Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)NC1=NC(=O)N(C=C1)C1CC(OP(O)(=O)OCC2OC(CC2OC(C)=O)N2C=C(F)C(=O)NC2=O)C(CO)O1

InChIKey

InChIKey=BITODDDCTQEZGE-UHFFFAOYSA-N

Formula

C36H55FN5O13P

Mass

815.83

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

(3'->5')-dinucleotides and analogues

Subclass

(3'->5')-dinucleotides

Intermediate Tree Nodes

Not available

Direct Parent

(3'->5')-dinucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

(3'->5')-dinucleotide - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - N-arylamide - Halopyrimidine - Pyrimidone - Dialkyl phosphate - Aryl fluoride - Aryl halide - Fatty amide - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Fatty acyl - Tetrahydrofuran - Vinylogous amide - Heteroaromatic compound - Urea - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Lactam - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organopnictogen compound - Organohalogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organofluoride - Organonitrogen compound - Alcohol - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as (3'->5')-dinucleotides. These are dinucleotides where the two bases are connected via a (3'->5')-phosphodiester linkage.

External Descriptors

Not available

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