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6-METHYLAMINOPURINE 9-RIBOFURANOSIDE

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6-METHYLAMINOPURINE 9-RIBOFURANOSIDE Basic information

Product Name:
6-METHYLAMINOPURINE 9-RIBOFURANOSIDE
Synonyms:
  • CS-1297
  • Adenosine Impurity 15
  • NSC-29409
  • 6-Methylaminopurine D-riboside
  • 6-Methylaminopurine ribonucleoside
  • 6-Methylaminopurinosine
  • Adenosine, N-methyl-
  • (2R,3S,4R,5R)-2-(HydroxyMethyl)-5-(6-(MethylaMino)-9H-purin-9-yl)tetrahydrofuran-3,4-diol
CAS:
1867-73-8
MF:
C11H15N5O4
MW:
281.27
EINECS:
200-001-2
Product Categories:
  • Inhibitors
Mol File:
1867-73-8.mol
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6-METHYLAMINOPURINE 9-RIBOFURANOSIDE Chemical Properties

Melting point:
172 °C
Boiling point:
649.1±65.0 °C(Predicted)
Density 
1.85±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
pka
13.12±0.70(Predicted)
form 
Powder
Stability:
Hygroscopic
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6-METHYLAMINOPURINE 9-RIBOFURANOSIDE Usage And Synthesis

Description

N6-Methyladenosine is an adenosine analog. It inhibits epinephrine-induced contraction of isolated guinea pig ileum and thoracic aorta when used at a concentration of 10 μM. N6-Methyladenosine (1 mg/kg, i.v.) decreases arterial blood pressure and renal blood flow and increases peripheral resistance in anesthetized dogs. It also inhibits tumor growth in the C3H/ST and C3HB/ST mouse models of spontaneous mammary adenocarcinomas. N6-Methyladenosine is also the most prevelant mRNA modification in eukaryotes and has roles in cell viability and development.

Uses

N6-Methyladenosine is the most common internal modification of eukaryotic mRNA. The result of this modification is specifically recognized mRNA in the cytoplasm which regulates mRNA stability.N6-Methyladenosine is made when a protein complex containin the writer enzyme METTL3 adds a methyl group to adenosine. Two different eraser enzymes ALKBH5 and FTO can remove a methyl group to turn m6A bach into adenosine.

Definition

ChEBI: A methyladenosine compound with one methyl group attached to N6 of the adenine nucleobase.

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