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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](SSC3=C(C=C(C=C3)[N+]([O-])=O)[N+]([O-])=O)[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=ZMMIKAJWAPKPHV-KWCYVHTRSA-N

Formula

C16H16N4O8S2

Mass

456.44

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2',3'-dideoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2',3'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside - 2',3'-dideoxy-3'-thionucleoside - Nitrobenzene - Nitroaromatic compound - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Benzenoid - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Organic nitro compound - Organic disulfide - C-nitro compound - Urea - Lactam - Oxacycle - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Organic salt - Organic oxide - Hydrocarbon derivative - Alcohol - Organic zwitterion - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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