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Adenosine  (Synonyms: Adenine riboside; D-Adenosine)

Cat. No.: HY-B0228 Purity: 99.96%
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Adenosine (Adenine riboside), a ubiquitous and BBB-permeable endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation.

For research use only. We do not sell to patients.

CAS No. : 58-61-7

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10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 18 publication(s) in Google Scholar

Other Forms of Adenosine:

Top Publications Citing Use of Products

    Adenosine purchased from MedChemExpress. Usage Cited in: Nature. 2026 Jan;649(8096):423-431.  [Abstract]

    a-c, Direct infusion of Adenosine into the mPFC produced sustained antidepressant-like effects. a, Experimental timeline and representative image of the bilateral infusion site in the mPFC of CRS. Scale bar, 500 µm. b,c, Immobility time in the forced swim test (FST; b) and sucrose preference (c) were measured 24 h after infusion of Adenosine (0.1 µg per side).

    Adenosine purchased from MedChemExpress. Usage Cited in: Diabetol Metab Syndr. 2025 May 24;17(1):164.  [Abstract]

    Weight changes in mice. Images of NFD mice, HFD mice, HS mice and HA mice (A); Trends in body weight of mice in NFD, HFD, HS and HA groups, quantitative analysis, n = 12 (B). Abbreviations: NFD, normal-fat diet; HFD, high-fat die; HS, HFD + semaglutide intervention; HA, HFD + Adenosine (20 mg/kg; i.p.; Once daily) intervention.

    Adenosine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2024 Jun 14:e2306514.  [Abstract]

    Adenosine (0.5-6 mg/kg; i.p.; single dose). ICPs and AUCs of adenosine receptor knock‐out (A1−/−, A2a−/−, A2b−/−, A3−/−) and WT mice. N = 8 in each group. Statistical analysis was performed using an unpaired t‐test. * P < 0.05, **** P < 0.0001.

    Adenosine purchased from MedChemExpress. Usage Cited in: Theranostics. 2024 Aug 12;14(12):4874-4893.  [Abstract]

    The percentages of CD25+, CD69+ and CD154+ activated CD4+ T cells among the untreated group (NA), control group (Ctrl) and ADO (Adenosine, 5 mM; 24 h) group.

    Adenosine purchased from MedChemExpress. Usage Cited in: Int J Mol Med. 2016 Sep;38(3):969-75.  [Abstract]

    Effects of Adenosine and CGS21680 on CD39 and CD73 expression. (A) Adenosine and CGS21680 promote the expression of CD39. (B) Adenosine and CGS21680 promote the expression of CD73. GAPDH is used as an internal reference.

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Adenosine (Adenine riboside), a ubiquitous and BBB-permeable endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2].

    IC50 & Target

    Human Endogenous Metabolite

     

    Microbial Metabolite

     

