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Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1CC(O)C(COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OC2CC(OC2CO)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)O1

InChIKey

InChIKey=IAFFAQOEDDZUHD-UHFFFAOYSA-N

Formula

C90H117N45O67P16

Mass

3396.754

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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 heteropolycyclic compounds

Substituents

(3'->5')-dinucleotide - Purine 2'-deoxyribonucleoside diphosphate - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - Organic pyrophosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Imidolactam - Alkyl phosphate - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxide - Primary alcohol - Primary amine - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic 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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