PUROMYCIN AMINONUCLEOSIDE

PUROMYCIN AMINONUCLEOSIDE Basic information
Product Name:PUROMYCIN AMINONUCLEOSIDE
Synonyms:3’-amino-3’-deoxy-n,n-dimethyl-adenosin;6-(dimethylamino)-9-(3-amino-3-deoxy-beta-d-ribofuranosyl)purine;9-(3-amino-3-deoxy-beta-d-ribofuranosyl)-6-(dimethylamino)-9h-purine;aminonucleoside;aminonucleosidepuromycin;stylomycinaminonucleoside;PUROMYCIN AMINONUCLEOSIDE;6-DIMETHYLAMIN-9-[3'-AMINO-3'DEOXYRIBOSYL]-PURINE
CAS:58-60-6
MF:C12H18N6O3
MW:294.31
EINECS:200-388-3
Product Categories:
Mol File:58-60-6.mol
PUROMYCIN AMINONUCLEOSIDE Structure
PUROMYCIN AMINONUCLEOSIDE Chemical Properties
Melting point 235℃ (Decomposition)
Boiling point 436.08°C (rough estimate)
density 1.2131 (rough estimate)
refractive index 1.7000 (estimate)
Fp >110°(230°F)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility H2O: 50 mg/mL, clear, slightly yellow
form liquid
pka13.26±0.70(Predicted)
color White
Water Solubility Soluble in water at 50mg/ml. May require heating
BRN 93902
Stability:Stable for 1 year as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 2 months.
InChIKeyRYSMHWILUNYBFW-GRIPGOBMSA-N
EPA Substance Registry SystemAdenosine, 3'-amino-3'-deoxy-N,N-dimethyl- (58-60-6)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 48/22
WGK Germany 3
RTECS AU7337000
10-21
TSCA Yes
HS Code 29419090
MSDS Information
ProviderLanguage
SigmaAldrich English
PUROMYCIN AMINONUCLEOSIDE Usage And Synthesis
DescriptionPuromycin aminonucleoside (58-60-6) is the nucleoside moiety of puromycin (Cat.# 10-2100) which does not inhibit protein synthesis or induce apoptosis.1?It acts as a glomerular epithelial cell toxin2 and as such is a useful tool for producing animal models of nephropathy3,4, or puromycin aminonucleoside nephrosis (1-2.5 mg/100g rat body weight)5. Active in vivo.
Chemical PropertiesWhite crystal
UsesPuromycin aminonucleoside is a semi-synthetic derivative of puromycin which lacks the methoxyphenylalanyl moiety. Puromycin aminonucleoside is the key intermediate in the synthesis of semi-synthetic analogues of puromycin. It does not inhibit protein synthesis or induce apoptosis, but exhibits antitumour properties. Puromycin aminonucleoside-induced nephrosis is a well-described model of human idiopathic nephrotic syndrome, suppressing integrin expression in cultured glomerular epithelial cells.
UsesPuromycin Aminonucleoside is an aminonucleoside portion of the antibiotic puromycin.
DefinitionChEBI: Puromycin derivative that lacks the methoxyphenylalanyl group on the amine of the sugar ring.
Safety ProfileAn experimental teratogen. Other experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.
References1) Chow et al. (1995), Reevaluation of the role of de novo protein synthesis in rat thymocyte apoptosis; Exp. Cell Res., 216 149 2) Krishnamurti et al. (2001), Puromycin aminonucleoside suppresses integrin expression in cultured glomerular epithelial cells; J. Am. Soc. Nephrol., 12 758 3) Egashira et al. (2006), Tryptophan-niacin metabolism in rat with puromycin aminonucleoside-induced nephrosis; Int. J. Vitam. Nutr. Res., 76 28 4) Hagiwara et al. (2006), Mitochondrial dysfunction in focal segmental glomerulosclerosis of puromycin aminonucleoside nephrosis; Kidney Int., 69 1146 5) Lowenborg et al. (2000), Glomerular function and morphology in puromycin aminonucleoside nephropathy in rats; Nephrol. Dial. Transplant, 15 1547
PUROMYCIN AMINONUCLEOSIDE Preparation Products And Raw materials
Raw materials3'-Azido-3'-deoxy-N6,N6-dimethyladenosine
Methylisothiazolinone Isopropyl palmitate Imidazolidinyl urea Octyl 4-methoxycinnamate Xanthan gum Butylparaben Cetearyl alcohol 4'-Hydroxyacetophenone Decanoyl/octanoyl-glycerides Triethanolamine PUROMYCIN DIHYDROCHLORIDE N6,N6-DIMETHYLADENOSINE PUROMYCIN DIHYDROCHLORIDE PUROMYCIN AMINONUCLEOSIDE PUROMYCIN DIHYDROCHLORIDE DIHYDRATE PUROMYCIN A 201A PUROMYCIN DIHYDROCHLORIDE, [8-3H(N)]-

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