Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1OC(CSCCNCC2CC3=C(CN2)C=C(C=C3)[N+]([O-])=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=XTRSLZMJUJDRCM-IIGLSMPRSA-N

Formula

C22H28N8O5S

Mass

516.58

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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 - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Tetrahydroisoquinoline - Imidazopyrimidine - Purine - Nitroaromatic compound - Aminopyrimidine - Aralkylamine - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Imidazole - Oxolane - Azole - 1,2-diol - C-nitro compound - Organic nitro compound - Secondary alcohol - Secondary amine - Organic 1,3-dipolar compound - Azacycle - Thioether - Oxacycle - Sulfenyl compound - Secondary aliphatic amine - Dialkylthioether - Organoheterocyclic compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Primary amine - Alcohol - Organic zwitterion - Organic salt - Organic oxygen 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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