Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2CC(SC3C[C@H](O)[C@@H](CO)O3)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=BVPRLMYDUPPNET-FWRUBVDSSA-N

Formula

C15H25N2O16P3S

Mass

614.34

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine deoxyribonucleotides

Intermediate Tree Nodes

Pyrimidine deoxyribonucleoside triphosphates

Direct Parent

Pyrimidine 2',3'-dideoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside triphosphate - 2',3'-dideoxy-3'-thionucleoside triphosphate - Pentose phosphate - 2',3'-dideoxy-3'-thionucleoside - Monosaccharide phosphate - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Phosphoric acid ester - Monosaccharide - Pyrimidine - Organic phosphoric acid derivative - Alkyl phosphate - Heteroaromatic compound - Monothioacetal - Oxolane - Vinylogous amide - Secondary alcohol - Urea - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleoside triphosphates. These are pyrimidine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

Previous Back Next