Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(=O)O[C@@H]2[C@@H](CO[P+](O)=O)O[C@H]([C@@H]2O)N2C=CC(=O)NC2=O)[C@@H](OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(N)=NC2=O)N2C=CC(=O)NC2=O)[C@H]1O

InChIKey

InChIKey=HJXREQCPAINLRE-ZKVOPUEUSA-O

Formula

C37H47N12O30P4

Mass

1263.731

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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

Purine ribonucleoside bisphosphates

Direct Parent

Purine ribonucleoside 3',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside 3',5'-bisphosphate - Pyrimidine ribonucleoside 3',5'-bisphosphate - Pyrimidine ribonucleoside bisphosphate - Pyrimidine ribonucleoside monophosphate - Purine ribonucleoside phosphonate - Ribonucleoside 3'-phosphate - Pentose phosphate - Pentose-5-phosphate - Deoxyribo- or ribonucleoside phosphonate - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Pyrimidone - Dialkyl phosphate - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Organic phosphoric acid derivative - Alkyl phosphate - Hydropyrimidine - Phosphoric acid ester - Heteroaromatic compound - Vinylogous amide - Oxolane - Imidazole - Azole - 1,2-diol - Secondary alcohol - Urea - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Primary amine - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside 3',5'-bisphosphates. These are purine ribobucleotides with one phosphate group attached to 3' and 5' hydroxyl groups of the ribose moiety.

External Descriptors

Not available

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