CCCCCC\C=[N+](\[O-])CC1OC(C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)N1C=CC(=O)NC1=O

InChIKey=SYXSWHKGKRVSGC-UXHLAJHPSA-N

C28H53N3O6Si2

583.917

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

Glycosylamines Pyrimidones Hydropyrimidines Monosaccharides Vinylogous amides Trialkylheterosilanes Heteroaromatic compounds Oxolanes Ureas Silyl ethers Shiff bases Lactams Nitrones Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Organic metalloid salts Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organic zwitterions Organopnictogen compounds

Aromatic heteromonocyclic compounds

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Trialkylheterosilane - Heteroaromatic compound - Oxolane - Vinylogous amide - Lactam - Nitrone - Shiff base - Urea - Silyl ether - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic salt - Organosilicon compound - Organic oxide - Organic zwitterion - Hydrocarbon derivative - Organic metalloid moeity - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

Not available