Description
Chemical Identity & Molecular Composition
Chemical Name: Nicotinamide Adenine Dinucleotide (Oxidized Form, NAD⁺)
Chemical Class: Pyridine nucleotide coenzyme
Molecular Formula: C₂₁H₂₇N₇O₁₄P₂
Molecular Weight: ~663.43 g/mol
CAS Number: 53-84-9
Structural Characteristics
Nicotinamide adenine dinucleotide (NAD⁺) is a naturally occurring dinucleotide composed of two nucleotides joined through their phosphate groups—one containing an adenine base and the other containing nicotinamide. The molecule exists in an oxidized (NAD⁺) and reduced (NADH) redox pair, enabling reversible electron transfer in biochemical systems.
The nicotinamide moiety serves as the redox-active center, while the adenine ribose phosphate provides structural stability and enzyme recognition. NAD⁺ is water-soluble and commonly supplied as a lyophilized powder for controlled in vitro research applications.
Biochemical Function & Mechanistic Activity (Research Context Only)
Redox Coenzyme Activity
In vitro research utilizes NAD⁺ as a central electron carrier in oxidation–reduction reactions. NAD⁺ accepts electrons to form NADH, facilitating enzymatic studies of metabolic and energy-related pathways.
Enzyme Cofactor Function
NAD⁺ functions as a required cofactor in laboratory studies involving dehydrogenases, oxidoreductases, and other NAD⁺-dependent enzymes.
Substrate for NAD⁺-Consuming Enzymes
Researchers investigate NAD⁺ as a substrate in cellular signaling studies involving sirtuins, poly(ADP-ribose) polymerases (PARPs), and NAD⁺-dependent deacetylation and ADP-ribosylation reactions under controlled laboratory conditions.
Cellular Metabolism Models
In vitro systems use NAD⁺ to study cellular redox balance, metabolic flux, and energy-related biochemical pathways. All findings are limited to non-clinical laboratory research and do not imply therapeutic use.
Research Applications
NAD⁺ is commonly used in laboratory studies to investigate:
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Redox reactions and electron transfer mechanisms
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Enzyme kinetics involving NAD⁺-dependent oxidoreductases
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Cellular metabolism and energy-related biochemical pathways
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Sirtuin and PARP enzymatic activity (in vitro)
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Redox balance and coenzyme cycling
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Structure-function relationships of pyridine nucleotides
All applications are intended strictly for non-clinical, in vitro research use only.
Product Specifications
Form & Stability
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Format: Lyophilized nucleotide coenzyme
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Purity: ≥ 98% (HPLC validated)
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Appearance: White to off-white crystalline or lyophilized powder
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Solubility: Readily soluble in water and compatible laboratory buffers
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Stability: Stable in lyophilized form; sensitive to moisture, heat, and light after reconstitution
Storage
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Store at –20°C
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Protect from light and humidity
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Avoid repeated freeze–thaw cycles
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Use aseptic laboratory handling procedures
Packaging
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Provided in sterile, sealed vials
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Labeled with batch number, lot, purity, and molecular identification
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Manufactured under controlled laboratory conditions to ensure research-grade consistency
Composition
Each vial contains:
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5 mg, 10 mg, or 20 mg of high-purity Nicotinamide Adenine Dinucleotide (NAD⁺)
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No fillers, additives, or excipients
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Lyophilized to maintain molecular stability and reproducible research outcomes
Intended Use
This compound is intended exclusively for laboratory research, including:
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Redox and electron-transfer studies
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Enzyme kinetics and cofactor dependency assays
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Cellular metabolism and biochemical pathway research
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NAD⁺-dependent enzymatic mechanism studies
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Structure-function analysis of nucleotide coenzymes
Not for human or animal consumption, medical, therapeutic, cosmetic, or diagnostic applications.
Research-Only Disclaimer
This product is strictly for research use only. It is NOT intended for:
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Human or animal consumption
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Therapeutic, cosmetic, or wellness use
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Clinical or diagnostic applications
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In vivo studies
Proper laboratory handling procedures and safety protocols are required.
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