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PUROMYCIN

Product Name
PUROMYCIN
CAS No.
53-79-2
Chemical Name
PUROMYCIN
Synonyms
achromycin;Stylomycin;1-mm;3123l;p-638;C01610;cl16536;cl13,900;nsc-3055;PUROMYCIN
CBNumber
CB7152906
Molecular Formula
C22H29N7O5
Formula Weight
471.51
MOL File
53-79-2.mol
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PUROMYCIN Property

Melting point:
175.5-177°
alpha 
D25 -11° (ethanol)
Boiling point:
572.65°C (rough estimate)
Density 
1.3119 (rough estimate)
refractive index 
1.7010 (estimate)
RTECS 
AU7350000
solubility 
DMF: Soluble
DMSO: Soluble
Ethanol: Soluble
Methanol: Soluble
pka
6.8, 7.2(at 25℃)
form 
Liquid
color 
White to off-white
Water Solubility 
Soluble in water (50 mg/ml at 20°C).
EPA Substance Registry System
Adenosine, 3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-N,N-dimethyl- (53-79-2)
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Safety

RIDADR 
3249
HazardClass 
6.1(b)
PackingGroup 
III
Toxicity
LD50 in mice (mg/kg): 350 i.v.; 525 i.p.; 675 orally (Porter, 1952)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P330Rinse mouth.

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N-Bromosuccinimide Price

TRC
Product number
P840325
Product name
Puromycin
Packaging
100mg
Price
$715
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0008744
Product name
PUROMYCIN
Purity
95.00%
Packaging
100MG
Price
$758.7
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0008744
Product name
PUROMYCIN
Purity
95.00%
Packaging
10MG
Price
$575.21
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0008744
Product name
PUROMYCIN
Purity
95.00%
Packaging
25MG
Price
$608.32
Updated
2021/12/16
DC Chemicals
Product number
DC10169
Product name
Puromycin
Purity
>98%
Packaging
250mg
Price
$600
Updated
2021/12/16
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PUROMYCIN Chemical Properties,Usage,Production

Description

Puromycin is an aminonucleoside antibiotic produced by Streptomyces alboniger. It is a very common antibiotic routinely used by scientists in biomedical research to select cells modified by genetic engineering. It specifically inhibits peptidyl transfer on both prokaryotic and eukaryotic ribosomes. The antibiotic inhibits the growth of Gram-positive bacteria and various animal and insect cells. Fungi and Gram-negative bacteria are resistant due to the low permeability of the antibiotic. For more than 30 years, puromycin has been widely used as a basic tool for studying protein synthesis. Now, puromycin hydrochloride is particularly useful for the selection of cell types harboring plasmids carrying puromycin resistance genes. Puromycinresistant cells express pac gene, which encodes an N-acetyl puromycin transferase. The pac gene can be mobilized on a plasmid and used to transfect a host cell in an attempt to provide resistance; therefore, puromycin can be used in gene selections for mammalian host cells.
This aminonucleoside antibiotic causes premature chain termination during translation in the ribosomes. Part of the molecule resembles the 30 end of the aminoacylated tRNA. It enters the A site and transfers to the growing chain, causing premature chain release. The exact mechanism of action is unknown, but the 30 position contains an amide linkage instead of the normal ester linkage of tRNA; the amide bond makes the molecule much more resistant to hydrolysis and thus causes the ribosome to become stopped. It is not selective for either prokaryotes or eukaryotes.
Also of note, puromycin is critical in mRNA display as it allows the growing peptide chain to be covalently bonded to its own mRNA template. Additionally, puromycin is a reversible inhibitor of dipeptidyl-peptidase II (serine peptidase) and cytosol alanyl aminopeptidase (metallopeptidase). The mechanism of inhibition is not well understood; however, puromycin can be used to distinguish between aminopeptidase M (active) and cytosol alanyl aminopeptidase (inhibited by puromycin) and therefore extremely useful in biochemistry and nephrology research.

Chemical Properties

Crystals.

Uses

Puromycin is an aminonuclease antibiotic produced by the soil actinomycete?Streptomyces alboniger; which induces apoptosis.

Uses

Puromycin has been widely used as a basic tool in research for studying protein synthesis. It is an antibiotic used by scientists in bioresearch to select cells modified by genetic engineering. It inhibits protein synthesis by binding to RNA. It is also an antineoplastic and antitrypanosomal agent.

Uses

Puromycin is a nucleoside antibiotic isolated from Streptomyces alboniger in the 1950s as an anti-trypansomal agent with antibiotic activity. Puromycin is non-selective, inhibiting RNA by blocking ribosomal translation. Puromycin is used in cell biology to select mammalian cell lines that have been transformed by vectors that express puromycin-N-acetyl-transferase.

Definition

ChEBI: An aminonucleoside antibiotic, derived from the Streptomyces alboniger bacterium, that causes premature chain termination during translation taking place in the ribosome.

Hazard

Toxic to living cells of all kinds.

Toxicity evaluation

Puromycin is a specific metabolic inhibitor of protein synthesis and acts as an aminoacyl-tRNA analog and peptidyl acceptor. The latter causes premature chain termination of the protein and the release of nascent or growing polypeptide chains. In liver, it has been shown to cause fat accumulation without causing death of the hepatocytes. Puromycin causes focal glomerular sclerosis and alters the morphology, localization of anionic sites, and metabolism of renal epithelial cells. This injury is attributable to the production of reactive oxygen species.

References

[1] ABOU-ZEID A. ABOU-ZEID  Ahmed I E D  Ahmed B Shaheen. Fermentative production of puromycin by Streptomyces alboniger[C]//23 11. 1973: 837-845. DOI: 10.1002/jctb.5020231107
[2] C RODRIGUEZ-FONSECA. Puromycin-rRNA interaction sites at the peptidyl transferase center.[J]. RNA, 2000, 6 5: 744-754. DOI: 10.1017/s1355838200000091
[3] M E AZZAM  I D A. Mechanism of puromycin action: fate of ribosomes after release of nascent protein chains from polysomes.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1973, 70 12: 3866-3869. DOI: 10.1073/pnas.70.12.3866
[4] R LÜHRMANN. Localization of the puromycin binding site on the large ribosomal subunit of Escherichia coli by immunoelectron microscopy.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1981, 78 12: 7276-7280. DOI: 10.1073/pnas.78.12.7276
[5] ROHIT SINGH  Robert V  Jessica Williams. Puromycin based inhibitors of aminopeptidases for the potential treatment of hematologic malignancies[J]. European Journal of Medicinal Chemistry, 2017, 139: Pages 325-336. DOI: 10.1016/j.ejmech.2017.07.048
[6] ROSEMARY M. EKONG . Comparison of the in vitro activities of quassinoids with activity against Plasmodium falciparum, anisomycin and some other inhibitors of eukaryotic protein synthesis[J]. Biochemical pharmacology, 1990, 40 2: Pages 297-301. DOI: 10.1016/0006-2952(90)90691-d
[7] AVINER R. The science of puromycin: From studies of ribosome function to applications in biotechnology.[J]. Computational and structural biotechnology journal, 2020: 1074-1083. DOI: 10.1016/j.csbj.2020.04.014

PUROMYCIN Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from PUROMYCIN manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
PUROMYCIN 53-79-2
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-24

53-79-2, PUROMYCINRelated Search:


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