Structure Information
Structure

Compound Identification

SMILES

NCCCCC(N)C(=O)N[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1N1C=CC(N)=NC1=O

InChIKey

InChIKey=KHOMTNIDYJYBLO-QZBYRPAYSA-N

Formula

C15H29N6O14P3

Mass

610.346

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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 - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - N-acyl-amine - Imidolactam - Fatty acyl - Alkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Hydropyrimidine - Pyrimidine - Fatty amide - Heteroaromatic compound - Oxolane - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Primary amine - Alcohol - Hydrocarbon derivative - Primary aliphatic amine - Organonitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Amine - Organic oxygen compound - Organic nitrogen compound - 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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