Cas no 73-03-0 (Cordycepin)

Cordycepin (3'-deoxyadenosine) is a bioactive nucleoside analog derived from Cordyceps fungi, exhibiting notable pharmacological properties. Its structural similarity to adenosine enables interference with RNA synthesis, contributing to its broad-spectrum biological activities. Key advantages include potent anti-inflammatory, immunomodulatory, and antitumor effects, supported by mechanisms such as inhibition of polyadenylation and mTOR signaling pathways. Cordycepin also demonstrates neuroprotective and cardioprotective potential, with research highlighting its role in attenuating oxidative stress and apoptosis. Its bioavailability and metabolic stability are areas of ongoing optimization. As a research compound, Cordycepin serves as a valuable tool for studying nucleotide metabolism and developing therapeutic interventions.
Cordycepin structure
Cordycepin structure
Product Name:Cordycepin
CAS No:73-03-0
MF:C10H13N5O3
MW:251.241921186447
MDL:MFCD00037998
CID:33946
PubChem ID:24892611
Update Time:2025-08-14

Cordycepin Chemical and Physical Properties

Names and Identifiers

    • Cordycepin
    • 3'-DEOXYADENOSINE
    • 3’-deoxy-adenosin
    • 9-cordyceposidoadenine
    • cordycepin crystalline
    • 9-(3-Deoxy-b-D-erythro-pentofuranosyl)-9H-purin-6-amine
    • 9-(3-Deoxy-b-D-ribofuranosyl)adenine
    • Cordycepin from Cordyceps militaris
    • CORDYCEPIN(RG)
    • (-)-cordycepin
    • 3'-Deoxy-D-adenosine
    • Adenine cordyceposide
    • Adenosine,3-deoxy
    • Cordycepin Hydrate
    • Cordyceps fungus powder
    • 3'-Deoxyadenosine from Cordyceps militaris
    • 3′-Deoxyadenosine
    • Cordycepine
    • ADENOSINE, 3'-DEOXY-
    • 9-(beta-D-3'-Deoxyribofuranosyl)adenine
    • 9H-Purine, 6-amino-9-(3-deoxy-beta-D-ribofuranosyl)-
    • GZ8VF4M2J8
    • OFEZSBMBBKLLBJ-BAJZRUMYSA-N
    • beta-D-erythro-Pentofuranoside, adenine-9 3-deoxy-
    • 9H-Purin-6-amine, 9-(3-deoxy-beta-D-erythro-pentofuranosyl)-
    • (2R,3R,5S)-2-(6-amino-9H-purin-9-yl)-5-(hydroxy
    • 3-Deoxyadenosine
    • BDBM50031231
    • 9-(.beta.-D-3'-Deoxyribofuranosyl)adenine
    • MLS003389401
    • NSC-627047
    • CHEMBL42814
    • 3'-Deoxyadenosine (cordycepin)
    • 3-Deoxyadenosine; 9(3DeoxyDribofuranosyl)adenine;3Deoxyadenosine
    • BCP01713
    • HMS3372P05
    • 9H-Purin-6-amine, 9-(3-deoxy-.beta.-D-erythro-pentofuranosyl)-
    • 5''-deoxyadenosine2-(6-Amino-purin-9-yl)-5-hydroxymethyl-tetrahydro-furan-3-ol
    • NSC-89220
    • NSC401022
    • SMR002049054
    • BRD2581
    • NSC63984
    • 9-(3-deoxypentofuranosyl)-9h-purin-6-amine
    • SY077107
    • BRD-A61362581-001-02-0
    • SCHEMBL20419171
    • BRD-A61362581-001-01-2
    • DTXSID00859090
    • 2-(6-aminopurin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3-ol
    • HMS3268J08
    • 2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolan-3-ol
    • .beta.-D-erythro-Pentofuranoside, adenine-9 3-deoxy-
    • NCI60_013263
    • NSC89220
    • BRD-2581
    • 9H-Purine, 6-amino-9-(3-deoxy-.beta.-D-ribofuranosyl)-
    • NSC627047
    • OFEZSBMBBKLLBJ-UHFFFAOYSA-N
    • 3 inverted exclamation mark -Deoxyadenosine
    • 2-(6-Amino-purin-9-yl)-5-hydroxymethyl-tetrahydro-furan-3-ol
    • SB18953
    • MLSMR
    • MDL: MFCD00037998
    • Inchi: 1S/C10H13N5O3/c11-8-7-9(13-3-12-8)15(4-14-7)10-6(17)1-5(2-16)18-10/h3-6,10,16-17H,1-2H2,(H2,11,12,13)
    • InChI Key: OFEZSBMBBKLLBJ-UHFFFAOYSA-N
    • SMILES: O1C(CO)CC(C1N1C=NC2C(N)=NC=NC1=2)O
    • BRN: 0035194

Computed Properties

  • Exact Mass: 251.10200
  • Monoisotopic Mass: 251.10183929 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 307
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Molecular Weight: 251.24
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: -1.2
  • Topological Polar Surface Area: 119

Experimental Properties

  • Color/Form: Powder
  • Density: 1.2938 (rough estimate)
  • Melting Point: 224.0 to 228.0 deg-C
  • Boiling Point: 627.2℃ at 760 mmHg
  • Flash Point: 333.1 °C
  • Refractive Index: 1.7610 (estimate)
  • PSA: 119.31000
  • LogP: -0.36960
  • Merck: 2529
  • Specific Rotation: D20 -47°; D27 -42°
  • λmax: 260(EtOH)(lit.)
  • Solubility: Soluble in water.

