ChemicalBook--->CAS DataBase List--->1867-73-8

1867-73-8

1867-73-8 Structure

1867-73-8 Structure
IdentificationBack Directory
[Name]

6-METHYLAMINOPURINE 9-RIBOFURANOSIDE
[CAS]

1867-73-8
[Synonyms]

CS-1297
N6-Me-A
N6-Me-rA
NSC-29409
N-Methyladenosine
Adenosine, N-methyl-
Adenosine Impurity 15
6-Methylaminopurinosine
N6-methyladenosine (m6A)
6-Methylaminopurine D-riboside
6-Methylaminopurine ribonucleoside
6-METHYLAMINOPURINE 9-RIBOFURANOSIDE
(2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-methylaminopurin-9-yl)oxolane-3,4-diol
(2R,3S,4R,5R)-2-(HydroxyMethyl)-5-(6-(MethylaMino)-9H-purin-9-yl)tetrahydrofuran-3,4-diol
[EINECS(EC#)]

200-001-2
[Molecular Formula]

C11H15N5O4
[MDL Number]

MFCD00005739
[MOL File]

1867-73-8.mol
[Molecular Weight]

281.27
Chemical PropertiesBack Directory
[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)
[form ]

Powder
[pka]

13.12±0.70(Predicted)
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

6-METHYLAMINOPURINE 9-RIBOFURANOSIDE(1867-73-8)MS
6-METHYLAMINOPURINE 9-RIBOFURANOSIDE(1867-73-8)IR1
6-METHYLAMINOPURINE 9-RIBOFURANOSIDE(1867-73-8)IR2
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