Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@H]1C[C@H](OP(O)(O)=O)[C@@H](COC(C[C@H]2O[C@H](C[C@@H]2OP(O)(O)=O)N2C=NC3=C2N=CN=C3N)[C@H]2O[C@H](C[C@@H]2O)N2C=NC3=C2N=CN=C3N)O1

InChIKey

InChIKey=YAKLLFOEUQFXLI-PQKNJGAISA-N

Formula

C29H37N13O14P2

Mass

853.64

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Ribonucleoside 3'-phosphates

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Ribonucleoside 3'-phosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Ribonucleoside 3'-phosphate - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Pyrimidine - Hydropyrimidine - Alkyl phosphate - N-substituted imidazole - Imidolactam - Oxolane - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Primary amine - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as ribonucleoside 3'-phosphates. These are ribonucleosides that contain a phosphate group attached to the C-3 carbon of the ribose or deoxyribose moiety. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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