Purine deoxyribonucleoside monophosphates
Purine Deoxyribonucleoside Monophosphates (dCMP, dAMP, and dGMP) are essential components in the biosynthesis of DNA. They serve as immediate precursors for nucleotide synthesis pathways within cells. These compounds are derived from purine bases and ribose-5-phosphate through a series of enzymatic reactions. In molecular biology research, these monophosphates play crucial roles in studying gene expression, cell proliferation, and DNA repair mechanisms. Additionally, they are utilized in the development of nucleoside analogs for therapeutic applications, including anti-viral and anti-cancer treatments. Understanding their biochemical properties is vital for researchers focusing on genetic analysis and molecular biology.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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POLYDEOXYADENYLIC ACID-POLYTHYMIDYLIC ACID SODIUM SALT | 86834-22-2 | C20H29N7O14P2 |
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2'-Deoxyinosine 5'-Monophosphate Disodium Salt | 14999-52-1 | C10H11N4Na2O7P |
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5'-Adenylic acid,3'-amino-3'-deoxy-N,N-dimethyl- (9CI) | 26113-03-1 | C12H19N6O6P |
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Adenosine, 2'-deoxy-,5'-(trihydrogen imidodiphosphate) (9CI) | 119447-19-7 | C10H16N6O8P2 |
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5'-Guanylic acid,2'-deoxy-7,8-dihydro-8-oxo- | 127027-50-3 | C10H14N5O8P |
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6-Mehylaminopurindeoxyribosid-5'-monophosphat | 53696-69-8 | C11H16N5O6P |
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9-(2-Chloro-2-deoxy-5-O-phosphono-β-D-arabinofuranosyl)-2-fluoro-9H-purin-6-amine | 548774-56-7 | C10H12ClFN5O6P |
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2'-Deoxyguanine monophosphate | 7720-24-3 | C10H12N5O7P |
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poly(2'-fluoro-2'-deoxyadenylic acid) | 68245-92-1 | C10H13FN5O6P |
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5'-Guanylic acid, 2'-deoxy-2'-fluoro- | 170784-58-4 | C10H13FN5O7P |
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