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SBR00017

Sigma-Aldrich

Puromycin aminonucleoside Ready Made Solution

10 mg/mL in water

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C12H18N6O3
Número CAS:
Peso molecular:
294.31
Código UNSPSC:
51281912
NACRES:
NA.85

Ensaio

≥98%

Nível de qualidade

forma

liquid

concentração

10 mg/mL in water

espectro de atividade do antibiótico

Gram-positive bacteria
neoplastics
parasites

Modo de ação

protein synthesis | interferes

temperatura de armazenamento

2-8°C

cadeia de caracteres 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

chave InChI

RYSMHWILUNYBFW-UHFFFAOYSA-N

Ações bioquímicas/fisiológicas

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).

Nota de preparo

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).

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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