Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OP(O)(=O)OP(O)(=O)OCC1OC(CC1N=[N+]=[N-])N1C=C(C)C(=O)NC1=O)OC(=O)CCCCCCCCCCCCCCCCC

InChIKey

InChIKey=BEQHVQYQYXNMAF-UHFFFAOYSA-N

Formula

C49H90N5O17P3

Mass

1114.198

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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 - Diacyl-glycerol-3-pyrophosphate - Glycerophospholipid - Fatty acid ester - Pyrimidone - Monoalkyl phosphate - Dicarboxylic acid or derivatives - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Fatty acyl - Heteroaromatic compound - Vinylogous amide - Oxolane - Carboxylic acid ester - Urea - Azo compound - Lactam - Azo imide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organic salt - Organic oxygen compound - Organic cation - 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

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