Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O.CCCC1=CC(=O)OC2=C1C1=C(C=CC(C)(C)O1)C1=C2[C@@H](O)[C@H](C)[C@@H](C)O1

InChIKey

InChIKey=BINWWOBGDPSSBW-GCUCKBNYSA-N

Formula

C32H39N5O9

Mass

637.69

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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

Pyranocoumarin - Angular pyranocoumarin - Pyrimidine 2',3'-dideoxyribonucleoside - Pyranochromene - 2,2-dimethyl-1-benzopyran - Coumarin - Chromane - Benzopyran - 1-benzopyran - Alkyl aryl ether - Pyrimidone - Pyranone - Pyrimidine - Hydropyrimidine - Pyran - Benzenoid - Vinylogous amide - Heteroaromatic compound - Oxolane - Azo compound - Azo imide - Lactam - Lactone - Urea - Secondary alcohol - Azacycle - Oxacycle - Ether - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic salt - Organic zwitterion - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic 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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