CAS 5746-29-2

6-methoxy-9-pentofuranosyl-9H-purine

Description:

6-Methoxy-9-pentofuranosyl-9H-purine, with the CAS number 5746-29-2, is a purine nucleoside derivative characterized by its structural components, which include a purine base and a sugar moiety. This compound features a methoxy group at the 6-position of the purine ring and a pentofuranosyl sugar, which is a five-membered sugar ring. The presence of the methoxy group can influence the compound's solubility, stability, and biological activity. As a nucleoside, it plays a role in various biochemical processes, including nucleic acid synthesis and cellular signaling. The compound may exhibit properties relevant to medicinal chemistry, particularly in the context of antiviral or anticancer research, due to its structural similarity to naturally occurring nucleosides. Its specific interactions and mechanisms of action would depend on its ability to be incorporated into nucleic acids or to interact with enzymes involved in nucleic acid metabolism. Further studies would be necessary to elucidate its full biological profile and potential applications.

Formula: C₁₁H₁₄N₄O₅

InChI: InChI=1/C11H14N4O5/c1-19-10-6-9(12-3-13-10)15(4-14-6)11-8(18)7(17)5(2-16)20-11/h3-5,7-8,11,16-18H,2H2,1H3

SMILES: COc1c2c(ncn1)n(cn2)C1C(C(C(CO)O1)O)O

Synonyms:

• 9H-purine, 6-methoxy-9-pentofuranosyl-

6-METHOXYPURINE RIBOSIDE

CAS: 5746-29-2

Formula: C₁₁H₁₄N₄O₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 282.2527

Ref: IN-DA00EKSA

6-O-Methylinosine

CAS: 5746-29-2

6-O-Methylinosine

Purity: 97%

Molecular weight: 282.25g/mol

Ref: 54-OR1012037

6-O-Methylinosine

CAS: 5746-29-2

6-O-Methylinosine is a Nucleoside Derivative - 6-Modified purine nucleoside.

Formula: C₁₁H₁₄N₄O₅

Color and Shape: Solid

Molecular weight: 282.25

Ref: TM-TNU0155

6-O-Methylinosine

CAS: 5746-29-2

6-O-Methylinosine is a modified nucleoside that is used in the synthesis of recombinant proteins. It is synthesized from the reaction of methylphosphate and 6-O-methylguanosine. The phosphate group of the 6-O-methylguanosine molecule reacts with methylphosphate in an acid or neutral environment, while it reacts with phosphoric acid in a basic environment. This reaction can be monitored by measuring the amount of free phosphate groups present after the reaction. The rate of this reaction can be increased by increasing temperature and pH. 6-O-Methylinosine has been shown to have anticancer activity, which may be due to its ability to inhibit enzyme catalysis and modify DNA structure.

Formula: C₁₁H₁₄N₄O₅

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 282.25 g/mol

Ref: 3D-NM144751