1. Anti-infection
  2. Bacterial Antibiotic Parasite
  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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1 mg USD 88 In-stock
5 mg USD 221 In-stock
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Customer Review

Based on 191 publication(s) in Google Scholar

Other Forms of Puromycin:

Top Publications Citing Use of Products

191 Publications Citing Use of MCE Puromycin

  • 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)

Mass
=
Concentration
×
Volume
×
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 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: 99.55%

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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Help & FAQs
  • Do most proteins show cross-species activity?

    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:
Puromycin
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HY-B1743
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