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  3. Puromycin

Puromycin dihydrochloride is the dihydrochloride salt of puromycin. Puromycin is an aminoglycoside antibiotic that inhibits protein synthesis.

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

Puromycin Chemical Structure

Puromycin Chemical Structure

CAS No. : 53-79-2

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 241 publication(s) in Google Scholar

Other Forms of Puromycin:

Top Publications Citing Use of Products

238 Publications Citing Use of MCE Puromycin

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WB

    Puromycin purchased from MedChemExpress. Usage Cited in: Autophagy. 2025 Jan 6.  [Abstract]

    Wild-type or mutated A549 cells subjected to the indicated treatments were stably transfected with puromycin dihydrochloride-inducible stubRFP-sensGFP-LC3 at an MOI of 5 (scale bar: 10 μm).

    Puromycin purchased from MedChemExpress. Usage Cited in: Mol Cell. 2023 Nov 24:S1097-2765(23)00911-5.  [Abstract]

    Global protein synthesis analyzed by puromycin dihydrochloride (4 d) labeling assay upon METTL14 knockdown in HeLa cells. Silencing of EIF3A serves as a positive control.

    Puromycin purchased from MedChemExpress. Usage Cited in: Mol Cell. 2023 Nov 24:S1097-2765(23)00911-5.  [Abstract]

    Global protein synthesis analyzed by puromycin dihydrochloride (4 d) labeling assay upon IGF2BP1-3 knockdown in HeLa cells.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Puromycin dihydrochloride is the dihydrochloride salt of puromycin. Puromycin is an aminoglycoside antibiotic that inhibits protein synthesis.

    IC50 & Target

    Aminoglycoside

     

