5-Methyluridine-2 13C

Product Name 5-Methyluridine-2 13C
Alternate Names Uridine Stable Isotopes, Stable Isotopes of Uridine
CAT No. CS-T-58807
CAS No. 478510-98-4
Category Stable Isotopes
Stock Enquire
Mol. Wt. 259.22 g/mol
Mol. For. C9¹³CH14N2O6
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Uridine
Smileys CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
Canonical Smiles CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
InchIKey DWRXFEITVBNRMK-FOMPHFHGSA-N
Inchl InChI=1S/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1/i7+1
IUPAC 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)(313C)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
Controlled No
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5-Methyluridine-2 13C is a chemical compound that is widely used in research and development of pharmaceuticals, nucleoside analogs, and anti-viral drugs. This molecule is a stable isotopic form of 5-Methyluridine, which is an important nucleoside component of RNA. The substitution of carbon-13 isotope in this compound helps in identifying the metabolic pathways of 5-Methyluridine and its derivatives. 5-Methyluridine-2 13C is used in various biochemical studies to trace the metabolic pathways of RNA nucleosides. It is also used in the synthesis of labeled RNA molecules for NMR and mass spectrometry analysis. Additionally, this compound is used in the development of anti-viral and anti-cancer drugs as it plays a crucial role in the inhibition of viral replication and cancer cell proliferation. From a chemical perspective, 5-Methyluridine-2 13C is a nucleoside that consists of a base, uracil and a sugar, ribose. The carbon-13 isotope is substituted at the second position of the ribose sugar, which is chemically inert and does not affect the functional properties of the molecule. The molecular formula of 5-Methyluridine-2 13C is C10H13N2O6^13C, and its molecular weight is 273.22 g/mol. In conclusion, 5-Methyluridine-2 13C is an important chemical compound used in various biochemical studies and medicinal research. Its stable isotopic substitution makes it an essential tool for tracing metabolic pathways and developing drugs for viral and cancer diseases.

Related Compounds

Uridine-[5',5'-D2] | Ara-uridine-5'-monophosphate disodium salt 13C,15N2 | Uridine 5'-Diphospho-a-D-glucose 13C6 Diammonium Salt | Uridine-3’,5’-cyclic-13C5 Monophosphate Sodium Salt | Uridine-2 13C-1,3 15N2 | Ara-uridine 13C5 | Tetrahydro uridine D3 | Uridine-5,6-d2 | Trifluridine 13C15N2 |

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