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Structure Information
Structure

Compound Identification

SMILES

ClC1=CC2=C(NC(=O)N[C@]2(C#CC2=CC=CC=N2)C2CC2)C=C1.CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=MPXNTEIGQVRADR-FOOXDCEFSA-N

Formula

C28H30ClN8O14P3

Mass

830.96

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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',3'-dideoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Not available

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside triphosphate - Quinazoline - Monoalkyl phosphate - Pyrimidone - Aryl chloride - Aryl halide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyridine - Hydropyrimidine - Benzenoid - Pyrimidine - Alkyl phosphate - Oxolane - Heteroaromatic compound - Vinylogous amide - Azo compound - Azo imide - Lactam - Urea - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organochloride - Organooxygen compound - Organohalogen compound - Organic salt - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleoside triphosphates. These are pyrimidine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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