    Cellular Effect
    Cell Line Type Value Description References
    A-431 IC50
    195 μM
    Compound: Adenosine
    Inhibition of erbB-1 receptor tyrosine kinase from A431 human epidermoid carcinoma cells
    Inhibition of erbB-1 receptor tyrosine kinase from A431 human epidermoid carcinoma cells
    [PMID: 9089334]
    CHO EC50
    0.29 μM
    Compound: adenosine
    Agonist activity at human adenosine A3 receptor expressed in CHO cells assessed as increase of intracellular calcium level
    Agonist activity at human adenosine A3 receptor expressed in CHO cells assessed as increase of intracellular calcium level
    [PMID: 20541935]
    CHO EC50
    0.29 μM
    Compound: adenosine
    Agonist activity at human adenosine A3 receptor expressed in CHO cells
    Agonist activity at human adenosine A3 receptor expressed in CHO cells
    [PMID: 21388809]
    CHO EC50
    0.31 μM
    Compound: adenosine
    Agonist activity at human adenosine A1 receptor expressed in CHO cells assessed as increase of intracellular calcium level
    Agonist activity at human adenosine A1 receptor expressed in CHO cells assessed as increase of intracellular calcium level
    [PMID: 20541935]
    CHO EC50
    0.31 μM
    Compound: adenosine
    Agonist activity at human adenosine A1 receptor expressed in CHO cells
    Agonist activity at human adenosine A1 receptor expressed in CHO cells
    [PMID: 21388809]
    CHO EC50
    0.7 μM
    Compound: adenosine
    Agonist activity at human adenosine A2A receptor expressed in CHO cells assessed as increase of intracellular calcium level
    Agonist activity at human adenosine A2A receptor expressed in CHO cells assessed as increase of intracellular calcium level
    [PMID: 20541935]
    CHO EC50
    0.7 μM
    Compound: adenosine
    Agonist activity at human adenosine A2A receptor expressed in CHO cells
    Agonist activity at human adenosine A2A receptor expressed in CHO cells
    [PMID: 21388809]
    CHO EC50
    23500 nM
    Compound: AR-1
    Agonist activity at human adenosine A2B receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    Agonist activity at human adenosine A2B receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    [PMID: 26356532]
    CHO EC50
    24 μM
    Compound: adenosine
    Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as increase of intracellular calcium level
    Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as increase of intracellular calcium level
    [PMID: 20541935]
    CHO EC50
    24 μM
    Compound: adenosine
    Agonist activity at human adenosine A2B receptor expressed in CHO cells
    Agonist activity at human adenosine A2B receptor expressed in CHO cells
    [PMID: 21388809]
    CHO EC50
    290 nM
    Compound: AR-1
    Agonist activity at human adenosine A3 receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    Agonist activity at human adenosine A3 receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    [PMID: 26356532]
    CHO EC50
    310 nM
    Compound: AR-1
    Agonist activity at human adenosine A1 receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    Agonist activity at human adenosine A1 receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    [PMID: 26356532]
    CHO EC50
    730 nM
    Compound: AR-1
    Agonist activity at human adenosine A2A receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    Agonist activity at human adenosine A2A receptor transfected in CHO cells assessed as changes in cAMP formation in the presence of nitrobenzylthioinosine
    [PMID: 26356532]
    COS-7 EC50
    1.04 μM
    Compound: adenosine
    Activity against human wild type adenosine A3 receptor expressed in COS7 cells as measured by accumulation of inositol phosphate by PLC assay
    Activity against human wild type adenosine A3 receptor expressed in COS7 cells as measured by accumulation of inositol phosphate by PLC assay
    [PMID: 16640329]
    Detroit 98 ED50
    0.08 μM
    Compound: 2
    Concentration that inhibited the growth of cultured human detroit 98 cells.
    Concentration that inhibited the growth of cultured human detroit 98 cells.
    [PMID: 7131482]
    HEK-293T EC50
    0.039 μM
    Compound: Adenosine
    Agonist activity at human A1AR expressed in HEK293T/17 cells assessed as inhibition of isoproterenol-induced cAMP accumulation incubated for 10 mins by luciferase reporter assay
    Agonist activity at human A1AR expressed in HEK293T/17 cells assessed as inhibition of isoproterenol-induced cAMP accumulation incubated for 10 mins by luciferase reporter assay
    [PMID: 22738238]
    HEp-2 IC50
    0.7 μM
    Compound: 1
    Compound was evaluated for cytotoxicity against H.Ep.-2 cells, and concentration required to inhibit the growth of treated cells to 50% of untreated control.
    Compound was evaluated for cytotoxicity against H.Ep.-2 cells, and concentration required to inhibit the growth of treated cells to 50% of untreated control.
    [PMID: 6708054]
    HEp-2 IC50
    20 μM
    Compound: 1
    Compound was evaluated for cytotoxicity against H.Ep.-2 (AK-) cells and concentration required to inhibit the growth of treated cells to 50% of untreated control
    Compound was evaluated for cytotoxicity against H.Ep.-2 (AK-) cells and concentration required to inhibit the growth of treated cells to 50% of untreated control
    [PMID: 6708054]
    HeLa IC50
    10.8 μM
    Compound: 37
    Inhibition of cytopathogenicity of herpes simplex type 1 virus (HSV-1)(KOS) in Hela cell culture.
    Inhibition of cytopathogenicity of herpes simplex type 1 virus (HSV-1)(KOS) in Hela cell culture.
    [PMID: 7473592]
    HeLa IC50
    98.85 μM
    Compound: 37
    Concentration required to cause microscopically visible change or disruption in about 50% of Hela cell sheet.
    Concentration required to cause microscopically visible change or disruption in about 50% of Hela cell sheet.
    [PMID: 7473592]
    HepG2 IC50
    18.46 μM
    Compound: 35
    Inhibition of PCSK9 mRNA expression in human HepG2 cells by SYBR Green I dye-based qRT-PCR analysis
    Inhibition of PCSK9 mRNA expression in human HepG2 cells by SYBR Green I dye-based qRT-PCR analysis
    [PMID: 30448414]
    L1210 EC50
    1.869 mM
    Compound: 2
    Antitumor activity against mouse L1210 cells assessed as inhibition of [3H]thymidine incorporation after 72 hrs
    Antitumor activity against mouse L1210 cells assessed as inhibition of [3H]thymidine incorporation after 72 hrs
    [PMID: 24915876]
    L1210 IC50
    0.991 mM
    Compound: 2
    Cytotoxicity against mouse L1210 cells assessed as inhibition of cell viability after 72 hrs by MTT assay
    Cytotoxicity against mouse L1210 cells assessed as inhibition of cell viability after 72 hrs by MTT assay
    [PMID: 24915876]
    L929 ED50
    0.3 μM
    Compound: 2
    Concentration that inhibited the growth of Mouse L cells.
    Concentration that inhibited the growth of Mouse L cells.
    [PMID: 7131482]
    PBMC IC50
    1.867 mM
    Compound: 2
    Cytotoxicity against human PBMC assessed as inhibition of cell viability after 72 hrs by MTT assay
    Cytotoxicity against human PBMC assessed as inhibition of cell viability after 72 hrs by MTT assay
    [PMID: 24915876]
    RAW264.7 IC50
    > 10 μM
    Compound: 19
    Antiinflammatory activity in mouse RAW264.7 cells assessed as reduction in LPS-induced NO production pretreated for 30 mins followed by LPS stimulation for 24 hrs by Griess assay
    Antiinflammatory activity in mouse RAW264.7 cells assessed as reduction in LPS-induced NO production pretreated for 30 mins followed by LPS stimulation for 24 hrs by Griess assay
    [PMID: 28499733]
    U2OS EC50
    63 μM
    Compound: 60961
    Inhibition of the equilibrative nucleoside transporter (ENT1, SLC29A1) as assessed by GPCR-mediated changes in cell morphology using the impedance-based transporter activity through receptor activation (TRACT) assay (PubChem AID: 1745861)
    Inhibition of the equilibrative nucleoside transporter (ENT1, SLC29A1) as assessed by GPCR-mediated changes in cell morphology using the impedance-based transporter activity through receptor activation (TRACT) assay (PubChem AID: 1745861)
    [PMID: 31551431]
    In Vitro

