Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@@H]2O[C@H](COP(O)(=O)OC3=CC=CC=C3)[C@@H](N=[N+]=[N-])[C@@H]2O)C(=O)NC1=O

InChIKey

InChIKey=DEEOMLABBQJVBV-GUIRCDHDSA-N

Formula

C16H18N5O8P

Mass

439.321

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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 monophosphates

Direct Parent

Pyrimidine 3'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 3'-deoxyribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Phenoxy compound - Pyrimidone - Monoalkyl phosphate - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Vinylogous amide - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Lactam - Azo imide - Azo compound - Azacycle - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic salt - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 3'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 3.

External Descriptors

Not available

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