Structure Information
Structure

Compound Identification

SMILES

CC1=C(CCOP(=O)(OC[C@H]2O[C@H](C(O)C2O)N2C=NC3=C2N=CN=C3N)OP([O-])([O-])=O)SC=[N+]1CC1=CN=C(C)N=C1N

InChIKey

InChIKey=GBJLOHNSEPXOLB-XVCYLCILSA-M

Formula

C22H28N9O10P2S

Mass

672.53

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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 - Thiamine-phosphate - Thiamine - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - 4,5-disubstituted 1,3-thiazole - Aminopyrimidine - Dialkyl phosphate - Pyrimidine - Alkyl phosphate - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Thiazole - Azole - Imidazole - Heteroaromatic compound - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Primary amine - Organic salt - Hydrocarbon derivative - Alcohol - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic cation - 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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