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Research pen

AICAR Pen

Batch documentation
available on request
NORVEXA / Pen collectionIllustration
Documentation on request

5-Aminoimidazole-4-carboxamide ribonucleotide

AICAR (5-Aminoimidazole-4-carboxamide ribonucleotide) is a synthetic nucleotide analogue used in laboratory research to explore cellular pathways related to energy metabolism and AMP-activated protein kinase (AMPK) signalling.

Available strengths
Format
Pen
Selected reference
50 mg
Purity
Documentation on request
Documentation
Batch-specific COA on request
Also available as a vial Inquire about this reference Request batch documentation

For laboratory and research use only. Pen illustration is a visual reference. Confirm the supplied format and batch details with our team.

AICAR Pen, 50 mg selected.

A complete reference

The record matters.

Overview

AICAR (5-Aminoimidazole-4-carboxamide ribonucleotide) is a synthetic nucleotide analogue used in laboratory research to explore cellular pathways related to energy metabolism and AMP-activated protein kinase (AMPK) signalling.

AICAR is an intermediate compound associated with adenosine monophosphate (AMP) pathways. Within laboratory settings, it is commonly utilised as a tool compound in studies involving AMPK-related signalling mechanisms.

AICAR has been widely investigated in laboratory studies exploring metabolic signalling and cellular energy regulation. Areas of research interest include:

AMPK Activation Studies AICAR is frequently used in laboratory models investigating AMP-activated protein kinase signalling pathways.

Cellular Energy Regulation Researchers study how AICAR influences cellular energy sensing and metabolic communication pathways.

Metabolic Signalling Research Experimental studies explore the compound’s interaction with metabolic regulatory pathways.

Mitochondrial and Cellular Metabolism Studies AICAR is commonly examined in laboratory environments studying cellular metabolism and mitochondrial activity.

Chemical reference information: CAS number: 2627-69-2; Molecular formula: C₉H₁₄N₄O₅; Molecular weight: 258.23 g/mol. These reference identifiers describe the formulation; the batch-specific analytical record identifies the supplied material.

Reference conditions for unreconstituted research material are −20°C with moisture and direct light excluded. Use the storage instructions on the supplied batch record for the actual presentation, and record any change of physical state or storage conditions.

Where laboratory preparation is required, use an appropriate validated solvent and aseptic peptide-handling procedure. Solvent compatibility, final concentration, and post-preparation storage depend on the specific formulation and experimental protocol. The catalog strength is the compound amount, not the concentration of a prepared solution.

NORVEXA Bioscience batch documentation can be requested using the printed reference and lot number. Review identity, analytical purity, presentation, and handling specifications before including a material in a laboratory workflow.

AICAR 50 mg is offered as a NORVEXA research pen. The selected strength refers to the compound content of this pen reference. Request the matching batch record for identity, analytical specifications, and presentation details.

Handling and storage

Reference conditions for unreconstituted research material are −20°C with moisture and direct light excluded. Use the storage instructions on the supplied batch record for the actual presentation, and record any change of physical state or storage conditions.

Where laboratory preparation is required, use an appropriate validated solvent and aseptic peptide-handling procedure. Solvent compatibility, final concentration, and post-preparation storage depend on the specific formulation and experimental protocol. The catalog strength is the compound amount, not the concentration of a prepared solution.

NORVEXA Bioscience batch documentation can be requested using the printed reference and lot number. Review identity, analytical purity, presentation, and handling specifications before including a material in a laboratory workflow.

Scientific identifiers
CAS number
2627-69-2
Molecular formula
C₉H₁₄N₄O₅
Molecular weight
258.23 g/mol
Batch documentation

Include the printed batch reference when requesting your certificate of analysis. The record applies to the batch supplied to your laboratory.

Prepare a documentation request