Bio-Connect
Chemical Structure
Chemical Structure
Chemical Structure

beta-Nicotinamide adenine dinucleotide hydrate [53-84-9]

Research Use Only
CDX-N0222
Chemodex
CAS Number53-84-9
Product group Chemicals
Estimated Purity>98%
Molecular Weight663.43 (anhydrous basis)
Price on request
Packing Size
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    Chemodex
  • Product Name
    beta-Nicotinamide adenine dinucleotide hydrate [53-84-9]
  • Delivery Days Customer
    10
  • CAS Number
    53-84-9
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C21H27N7O14P2 . xH2O
  • Molecular Weight
    663.43 (anhydrous basis)
  • Scientific Description
    Chemical. CAS: 53-84-9. Formula: C21H27N7O14P2 . xH2O. MW: 663.43 (anhydrous basis). NAD+, known more formally as nicotinamide adenine dinucleotide, is a signaling molecule as well as a cofactor or substrate for many enzymes. It acts as an oxidizing agent, accepting electrons from other molecules while being converted to its reduced form, NADH. NAD+ is also essential for the activity of several enzymes, including poly(ADP)-ribose polymerases and cADP-ribose synthases. For example, it is used by some sirtuins to mediate protein deacetylation, producing O-acetyl-ADP-ribose and nicotinamide as well as the deacetylated protein. NAD+ is an important player and factor to research metabolic pathways and pathologies. - NAD+, known more formally as nicotinamide adenine dinucleotide, is a signaling molecule as well as a cofactor or substrate for many enzymes. It acts as an oxidizing agent, accepting electrons from other molecules while being converted to its reduced form, NADH. NAD+ is also essential for the activity of several enzymes, including poly(ADP)-ribose polymerases and cADP-ribose synthases. For example, it is used by some sirtuins to mediate protein deacetylation, producing O-acetyl-ADP-ribose and nicotinamide as well as the deacetylated protein. NAD+ is an important player and factor to research metabolic pathways and pathologies.
  • SMILES
    O[C@H]1C(N2C=NC3=C2N=CN=C3N)O[C@H](COP(O)(OP(OC[C@@H]4[C@@H](O)[C@@H](O)[C@@H]([N+]5=CC(C(N)=O)=CC=C5)O4)([O-])=O)=O)[C@H]1O
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200