    Cellular Effect
    Cell Line Type Value Description References
    A549 IC50
    300 nM
    Compound: 5
    Cytotoxicity against human A549 cells assessed as decrease in cell viability after 48 hrs
    Cytotoxicity against human A549 cells assessed as decrease in cell viability after 48 hrs
    [PMID: 30418763]
    HEK293 CC50
    0.23 μM
    Compound: Puromycin
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability measured after 48 hrs by resazurin assay
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability measured after 48 hrs by resazurin assay
    [PMID: 33479668]
    HEK293 IC50
    0.35 nM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells by alamar blue assay
    Cytotoxicity against HEK293 cells by alamar blue assay
    [PMID: 27212070]
    HEK293 IC50
    0.36 μM
    Compound: Puromycin
    Growth inhibition of HEK293 cells after 72 hrs by PrestoBlue staining based fluorescence assay
    Growth inhibition of HEK293 cells after 72 hrs by PrestoBlue staining based fluorescence assay
    [PMID: 28001067]
    HEK293 IC50
    0.361 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells assessed as cell viability after 72 hrs by resazurin-based plate reader analysis
    Cytotoxicity against HEK293 cells assessed as cell viability after 72 hrs by resazurin-based plate reader analysis
    [PMID: 26651537]
    HEK293 IC50
    0.4 μM
    Compound: Puromycin
    Cytotoxicity against human HEK293 cells after 72 hrs by resazurin dye based fluorescence assay
    Cytotoxicity against human HEK293 cells after 72 hrs by resazurin dye based fluorescence assay
    [PMID: 29969262]
    HEK293 IC50
    0.42 μM
    Compound: Puromycin
    Cytotoxicity against HEK239 cells after 72 hrs by Alamar blue assay
    Cytotoxicity against HEK239 cells after 72 hrs by Alamar blue assay
    [PMID: 20558060]
    HEK293 IC50
    0.45 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye based assay
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye based assay
    [PMID: 29236492]
    HEK293 IC50
    0.46 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by alamar blue assay
    Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by alamar blue assay
    [PMID: 29533611]
    HEK293 IC50
    0.46 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells assessed as cell growth inhibition after 72 hrs by Alamar blue assay
    Cytotoxicity against HEK293 cells assessed as cell growth inhibition after 72 hrs by Alamar blue assay
    [PMID: 28774427]
    HEK293 IC50
    0.6645 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells assessed as inhibition of cell growth incubated for 72 hrs by alamar blue dye based fluorescence assay
    Cytotoxicity against HEK293 cells assessed as inhibition of cell growth incubated for 72 hrs by alamar blue dye based fluorescence assay
    [PMID: 36799121]
    HEK293 IC50
    0.694 μM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye-based fluorescence assay
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye-based fluorescence assay
    [PMID: 30865443]
    HEK293 IC50
    0.81 μM
    Compound: Puromycin
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability after 72 hrs by resazurin dye based assay
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability after 72 hrs by resazurin dye based assay
    [PMID: 33105995]
    HEK293 IC50
    350.5 nM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells assessed as growth inhibition after 72 hrs by alamar blue viability assay
    Cytotoxicity against HEK293 cells assessed as growth inhibition after 72 hrs by alamar blue viability assay
    [PMID: 27060763]
    HEK293 CC50
    500.1 nM
    Compound: Puromycin
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye based assay
    Cytotoxicity against HEK293 cells after 72 hrs by resazurin dye based assay
    [PMID: 30537832]
    HEK-293T CC50
    0.42 μM
    Compound: Puromycin
    Cytotoxicity against human HEK293T cells assessed as decrease in cell viability after 72 hrs by CellTiter-Glo reagent based luminescence assay
    Cytotoxicity against human HEK293T cells assessed as decrease in cell viability after 72 hrs by CellTiter-Glo reagent based luminescence assay
    [PMID: 29469575]
    HepG2 IC50
    0.23 μM
    Compound: puromycin
    Growth inhibition of human HepG2 cells after 72 hrs by MTT assay
    Growth inhibition of human HepG2 cells after 72 hrs by MTT assay
    [PMID: 18313307]
    HepG2 CC50
    0.83 μM
    Compound: Puromycin
    Cytotoxicity against human HepG2 cells assessed as decrease in cell viability after 72 hrs by CellTiter-Glo reagent based luminescence assay
    Cytotoxicity against human HepG2 cells assessed as decrease in cell viability after 72 hrs by CellTiter-Glo reagent based luminescence assay
    [PMID: 29469575]
    HepG2 IC50
    2.1 x 10-1 μM
    Compound: puromycin
    Growth inhibition of human HepG2 cells after 72 hrs by SRB assay
    Growth inhibition of human HepG2 cells after 72 hrs by SRB assay
    [PMID: 18512984]
    HepG2 IC50
    83.93 μM
    Compound: puromycin
    Growth inhibition of doxorubicin resistant human HepG2 cells after 72 hrs by MTT assay
    Growth inhibition of doxorubicin resistant human HepG2 cells after 72 hrs by MTT assay
    [PMID: 18313307]
    HL-60 EC50
    0.055 μM
    Compound: 1
    Antiproliferative activity against human HL60 cells after 72 hrs by MTT assay
    Antiproliferative activity against human HL60 cells after 72 hrs by MTT assay
    [PMID: 28803047]
    J774.A1 IC50
    10 μM
    Compound: Puromycin
    Cytotoxicity against mouse J774A1 cells by trypan blue exclusion assay
    Cytotoxicity against mouse J774A1 cells by trypan blue exclusion assay
    [PMID: 22934636]
    K562 IC50
    0.22 μM
    Compound: puromycin
    Growth inhibition of human K562 cells after 72 hrs by SRB assay
    Growth inhibition of human K562 cells after 72 hrs by SRB assay
    [PMID: 18313307]
    K562 IC50
    26.83 μM
    Compound: puromycin
    Growth inhibition of doxorubicin-resistant human K562 cells after 72 hrs by SRB assay
    Growth inhibition of doxorubicin-resistant human K562 cells after 72 hrs by SRB assay
    [PMID: 18313307]
    KB 3-1 IC50
    0.21 μM
    Compound: puromycin
    Growth inhibition of human KB3-1 cells after 72 hrs by MTT assay
    Growth inhibition of human KB3-1 cells after 72 hrs by MTT assay
    [PMID: 18313307]
    KB-V1 IC50
    79.3 μM
    Compound: puromycin
    Growth inhibition of human KB V1 cells after 72 hrs by MTT assay
    Growth inhibition of human KB V1 cells after 72 hrs by MTT assay
    [PMID: 18313307]
    MDA-MB-231 CC50
    0.48 μM
    Compound: Puromycin
    Cytotoxicity against human MDA-MB-231 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    Cytotoxicity against human MDA-MB-231 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    [PMID: 28523103]
    MIA PaCa-2 CC50
    0.2 μM
    Compound: Puromycin
    Cytotoxicity against human MIAPaCa2 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    Cytotoxicity against human MIAPaCa2 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    [PMID: 28523103]
    MOLT-4 EC50
    0.17 μM
    Compound: 1
    Antiproliferative activity against human MOLT4 cells after 72 hrs by MTT assay
    Antiproliferative activity against human MOLT4 cells after 72 hrs by MTT assay
    [PMID: 28803047]
    PC-3 IC50
    300 nM
    Compound: 5
    Cytotoxicity against human PC3 cells assessed as decrease in cell viability after 48 hrs
    Cytotoxicity against human PC3 cells assessed as decrease in cell viability after 48 hrs
    [PMID: 30418763]
    SU-DHL10 CC50
    0.11 μM
    Compound: Puromycin
    Cytotoxicity against human SU-DHL10 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    Cytotoxicity against human SU-DHL10 cells assessed as growth inhibition after 72 hrs by CellTitre-Glo luminescent assay
    [PMID: 28523103]
    Vero CC50
    2.8 μM
    Compound: 1
    Cytotoxicity against African green monkey Vero cells assessed as reduction in cell proliferation after 72 hrs by MTT assay
    Cytotoxicity against African green monkey Vero cells assessed as reduction in cell proliferation after 72 hrs by MTT assay
    [PMID: 28803047]
    In Vitro

