Pyrimidine ribonucleoside monophosphates
Pyrimidine Ribonucleoside Monophosphates are a class of nucleotides derived from pyrimidines, which play crucial roles in cellular metabolism and genetic information transfer. These compounds consist of a pyrimidine ring (either cytidine or uridine) linked to a ribose sugar through a glycosidic bond, and further esterified at the 5' position with a phosphate group. They are essential intermediates in nucleotide biosynthesis pathways, particularly in DNA replication and RNA synthesis.
In biological systems, pyrimidine ribonucleoside monophosphates serve as precursors for further phosphorylation to diphosphate (DP) and triphosphate (TP) forms. The TP form is a key component of ATP analogs used in various research applications such as in vitro transcription, reverse transcriptase assays, and mutagenesis studies.
These compounds are widely utilized in the pharmaceutical industry for drug development, gene therapy, and diagnostic tools. Their stability and reactivity make them valuable reagents in synthetic biology, molecular cloning, and other advanced biochemical techniques.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Cytidine 5'-monophosphate | 63-37-6 | C9H14N3O8P |
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[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid | 28086-43-3 | C9H13N2O9P |
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5690-54-0 | C9H11N2O9P | |
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Agrocin 108 | 101026-84-0 | C20H29N4O16P |
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5-Methylcytidine-5'-monophosphate | 3590-36-1 | C10H16N3O8P |
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5'-Cytidylic acid, 5-bromo- | 4181-56-0 | C9H13BrN3O8P |
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2(1H)-Pyrimidinone,4-amino-1-[5-O-[hydroxy(octadecyloxy)phosphinyl]-b-D-arabinofuranosyl]-, sodium salt (1:1) | 65093-40-5 | C27H50N3NaO8P |
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Barium(2+);[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-imino-2-oxidopyrimidin-1-yl)oxolan-2-yl]methyl hydrogen phosphate | 13435-44-4 | C9H12BaN3O8P |
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Uridine 5′-monophosphate disodium salt | 3387-36-8 | C9H11N2Na2O9P |
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cytidylyl(5'→2')adenosine | 10318-62-4 | C19H25N8O11P |
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