Cordycepin

SKU:BHB11900354
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Cordycepin is a research-grade small-molecule antagonist of Nucleoside supporting Cell Signaling and Epigenetics and Nuclear Signaling research. Supplied as a white powder with >98% purity (CAS 73-03-0, MW 251.2) dissolvable in DMSO; store at -20°C. For research use only.
Cas No. 73-03-0
Molecular Formula C10H13N5O3
Purity >98% (HPLC); NMR (Conforms)
Application Notes Nucleoside Antagonist
Options selector
Catalog no. Size
SIH-576-10MG 10 mg
SIH-576-50MG 50 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (2) — 10 mg, 50 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No SIH-576
Activity
  • Antagonist
Alternative Names (2R,3R,5S)-2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolan-3-ol; 3-deoxyadenosine; NSC 63984
Cas No. 73-03-0
Form White powder
Molecular Weight 251.2
Product Type
  • Biochemicals
  • Small Molecules
Purity >98% (HPLC); NMR (Conforms)
Shipping Shipped Ambient
SMILES NC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)C[C@H]3O
Solubility May be dissolved in DMSO (25 mg/ml)
Source Synthetic
Storage -20ºC

Cordycepin (3′-deoxyadenosine) is a naturally occurring adenosine analog that lacks a hydroxyl group at the 3′ position of its ribose moiety. This structural modification allows Cordycepin to interfere with RNA synthesis, polyadenylation, and cellular signaling pathways, making it a versatile molecule in biomedical research. In neuroscience, Cordycepin has garnered attention for its neuroprotective and anti-inflammatory properties, particularly in the context of neurodegenerative diseases.

Cordycepin has been shown to inhibit poly(ADP-ribose) polymerase 1 (PARP1), a key enzyme involved in DNA repair and cell death pathways. Overactivation of PARP1 is associated with neuronal damage in conditions such as Alzheimer’s and Parkinson’s disease. By modulating PARP1 activity, Cordycepin may help preserve neuronal integrity and reduce oxidative stress-induced apoptosis.

Additionally, Cordycepin exhibits anti-inflammatory effects by downregulating pro-inflammatory cytokines and signaling pathways, contributing to a reduction in neuroinflammation—a hallmark of many neurodegenerative disorders. It has also demonstrated the ability to inhibit beta-amyloid-induced apoptosis in hippocampal neurons, suggesting a direct protective effect against Alzheimer’s-related toxicity.

Beyond its neurological applications, Cordycepin has shown anti-cancer and anti-obesity activities, highlighting its broad therapeutic potential. However, its emerging role in modulating neuronal survival, inflammation, and protein aggregation positions it as a promising candidate for further exploration in neurodegenerative disease research.

Classification: Not a hazardous substance or mixture.

Safety Phrases:

  • S22 - Do not breathe dust.
  • S24/25 - Avoid contact with skin and eyes.
  • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.

Cordycepin (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-576)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. H Kim et al. Mol. Med. 2011 17:893
2. A Kondrashov et al. RNA 2012 18:2236
3. J Yang et al. Biomed. Pharmacother. 2017 95:1777
4. H Song et al. Neurotoxicology 2018 68:73
5. Y Zhang et al. OncoTargets Ther. 2018 11:4479
6. Y Li et al. Curr. Pharm. Des. 2018 Aug. 20, epub

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