Structure Information
Structure

Compound Identification

SMILES

CC1=C(CCOP(O)(=O)OP(O)(=O)OC[C@@H]2O[C@H]([C@H](O)[C@H]2O)N2C=NC3=C2N=CN=C3N)SC(=N1)C(O)=O

InChIKey

InChIKey=VGXBGQACJQRWLV-LQZWOCCTSA-N

Formula

C17H22N6O12P2S

Mass

596.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside diphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - 6-aminopurine - Pentose monosaccharide - Organic pyrophosphate - Imidazopyrimidine - Purine - 2,4,5-trisubstituted 1,3-thiazole - Thiazolecarboxylic acid or derivatives - Monoalkyl phosphate - Aminopyrimidine - N-substituted imidazole - Alkyl phosphate - Imidolactam - Monosaccharide - Phosphoric acid ester - Pyrimidine - Organic phosphoric acid derivative - Heteroaromatic compound - Thiazole - Azole - Imidazole - Oxolane - Amino acid or derivatives - Secondary alcohol - Amino acid - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Alcohol - Primary amine - Organic oxide - Hydrocarbon derivative - Amine - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside diphosphates. These are purine ribobucleotides with diphosphate group linked to the ribose moiety.

External Descriptors

Not available

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