Structure Information
Structure

Compound Identification

SMILES

O=C1NC(=S)NC=C1.OC[C@H]1O[C@H](C[C@@H]1O)N1C=C([Hg+])C(=O)NC1=O

InChIKey

InChIKey=JSCPLOFWXNUFFY-CDNBRZBRSA-N

Formula

C13H15HgN4O6S

Mass

555.93

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2'-deoxyribonucleosides

Alternative Parents

2-Thiopyrimidines Pyrimidinethiones Pyrimidones Aryl mercury compounds Hydropyrimidines Metal aryls Oxolanes Vinylogous amides Heteroaromatic compounds Lactams Ureas Thioureas Secondary alcohols Oxacyclic compounds Organic transition metal salts Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Organic cations

Molecular Framework

Not available

Substituents

Pyrimidine 2'-deoxyribonucleoside - 2-thiopyrimidine - Thiopyrimidine - Pyrimidinethione - Pyrimidone - Hydropyrimidine - Metal aryl - Pyrimidine - Aryl mercury compound - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Thiourea - Urea - Oxacycle - Azacycle - Organic transition metal salt - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organometallic compound - Organomercurial-compound - Organic transition metal moeity - Organic nitrogen compound - Organic oxygen compound - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

Previous Back Next