Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OCCC(=O)NCCCCCCNC(=O)CC2=CN([C@H]3C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O3)C(=O)NC2=O)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=NAZWDAALCUAHFM-PZBRJEMOSA-N

Formula

C26H45N4O22P3

Mass

858.573

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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'-deoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside triphosphate - Pentose phosphate - Glycosyl compound - O-glycosyl compound - Monosaccharide phosphate - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Monosaccharide - Alkyl phosphate - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Oxolane - Carboxamide group - Lactam - Urea - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Polyol - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organic oxide - Organooxygen compound - Carbonyl group - Primary alcohol - Aromatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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