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Merck

SBR00017

Sigma-Aldrich

Puromycin aminonucleoside Ready Made Solution

10 mg/mL in water

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C12H18N6O3
Numer CAS:
Masa cząsteczkowa:
294.31
Kod UNSPSC:
51281912
NACRES:
NA.85

Próba

≥98%

Poziom jakości

Postać

liquid

stężenie

10 mg/mL in water

spektrum działania antybiotyku

Gram-positive bacteria
neoplastics
parasites

Tryb działania

protein synthesis | interferes

temp. przechowywania

2-8°C

ciąg SMILES

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

Klucz InChI

RYSMHWILUNYBFW-UHFFFAOYSA-N

Działania biochem./fizjol.

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. Rats with puromycin aminonucleoside-induced nephrotic syndrome were used to study the excretion of sodium and NOx metabolites.

Puromycin aminonucleoside has also been used to probe endothelial glycosaminoglycan synthesis in cultured glomerular endothelial cells and their relation to cell permeability. 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).

Uwaga dotycząca przygotowania

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).
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Kod klasy składowania

10 - Combustible liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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