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SBR00017

Sigma-Aldrich

Puromycin aminonucleoside Ready Made Solution

10 mg/mL in water

Sinonimo/i:

3′-Amino-3′-deoxy-N6,N6-dimethyladenosine

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1 ML
CHF 157.00

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1 ML
CHF 157.00

About This Item

Formula empirica (notazione di Hill):
C12H18N6O3
Numero CAS:
Peso molecolare:
294.31
Codice UNSPSC:
51281912
NACRES:
NA.85

CHF 157.00


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Saggio

≥98%

Livello qualitativo

Stato

liquid

Concentrazione

10 mg/mL in water

Spettro attività antibiotica

Gram-positive bacteria
neoplastics
parasites

Modalità d’azione

protein synthesis | interferes

Temperatura di conservazione

2-8°C

Stringa SMILE

N[C@H]1[C@@H](O)[C@H](N(C=N2)C3=C2C(N(C)C)=NC=N3)O[C@@H]1CO

InChI

1S/C12H18N6O3/c1-17(2)10-8-11(15-4-14-10)18(5-16-8)12-9(20)7(13)6(3-19)21-12/h4-7,9,12,19-20H,3,13H2,1-2H3
RYSMHWILUNYBFW-UHFFFAOYSA-N

Azioni biochim/fisiol

Puromycin aminonucleoside is an aminonucleoside derivative of the known antibiotic puromycin. Puromycin aminonucleoside has been used in nephrology research, studying focal and segmental glomerulosclerosis, and in the induction of nephrosis in rats.[1][2][3] Rats with puromycin aminonucleoside-induced nephrotic syndrome were used to study the excretion of sodium and NOx metabolites.[4]

Puromycin aminonucleoside has also been used to probe endothelial glycosaminoglycan synthesis in cultured glomerular endothelial cells and their relation to cell permeability.[5] A puromycin aminonucleoside nephrosis model of rat glomerular disease was also used to study the role of the neuron-specific ubiquitin C-terminal hydrolase protein gene product 9.5 (PGP 9.5).[6]

Nota sulla preparazione

Puromycin aminonucleoside solution is provided at 10 mg/mL in water and could be further diluted in aqueous buffers to a working concentration of 10 μg/mL (1:1000).

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Jenny Sörensson et al.
American journal of physiology. Renal physiology, 284(2), F373-F380 (2002-10-22)
It has been suggested that proteinuria is caused by alterations of the charge selectivity of the basement membrane and/or the epithelial cell layer (podocytes). However, recent findings suggest that the endothelial luminal surface coat, consisting of proteoglycans with their connected
Alicia A McDonough et al.
Current opinion in nephrology and hypertension, 12(5), 533-541 (2003-08-16)
The proximal tubule sodium/hydrogen exchanger continuously reabsorbs the bulk of the filtered sodium, controlling salt delivery to the distal nephron which is critical for tubuloglomerular feedback autoregulation and for fine control of salt excretion in the distal nephron. This review
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Agnes B Fogo
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Glomerulosclerosis in a heterogeneous pattern, ie, focal and segmental glomerulosclerosis (FSGS), is a common endpoint in a variety of settings, including idiopathic FSGS, and scarring secondary to other renal or systemic diseases. These different causes contribute to the diverse clinical
Zhenmin Ni et al.
Biochimica et biophysica acta, 1638(2), 129-137 (2003-07-11)
Blood pressure is frequently elevated, blood volume is usually normal or increased and plasma renin and aldosterone are usually low in nephrotic syndrome (NS). These observations challenge the conventional view attributing sodium retention in NS to a hypoalbuminemia-induced intravascular volume

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