CAS 55486-09-4: 5-Methyl-2′-O-methyluridine
Formula:C11H16N2O6
InChI:InChI=1S/C11H16N2O6/c1-5-3-13(11(17)12-9(5)16)10-8(18-2)7(15)6(4-14)19-10/h3,6-8,10,14-15H,4H2,1-2H3,(H,12,16,17)/t6-,7-,8-,10-/m1/s1
InChI key:InChIKey=YHRRPHCORALGKQ-FDDDBJFASA-N
SMILES:O(C)[C@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C(=O)NC(=O)C(C)=C2
Synonyms:- 1-[(2R,3R,4R,5R)-4-Hydroxy-5-(hydroxymethyl)-3-methoxytetrahydro-2-furanyl]-5-methyl-2,4(1H,3H)-pyrimidinedione
- 2'-O-Methyl-5-methyl-D-uridine
- 2′-O-Methylribothymidine
- 5,2'-O-Dimethyluridine
- 5-Methyl-2'-O-methyluridine
- uridine, 5-methyl-2'-O-methyl-
- 2′-O-Methylthymidine
- 2′-O-Methyl-5-methyluridine
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Found 6 products.
2'-O-Methyl-5-methyluridine
CAS:2'-O-Methyl-5-methyluridine is a nucleoside that is involved in the synthesis of RNA. It is a component of the 5-methyluridine (5MU) and 2'-O-methyl-5-hydroxymethyluridine (2'OMMU) families of nucleotides. This compound has been shown to be effective against organisms such as E. coli, S. typhimurium, and C. parapsilosis, which are amide sensitive. The amide group of 2'-O-methyl-5-methyluridine can be cleaved by reagents such as hydrazine or tris(2,4,6,-trimethlyphenyl)phosphonium bromide to form 5MU and 2'OMMU respectively. The modifications to the ribose ring are important for its activity and function in cells. The modification of the ribose ring is catalyzed by enzymes calledFormula:C11H16N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:272.25 g/mol5-Methyl-2'-O-methyluridine
CAS:Formula:C11H16N2O6Purity:97%Color and Shape:SolidMolecular weight:272.25452'-O-Methyl-5-methyl uridine
CAS:2'-O-Methyl-5-methyl uridine is a 2'-O-Methyl nucleoside.Formula:C11H16N2O6Color and Shape:SolidMolecular weight:272.25Ref: TM-TNU0716
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquire5-Methyl-2’-O-methyluridine
CAS:Controlled ProductApplications 5-Methyl-2’-O-methyluridine is one of three oligonucleotide in platinum-derivatized homopyrimidine triplex-forming oligonucleotides (Pt-TFOs) useful in crosslinking to the transcribed strand in the human androgen receptor (AR) gene. Inhibitory activity against M. bovis and M. avium. References Graham, M. K., et al.: Biochem., 54, 2270-2282 (2015); Johar, M., et al.: Bioorg. Med. Chem., 13, 6663-6671 (2005)Formula:C11H16N2O6Color and Shape:NeatMolecular weight:272.25
