Structure Information
Structure

Compound Identification

SMILES

CC1=NC2=C(N=CN2[C@H]2O[C@H](CS)[C@@H](OP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@H]2O)C(N)=N1

InChIKey

InChIKey=IKGRYALWOXQHIM-FCKMSMMTSA-N

Formula

C11H18N5O12P3S

Mass

537.27

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

5'-deoxy-5'-thionucleosides

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxy-5'-thionucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxy-5'-thionucleoside - Ribonucleoside 3'-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyrimidine - Alkyl phosphate - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Azacycle - Organoheterocyclic compound - Alkylthiol - Oxacycle - Organosulfur compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Amine - Primary amine - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxy-5'-thionucleosides. These are 5'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.

External Descriptors

Not available

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