CAS 35542-01-9: 5-Methoxyuridine
Formula:C10H14N2O7
InChI:InChI=1S/C10H14N2O7/c1-18-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)19-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1
InChI key:InChIKey=ZXIATBNUWJBBGT-JXOAFFINSA-N
SMILES:O[C@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C=C(OC)C(=O)NC2=O
Synonyms:- Uridine, 5-methoxy-
- 5-Methoxyuridine
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Found 7 products.
5-Methoxyuridine
CAS:5-Methoxyuridine is a nucleoside that is structurally related to uridine. It is an intermediate in the biosynthesis of pyrimidines and is also used as a precursor for other compounds. 5-Methoxyuridine has been shown to inhibit protein synthesis by binding to purine receptors and inhibiting the function of protein kinases. The x-ray crystal structures of 5-methoxyuridine bound to two different p2y receptors have been determined. The analytical chemistry of 5-methoxyuridine is based on UV absorption measurements, which are able to identify hydrogen bonds between the base and the sugar moiety. This drug has been investigated for its potential use in cancer therapy due to its ability to inhibit RNA synthesis, which can lead to cell death by incomplete replication or transcription. 5-Methoxyuridine inhibits messenger RNA (mRNA) production in bacteria by interfering with sequence recognition and binding sites within the ribosome and preventingFormula:C10H14N2O7Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:274.23 g/mol5-Methoxyuridine
CAS:5-Methoxyuridine (Mo5U) is an antitumor purine analog that inhibits DNA synthesis and induces apoptosis in lymphatic cancers.Formula:C10H14N2O7Purity:99.43%Color and Shape:SolidMolecular weight:274.235-Methoxyuridine
CAS:Formula:C10H14N2O7Purity:(HPLC) ≥ 98.0%Color and Shape:White to off-white powderMolecular weight:274.231-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methoxypyrimidine-2,4(1H,3H)-dione
CAS:Purity:95.0%Molecular weight:274.22900390625
