Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=S)(O[C@H]3C[C@@H](O[C@@H]3CO)N3C=C(C)C(=O)NC3=O)SCCSC(=O)C3=CC=CC=C3)O2)C(=O)NC1=O

InChIKey

InChIKey=IOPGCCJOYUXVAV-CMVLJIPBSA-N

Formula

C29H35N4O11PS3

Mass

742.77

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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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside - Benzoic acid or derivatives - Thiobenzoic acid or derivatives - Benzoyl - Pyrimidone - Monocyclic benzene moiety - Dithiophosphate o-ester - Pyrimidine - Dithiophosphate s-ester - Benzenoid - Hydropyrimidine - Organic dithiophosphate - Vinylogous amide - Oxolane - Heteroaromatic compound - Secondary alcohol - Urea - Carbothioic s-ester - Thiocarboxylic acid ester - Lactam - Carboxylic acid derivative - Oxacycle - Organothiophosphorus compound - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thiocarboxylic acid or derivatives - Organooxygen compound - Organonitrogen compound - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Organic oxide - Alcohol - Hydrocarbon derivative - 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

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