Structure Information
Structure

Compound Identification

SMILES

[H]C1(O)CC([H])(OC1([H])COP(O)(=O)OC1([H])CC([H])(OC1([H])COP(O)(O)=O)N1C=NC2=C1NC(=N)N=C2O)N1C=C(C)C(=N)N=C1O

InChIKey

InChIKey=JAPHKTOVZDCDRM-UHFFFAOYSA-N

Formula

C20H28N8O13P2

Mass

650.435

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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 deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Purine - Imidazopyrimidine - Hydroxypyrimidine - Monoalkyl phosphate - Dialkyl phosphate - Hydropyrimidine - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - 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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