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Structure Information
Structure

Compound Identification

SMILES

CC1=CC(=O)NC(=O)N1C1CCC(C1)OCOP(O)(=O)OP(O)(=O)NP(O)(=O)OP(O)(=O)COC1CCC(C1)N1C(C)=CC(=O)NC1=O

InChIKey

InChIKey=XNODBUBJBNTIOI-UHFFFAOYSA-N

Formula

C22H35N5O17P4

Mass

765.435

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Phosphonated cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted phosphonated cyclopentyl nucleosides

Direct Parent

1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

1,3-substituted phosphonated cyclopentyl pyrimidine nucleoside - Monoalkyl phosphate - Pyrimidone - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Organophosphonic acid - Organophosphonic acid derivative - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organophosphorus compound - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 3-position with either a pyrimidine base.

External Descriptors

Not available

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