    Adenosine (Adenine riboside) acts on four G-protein coupled receptors: two of them, A1 and A3, are primarily coupled to Gi family G proteins; and two of them, A2A and A2B, are mostly coupled to Gs like G proteins. These receptors are antagonized by xanthines including caffeine. Via these receptors it affects many cells and organs, usually having a cytoprotective function[2].
    Adenosine is an extracellular signaling molecule that is generated from its precursor molecules 5’-adenosine triphosphate (ATP) and 5’-adenosine monophosphate (AMP)[3].
    Adenosine is a common metabolite of ATP, which exhibits cytotoxic effects at high concentrations.Adenosine (1.0-4.0 mM; 12-24 hours) inhibits cell viability and triggers ER stress in HepG2 cells[4].
    Adenosine induces apoptosis in a variety of cancer cells. Adenosine (2.0 mM; 12-24 hours) induces autophagy in HepG2 cells. In HepG2 cell lines, Adenosine -induced AMPK/mTOR pathway activation partially blocked ER stress and decreased apoptotic cell death[4].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Clinical Trial
    Molecular Weight

    267.25

    Formula

    C10H13N5O4

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    NC1=C(N=CN2[C@H]3[C@H](O)[C@H](O)[C@@H](CO)O3)C2=NC=N1

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 1 year
    -20°C 6 months
    Solvent & Solubility
    In Vitro: 

    DMSO : 33.33 mg/mL (124.71 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 5 mg/mL (18.71 mM; ultrasonic and warming and heat to 60°C)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 3.7418 mL 18.7091 mL 37.4181 mL
    5 mM 0.7484 mL 3.7418 mL 7.4836 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    Mass
    =
    Concentration
    ×
    Volume
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    Molecular Weight *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    Volume (final)

    V2

    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 6.67 mg/mL (24.96 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    Purity & Documentation

    Purity: 99.96%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    H2O / DMSO 1 mM 3.7418 mL 18.7091 mL 37.4181 mL 93.5454 mL
    5 mM 0.7484 mL 3.7418 mL 7.4836 mL 18.7091 mL
    10 mM 0.3742 mL 1.8709 mL 3.7418 mL 9.3545 mL
    15 mM 0.2495 mL 1.2473 mL 2.4945 mL 6.2364 mL
    DMSO 20 mM 0.1871 mL 0.9355 mL 1.8709 mL 4.6773 mL
    25 mM 0.1497 mL 0.7484 mL 1.4967 mL 3.7418 mL
    30 mM 0.1247 mL 0.6236 mL 1.2473 mL 3.1182 mL
    40 mM 0.0935 mL 0.4677 mL 0.9355 mL 2.3386 mL
    50 mM 0.0748 mL 0.3742 mL 0.7484 mL 1.8709 mL
    60 mM 0.0624 mL 0.3118 mL 0.6236 mL 1.5591 mL
    80 mM 0.0468 mL 0.2339 mL 0.4677 mL 1.1693 mL
    100 mM 0.0374 mL 0.1871 mL 0.3742 mL 0.9355 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    Product Name:
    Adenosine
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