Saltbeta-NICOTINAMIDE ADENINE DINUCLEOTIDE REDUCED
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 324 Ų
- H-Brücken-Donoren
- 7
- H-Brücken-Akzeptoren
- 20
- Frei drehbare Bindungen
- 11
- Schwere Atome
- 46
- Formalladung
- 0
- Komplexität
- 1.220
Physikochemische Eigenschaften
- Schmelzpunkt
- 140 · 140-142°C
- Dichte
- 1.955 at · 1.955 at 20℃
- Dampfdruck
- 0.73 Pa · 0.73Pa at 20-50℃
- storage temp.
- -20 °C · Inert atmosphere,Store in freezer, under -20°C
- Löslichkeit
- 2 O: · H2O: 50 mg/mL, clear to nearly clear, yellow
- Aggregatzustand
- Powder
- Farbe
- Yellow
- PH
- 7.5 · 7.5 (100mg/mL in water, ±0.5)
- Wasserlöslichkeit
- soluble
- BRN
- 5230241 · 5230241
- Stabilität
- Stable. Incompatible with strong oxidizing agents.
- Kosmetik-Inhaltsstoffe Funktionen
- SKIN CONDITIONINGSKIN CONDITIONING - EMOLLIENT
- InChIKey
- QRGNQKGQENGQSE-WUEGHLCSSA-L
- SMILES
- [Na+].[Na+].NC(=O)C1=CN(C=CC1)[C@H]2O[C@@H](COP([O-])(=O)OP([O-])(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@H](O)[C@@H]2O
- LogP
- -1.96 at · -1.96 at 21℃ and pH7
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Gefahrenhinweise
Regulatory InformationAdenosine 5'-(trihydrogen diphosphate), P'â5'-ester with 1,4-dihydro-1-.beta.-D-ribofuranosyl-3-pyridinecarboxamide, disodium salt: Does not have an individual approval but may be used under an appropriate group standard
Sicherheitsdaten
- F
- 3-10-23
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 29349990
- risk_code
- 23/24/25-36/37/38-39/23/24/25-40-22
- hazard_code
- Xn
- safety_code
- 26-36/37/39-45-24/25-36/37
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Anwendungen
Beschreibungβ-Nicotinamide adenine dinucleotide (NAD+) and β-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-ribosylaton (ADP-ribosyltransferases; poly(ADP-ribose) polymerases ) reactions and a precursor of cyclic ADP-ribose (ADP-ribosyl cyclases).
Ergänzende Hinweise
DefinitionNADH, disodium salt is a dehydrogenase complex that is the reduced formof NAD. As a reagent, NADH can be used in enzyme cycling assays to amplify detection of activity of biologically relevant enzymes or metabolites present in low concentrations.
DefinitionThe NAD+ Is the oxidized form, that is, a state in which it loses an electron. NADH is a reduced form of the molecule, which means that it gains the electron lost by NAD+. Redox reactions involving electron transfers play a central role in energy creation. When NAD+ takes an electron from glucose, it becomes NADH. NADH transports this electron to mitochondria where the cell can take the energy that is stored in the electron. NADH then donates the electron to oxygen, converting it back to NAD+.
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