    Puromycin blocks protein synthesis after aminoacyl-sRNA formation, and at the same time it leads to the accumulation of small peptides. Both of these effects appear to be due to the splitting of ribosome-bound peptidyl-sRNA,4 which results in release of incomplete peptide chains.[1]. Puromycin, an analog of the 3' end of aminoacyl-tRNA, causes premature termination of translation by being linked non-specifically to growing polypeptide chains. Puromycin has two modes of inhibitory action. The first is by acting as an acceptor substrate which attacks peptidyl-tRNA in the P site to form a nascent peptide. The second is by competing with aminoacyl-tRNA for binding to the A' site[2]. When used in minimal amounts, puromycin incorporation in neosynthesized proteins reflects directly the rate of mRNA translation in vitro. Puromycin immunodetection is an advantageous alternative to radioactive amino acid labeling. It allows the direct evaluation of translation activity in single cells by immunofluorescence microscopy and in heterogenous populations of cells by fluorescenceactivated cell sorting[3].

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

    Molecular Weight

    471.51

    Formula

    C22H29N7O5

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    OC[C@@H]1[C@@H](NC([C@@H](N)CC2=CC=C(OC)C=C2)=O)[C@H]([C@H](N3C=NC4=C3N=CN=C4N(C)C)O1)O

    Shipping

    Room temperature in continental US; may vary elsewhere.

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

    DMSO : 100 mg/mL (212.08 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 1 mg/mL (2.12 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.1208 mL 10.6042 mL 21.2085 mL
    5 mM 0.4242 mL 2.1208 mL 4.2417 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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * 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)

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

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

    Dosage

    mg/kg

    Animal weight
    (per animal)

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    Dosing volume
    (per animal)

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    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: 99.55%

    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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    H2O / DMSO 1 mM 2.1208 mL 10.6042 mL 21.2085 mL 53.0211 mL
    DMSO 5 mM 0.4242 mL 2.1208 mL 4.2417 mL 10.6042 mL
    10 mM 0.2121 mL 1.0604 mL 2.1208 mL 5.3021 mL
    15 mM 0.1414 mL 0.7069 mL 1.4139 mL 3.5347 mL
    20 mM 0.1060 mL 0.5302 mL 1.0604 mL 2.6511 mL
    25 mM 0.0848 mL 0.4242 mL 0.8483 mL 2.1208 mL
    30 mM 0.0707 mL 0.3535 mL 0.7069 mL 1.7674 mL
    40 mM 0.0530 mL 0.2651 mL 0.5302 mL 1.3255 mL
    50 mM 0.0424 mL 0.2121 mL 0.4242 mL 1.0604 mL
    60 mM 0.0353 mL 0.1767 mL 0.3535 mL 0.8837 mL
    80 mM 0.0265 mL 0.1326 mL 0.2651 mL 0.6628 mL
    100 mM 0.0212 mL 0.1060 mL 0.2121 mL 0.5302 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:
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    Cat. No.:
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