Cordycepin Security Information

  • Symbol: GHS06
  • Prompt:warning
  • Signal Word:Danger
  • Hazard Statement: H301,H315,H319,H335
  • Warning Statement: P261,P301+P310,P305+P351+P338
  • Hazardous Material transportation number:UN 2811
  • WGK Germany:3
  • Hazard Category Code: R25;R36/37/38
  • Safety Instruction: S26-S45
  • FLUKA BRAND F CODES:10-21
  • RTECS:AU7358610
  • Hazardous Material Identification: T
  • Risk Phrases:R25; R36/37/38
  • Safety Term:S26;S45
  • HazardClass:6.1
  • Storage Condition:Powder -20°C 3 years In solvent -80°C 6 months ? -20°C 1 month

Cordycepin Customs Data

  • HS CODE:29349990
  • Customs Data:

    China Customs Code:

    2934999090

    Overview:

    2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Cordycepin Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd
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Cordycepin Spectrogram

13C NMR
13C NMR
1H NMR 300 MHz DMSO
1H NMR
MS-MS
MS-MS

Additional information on Cordycepin

Introduction to Cordycepin (CAS No. 73-03-0) and Its Recent Research Findings

Cordycepin, chemically known as 3′-hydroxyadenine, is a naturally occurring nucleoside derivative found primarily in certain species of the Cordyceps fungus. With a CAS number of 73-03-0, this compound has garnered significant attention in the field of pharmaceutical research due to its unique biological properties and potential therapeutic applications. This article provides an in-depth exploration of Cordycepin, highlighting its chemical structure, pharmacological effects, and the latest research findings that underscore its significance in modern medicine.

The chemical structure of Cordycepin closely resembles that of adenosine, a naturally occurring nucleoside essential for cellular metabolism. However, Cordycepin features a hydroxyl group at the 3′ position of the ribose sugar, which distinguishes it from adenosine. This structural modification imparts distinct pharmacological activities, making Cordycepin a subject of extensive scientific investigation. The compound is known for its potent biological effects, including anti-inflammatory, antioxidant, and anticancer properties, which have been the focus of numerous preclinical and clinical studies.

One of the most compelling aspects of Cordycepin is its ability to modulate various cellular pathways involved in cancer progression. Recent studies have demonstrated that Cordycepin can induce apoptosis (programmed cell death) in cancer cells while sparing healthy cells. This selective toxicity is attributed to its ability to inhibit enzymes such as adenosine deaminase (ADA) and deoxyhypusine synthase (DHS), which are crucial for cancer cell survival. Additionally, Cordycepin has been shown to disrupt tumor blood vessel formation (angiogenesis), further inhibiting cancer growth and metastasis.

In the realm of immunomodulation, Cordycepin has emerged as a promising immunostimulant. Research indicates that it can enhance the activity of natural killer (NK) cells and T-lymphocytes, key components of the immune system responsible for identifying and destroying pathogens. These findings suggest that Cordycepin may be beneficial in treating immunodeficient conditions and enhancing vaccine efficacy. Furthermore, studies have explored its potential role in managing chronic inflammatory diseases by suppressing pro-inflammatory cytokines such as TNF-α and IL-6.

The antioxidant properties of Cordycepin have also been extensively studied. Oxidative stress, resulting from an imbalance between free radicals and antioxidants, is implicated in various chronic diseases, including neurodegenerative disorders like Alzheimer's disease and Parkinson's disease. Preclinical research has shown that Cordycepin can scavenge reactive oxygen species (ROS) and protect against oxidative damage in neuronal cells. These findings have opened new avenues for investigating Cordycepin as a potential therapeutic agent for neuroprotection.

Recent advances in clinical trials have provided further evidence of Cordycepin's therapeutic potential. A notable study published in a peer-reviewed journal demonstrated that Cordycepin, when combined with conventional chemotherapy, significantly improved outcomes in patients with certain types of cancer. The study reported reduced tumor burden and prolonged survival rates among participants receiving the combination therapy. While more research is needed to confirm these findings and establish optimal dosing regimens, these results are highly encouraging for future clinical applications.

The pharmacokinetics of Cordycepin have also been a focus of research efforts. Studies have shown that the compound exhibits moderate bioavailability upon oral administration but undergoes rapid metabolism in vivo. To enhance its therapeutic efficacy, researchers are exploring novel delivery systems such as nanoparticles and liposomes, which could improve drug delivery and target specificity. Additionally, investigations into the compound's mechanism of action at the molecular level are providing valuable insights into its interactions with cellular targets.

The natural sources of Cordycepin have also been a subject of interest. While traditionally sourced from fungal species like *Cordyceps militaris*, advancements in biotechnology have enabled synthetic production methods that are more sustainable and scalable. These developments not only ensure a consistent supply of high-quality Cordycepin but also reduce dependency on wild-cultivated sources, which may be subject to environmental variability and contamination risks.

In conclusion, Cordycepin (CAS No. 73-03-0) is a multifaceted compound with significant therapeutic potential across various medical conditions. Its unique chemical structure and biological activities make it a valuable candidate for further research and development. The latest findings from preclinical and clinical studies highlight its promise as an anticancer agent, immunomodulator, antioxidant, and neuroprotective compound. As research continues to uncover new applications for this remarkable natural product, it is poised to play an increasingly important role in modern medicine.

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Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:73-03-0)Cordycepin
LE939;LE10149;LE27030051
Purity:99%/99%/99%
Quantity:25KG,200KG,1000KG/25KG,200KG,1000KG/25KG,200KG,1000KG
Price ($):Inquiry/Inquiry/Inquiry
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Amadis Chemical Company Limited
(CAS:73-03-0)Cordycepin
A837698
Purity:99%/99%
Quantity:5g/25g
Price ($):262.0/917.0
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