Structure Information
Structure

Compound Identification

SMILES

O[C@H]1C[C@@H](O[C@@H]1COP(O)(=O)OP(O)(=O)OP(O)(O)=O)N1C=C(\C=C\CNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)C(=O)NC1=O

InChIKey

InChIKey=IYKNGWWPNRDDHK-LKWQFPJRSA-N

Formula

C22H34N5O16P3S

Mass

749.51

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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 heteropolycyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside triphosphate - Biotin_derivative - Thienoimidazolidine - Pyrimidone - Monoalkyl phosphate - Fatty amide - Hydropyrimidine - Pyrimidine - Imidazolidinone - N-acyl-amine - Fatty acyl - Organic phosphoric acid derivative - Alkyl phosphate - Phosphoric acid ester - Thiophene - Thiolane - Oxolane - Vinylogous amide - Heteroaromatic compound - Imidazolidine - Carboxamide group - Lactam - Urea - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkylthioether - Thioether - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Aromatic heteropolycyclic 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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