Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)CC2OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O)C(=O)NC1=O

InChIKey

InChIKey=UWESRYMWFYIOFF-PGHULITCSA-N

Formula

C20H31N4O21P3

Mass

756.396

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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 3'-deoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 3'-deoxyribonucleoside triphosphate - Alpha-amino acid ester - Tetracarboxylic acid or derivatives - Alpha-amino acid - Alpha-amino acid or derivatives - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Alkyl phosphate - Organic phosphoric acid derivative - Pyrimidine - Phosphoric acid ester - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - Urea - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Amino acid - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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