Structure Information
Structure

Compound Identification

SMILES

CCC1=C(SC2=CC(C)=CC(C)=C2)N(CCCCC(=O)NCCCCCCCCCCNC(=O)CCC2=CN([C@H]3C[C@H](N=[N+]=[N-])[C@@H](CO)O3)C(=O)NC2=O)C(=O)NC1=O

InChIKey

InChIKey=VWIDTURBGDJKBB-XNPVHZECSA-N

Formula

C41H59N9O8S

Mass

838.04

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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 - Diarylthioether - Aryl thioether - M-xylene - Xylene - Thiophenol ether - Pyrimidone - Monocyclic benzene moiety - Fatty amide - Hydropyrimidine - N-acyl-amine - Benzenoid - Vinylogous thioester - Fatty acyl - Pyrimidine - Vinylogous amide - Oxolane - Heteroaromatic compound - Azo compound - Azo imide - Carboxamide group - Lactam - Secondary carboxylic acid amide - Urea - Organoheterocyclic compound - Azacycle - Sulfenyl compound - Oxacycle - Thioether - Carboxylic acid derivative - Primary alcohol - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Alcohol - Organic salt - Organic nitrogen compound - Organosulfur compound - Carbonyl group - 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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