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5-Methylcyclocytidine hydrochloride Chemical Structure 5-Methylcyclocytidine hydrochloride

Catalog NO.: NS-007 | CAS NO.: 51391-96-9 | Brand: BIOCAXIS

Category

Nucleosides & Nucleotides, nucleobase

Synonyms:

O-2,3'-Anhydro-5-methylcytidine hydrochloride; 6H-Furo[2',3':4,5]oxazolo[3,2-a]pyrimidine-2-methanol, 2,3,3a,9a-tetrahydro-3-hydroxy-6-imino-7-methyl-, monohydrochloride, [2R-(2α,3β,3aβ,9aβ)]-; (2R,3R,3aS,9aR)-2-(Hydroxymethyl)-6-imino-7-methyl-3,3a,6,9a-tetrahydro-2H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-3-ol Hydrochloride; CMC.HCl

 

Molecular Formula

C10H14ClN3O4

Molecular Weight

 275.69

General description

5-Methylcyclocytidine hydrochlorine, a nucleoside analogue of cytidine, exhibits profound biomedical implications in combating specific ailments. Its inherent capability to impede nucleotide synthesis and viral replication positions it as a prospective anticancer and antiviral agent. However, elucidating its complete therapeutic prowess necessitates further comprehensive investigation, thus underscoring the importance of conducting extensive scientific research.

5-Methylcyclocytidine hydrochloride is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.

 

 

 

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