Puromycin aminonucleoside

Synonyms: NSC 3056, PAN, Stylomycin aminonucleoside, ARDMA, SAN

Puromycin aminonucleoside (NSC 3056, PAN, Stylomycin aminonucleoside, ARDMA, SAN), the aminonucleoside portion of the antibiotic puromycin, is a reversible inhibitor of dipeptidyl-peptidase II and cytosol alanyl aminopeptidase that induces apoptosis in mesangial cells (MCs) accompanied by declined cell viability and enhanced inflammatory response.

Puromycin aminonucleoside Chemical Structure

Puromycin aminonucleoside Chemical Structure

CAS: 58-60-6

Selleck's Puromycin aminonucleoside has been cited by 3 publications

Purity & Quality Control

Batch: S963101 DMSO] 59 mg/mL] false] Water] 30 mg/mL] false] Ethanol] Insoluble] false Purity: 99.91%
99.91

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Biological Activity

Description Puromycin aminonucleoside (NSC 3056, PAN, Stylomycin aminonucleoside, ARDMA, SAN), the aminonucleoside portion of the antibiotic puromycin, is a reversible inhibitor of dipeptidyl-peptidase II and cytosol alanyl aminopeptidase that induces apoptosis in mesangial cells (MCs) accompanied by declined cell viability and enhanced inflammatory response.
Targets
DPP-2 [1] cytosol alanyl aminopeptidase [1]
In vitro
In vitro

Puromycin aminonucleoside (PAN) induces MC apoptosis accompanied by the declined cell viability and enhanced inflammatory response. In PAN-treated MCs, ERRα overexpression further aggravates PAN-induced apoptosis.[1]

Cell Research Cell lines mouse mesangial cells
Concentrations 50 μg/ml, 100 μg/ml
Incubation Time 24 h
Method

For apoptosis assay, mesangial cells are treated with PAN for 24 h at the indicated concentration. After treatment, cells are stained with FITC-Annexin V and PI according to the manufacturer’s protocol. Cell apoptosis is determined using a BD FACS Calibur flow cytometer and data is analyzed with Flowjo software.

In Vivo
In vivo

In agreement with the in vitro study, increased ERRα expression is observed in line with enhanced apoptotic response in renal cortex from PAN-treated rats.[1]

Animal Research Animal Models male Sprague-Dawley rats
Dosages 150 mg/kg
Administration IV

Chemical lnformation & Solubility

Molecular Weight 294.31 Formula

C12H18N6O3

CAS No. 58-60-6 SDF --
Smiles CN(C)C1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)N)O
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 59 mg/mL ( (200.46 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 30 mg/mL

Ethanol : Insoluble


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In vivo
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Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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