Structure Information
Structure

Compound Identification

SMILES

NC(N)=NCCC(=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(=O)NC1=O

InChIKey

InChIKey=XPMMONGFUUCRED-FOBYXSAKSA-N

Formula

C13H23N6O15P3

Mass

596.275

Export to:

JSON SDF CSV

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 - Glycosyl compound - N-glycosyl compound - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Guanidine - Lactam - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Carboximidamide - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - 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

Previous Back Next