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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O.CC(C)C1=C(SC2=CC(Cl)=CC(Cl)=C2)N(CC2=CC=NC=C2)C(COC(N)=O)=N1

InChIKey

InChIKey=GBENCFDUSWRHGI-XKPASDJRSA-N

Formula

C30H33Cl2N9O6S

Mass

718.61

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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

Not available

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside - Diarylthioether - 1,2,4,5-tetrasubstituted imidazole - Aryl thioether - 1,3-dichlorobenzene - Thiophenol ether - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - N-substituted imidazole - Pyridine - Pyrimidine - Benzenoid - Vinylogous amide - Azole - Carbamic acid ester - Imidazole - Oxolane - Heteroaromatic compound - Urea - Azo imide - Azo compound - Lactam - Thioether - Oxacycle - Sulfenyl compound - Azacycle - Organoheterocyclic compound - Primary alcohol - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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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