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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](OP(O)(=O)OC[C@H]3O[C@H]([C@H](F)[C@@H]3OP(O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=BNNGLFIWFZDMGL-ABWOQUTGSA-N

Formula

C29H37FN10O17P2

Mass

878.614

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Oligonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Oligonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

(3'->5')-oligonucleotide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine ribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Oxolane - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Urea - 1,2-diol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Alkyl halide - Organic nitrogen compound - Alcohol - Organohalogen compound - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organofluoride - Primary alcohol - Primary amine - Organonitrogen compound - Amine - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as oligonucleotides. These are organic polymers made up of a sequence of 3 to 12 purine or pyrimidine nucleotide residues linked to one another from the 5' -end to the 3'-end through a phosphate group.

External Descriptors

Not available

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