Cas no 3080-29-3 (L-Adenosine)

L-Adenosine is a naturally occurring nucleoside composed of adenine and D-ribose, playing a critical role in biochemical processes such as energy transfer (ATP/ADP cycling) and signal transduction (cAMP pathways). It serves as a precursor for nucleic acid synthesis and is integral to cellular metabolism. This high-purity compound is widely utilized in research applications, including enzymology, molecular biology, and pharmacological studies. Its advantages include high stability, well-characterized properties, and compatibility with enzymatic assays. L-Adenosine is particularly valuable for investigating adenosine receptor interactions and metabolic pathways, offering researchers a reliable standard for experimental reproducibility. Available in various grades, it meets stringent quality requirements for scientific use.
L-Adenosine structure
L-Adenosine structure
Product Name:L-Adenosine
CAS No:3080-29-3
MF:C10H13N5O4
MW:267.241321325302
MDL:MFCD01075784
CID:43784
PubChem ID:448374
Update Time:2025-06-08

L-Adenosine Chemical and Physical Properties

Names and Identifiers

    • (2S,3S,4R,5S)-2-(6-Amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
    • beta-L-Adenosine
    • L-ADENOSINE
    • 2-(6-aminopurin-9-yl)-5-methylol-tetrahydrofuran-3,4-diol
    • 2-(6-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
    • β-L-ADENOSINE
    • 9H-Purin-6-amine, 9-beta-L-ribofuranosyl-
    • Oprea1_180751
    • 9-beta-L-Ribofuranosyladenine
    • 9-(b-L-Ribofuranosyl)adenine
    • BDBM82533
    • SBB057547
    • 9-beta-L-Ribofuranosyl-9H-purine-6-amine
    • (2S,3S,4R,5S)-2-(6-aminopurin-9-yl)-5-(hydroxymeth
    • MFCD01075784
    • (2S,3S,4R,5S)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
    • AKOS022186150
    • SCHEMBL329845
    • W16174
    • FE0ACFBC-F7F2-426A-89CC-682E8EAF057C
    • (2S,3S,4R,5S)-2-(6-Amino-purin-9-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol
    • 3080-29-3 , L-Adenosine
    • NSC87676; -L-Adenosine
    • OIRDTQYFTABQOQ-DEGSGYPDSA-N
    • CAS_3080-29-3
    • 3080-29-3
    • (2S,3S,4R,5S)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
    • A876092
    • AS-63680
    • J-700332
    • (2S,3S,4R,5S)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
    • 9-(?-L-Ribofuranosyl)adenine
    • NA06227
    • L-Adenosine
    • MDL: MFCD01075784
    • Inchi: 1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6-,7-,10-/m0/s1
    • InChI Key: OIRDTQYFTABQOQ-DEGSGYPDSA-N
    • SMILES: O1[C@@H](CO)[C@@H]([C@@H]([C@H]1N1C=NC2C(N)=NC=NC1=2)O)O

Computed Properties

  • Exact Mass: 267.09700
  • Monoisotopic Mass: 267.097
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 2
  • Complexity: 335
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -1.1
  • Topological Polar Surface Area: 140

Experimental Properties

  • Density: 2.085
  • Melting Point: 257.0-257.5 deg C (0.4 H2O)
  • Boiling Point: 676.271 °C at 760 mmHg
  • Flash Point: 362.796 °C
  • PSA: 139.54000
  • LogP: -1.39880

L-Adenosine Security Information

L-Adenosine Pricemore >>

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abcr
AB510981-250 mg
(2S,3S,4R,5S)-2-(6-Amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol; .
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abcr
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L-Adenosine Suppliers

Amadis Chemical Company Limited
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(CAS:3080-29-3)L-Adenosine
Order Number:A876092
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 09:48
Price ($):419.0
NewCan Biotech Limited
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(CAS:3080-29-3)L-Adenosine
Order Number:NC12090
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Quantity:10g
Purity:97%
Pricing Information Last Updated:Friday, 18 July 2025 16:07
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Additional information on L-Adenosine

L-Adenosine (CAS No. 3080-29-3): A Comprehensive Overview

L-Adenosine, also known as adenosine, is a naturally occurring nucleoside that plays a crucial role in various physiological processes. With the chemical formula C10H13N5O4, it is identified by the CAS number 3080-29-3. This compound is composed of adenine, a purine base, and ribose, a pentose sugar. Adenosine is widely recognized for its involvement in energy metabolism, neurotransmission, and cardiovascular regulation.

In the context of energy metabolism, adenosine is a key component of adenosine triphosphate (ATP), the primary energy currency of cells. ATP is generated through cellular respiration and is essential for numerous biological processes, including muscle contraction, nerve impulse propagation, and biosynthesis. The breakdown of ATP to adenosine and inorganic phosphate (Pi) releases energy that can be harnessed by cells to perform various functions.

Adenosine also functions as an important neuromodulator in the central nervous system (CNS). It acts on specific adenosine receptors (A1, A2A, A2B, and A3) to modulate neurotransmitter release and neuronal activity. For instance, activation of A1 receptors generally leads to inhibitory effects, reducing neuronal firing and promoting sleep. Conversely, activation of A2A receptors can have excitatory effects, enhancing neurotransmitter release and synaptic plasticity.

In the cardiovascular system, adenosine exerts potent vasodilatory effects by relaxing smooth muscle cells in blood vessels. This action helps to regulate blood flow and maintain cardiovascular homeostasis. Adenosine is also involved in the regulation of heart rate and contractility, making it a valuable therapeutic target for conditions such as angina pectoris and myocardial infarction.

The therapeutic potential of adenosine has been extensively explored in clinical settings. In cardiology, adenosine is used as a diagnostic agent for stress testing to assess coronary artery disease. It is also employed as an antiarrhythmic agent to terminate supraventricular tachycardia (SVT) by slowing conduction through the atrioventricular (AV) node. Additionally, adenosine has been investigated for its anti-inflammatory properties and potential applications in treating inflammatory diseases.

Recent research has shed light on the multifaceted roles of adenosine in various diseases. For example, studies have shown that adenosine signaling pathways are dysregulated in neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease. Modulating these pathways with adenosine receptor agonists or antagonists may offer new therapeutic strategies for these conditions.

In cancer research, adenosine has been implicated in tumor progression and immune evasion. Tumor cells can release high levels of adenosine into the microenvironment, which can suppress immune cell function and promote tumor growth. Targeting adenosine signaling with specific inhibitors or modulators may enhance the efficacy of cancer immunotherapies.

The pharmacological properties of adenosine have also been studied in the context of pain management. Adenosine receptors are expressed in nociceptive pathways, and activation of these receptors can produce analgesic effects. This has led to the development of novel adenosine-based analgesics that may provide alternative options for pain relief.

In conclusion, L-Adenosine (CAS No. 3080-29-3) is a versatile compound with significant biological importance and therapeutic potential. Its roles in energy metabolism, neurotransmission, cardiovascular regulation, and disease pathogenesis highlight its relevance across multiple fields of research and clinical practice. Ongoing studies continue to uncover new insights into the mechanisms underlying adenosine's actions, paving the way for innovative therapeutic approaches.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:3080-29-3)L-Adenosine
A876092
Purity:99%
Quantity:5g
Price ($):419.0
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NewCan Biotech Limited
(CAS:3080-29-3)L-Adenosine
NC12090
Purity:97%
Quantity:10g
Price ($):Inquiry
Email