Structure Information
Structure

Compound Identification

SMILES

OP(O)(=O)OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12)N1C=CC(=O)NC1=O

InChIKey

InChIKey=XYCDFLZYMIUTDO-OJFWXXFXSA-N

Formula

C19H29N4O16P3S

Mass

694.43

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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 - Biotin - Thienoimidazolidine - Fatty acid ester - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Imidazolidinone - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Fatty acyl - Thiophene - Thiolane - Vinylogous amide - Heteroaromatic compound - Imidazolidine - Oxolane - Carboxylic acid ester - Urea - Lactam - Organoheterocyclic compound - Thioether - Dialkylthioether - Azacycle - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - 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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