Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@@H]2C[C@@H](O)[C@H](COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3COP(O)(=S)OC3C=CCOC3CO)O2)C(=O)NC1=O

InChIKey

InChIKey=VWBFACVPIBMKHZ-RQLIEXKLSA-N

Formula

C94H140N2O61P14S14

Mass

3156.58

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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

Polysaccharide - Pyrimidine 2'-deoxyribonucleoside - Pyrimidone - Thiophosphate diester - Hydropyrimidine - Thiophosphoric acid ester - Pyran - Pyrimidine - Organic thiophosphoric acid or derivatives - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Lactam - Urea - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - 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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