Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N([C@H]1C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1)C(SCCS(=O)(=O)CCCCCCS(=O)(=O)CCSC1=NC3=C(N=CN=C3N)N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O)=N2

InChIKey

InChIKey=LJTVLJCFFHHENL-DJJZFNOQSA-N

Formula

C30H50N10O30P6S4

Mass

1344.85

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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 triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Purine 2'-deoxyribonucleoside triphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aryl thioether - Aminopyrimidine - Monoalkyl phosphate - Alkylarylthioether - Pyrimidone - N-substituted imidazole - Monosaccharide - Pyrimidine - Organic phosphoric acid derivative - Imidolactam - Alkyl phosphate - Phosphoric acid ester - Sulfonyl - Sulfone - Heteroaromatic compound - Azole - Imidazole - Vinylogous amide - Oxolane - Secondary alcohol - 1,2-diol - Sulfenyl compound - Thioether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Organosulfur compound - Primary amine - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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