Structure Information
Structure

Compound Identification

SMILES

CC(=O)SCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OCC1CCC(C1)N1C=NC2C1NCN=C2N

InChIKey

InChIKey=IMGKISXIQXVWGB-UHFFFAOYSA-N

Formula

C23H40N7O8PS

Mass

605.65

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Nucleoside and nucleotide analogues

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Beta amino acid or derivatives - Imidazopyrimidine - Dialkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - N-acyl-amine - Alkyl phosphate - Monosaccharide - Imidolactam - Fatty acyl - 1,2,5,6-tetrahydropyrimidine - Hydropyrimidine - Fatty amide - 2-imidazoline - N,s-acetal - Carboxamide group - Carbothioic s-ester - Tertiary amine - Secondary alcohol - Thiocarboxylic acid ester - Amino acid or derivatives - Secondary carboxylic acid amide - Amidine - Formamidine - Carboxylic acid amidine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Carboximidamide - Hemithioaminal - Secondary amine - Thiocarboxylic acid or derivatives - Carbonyl group - Alcohol - Organic oxygen compound - Amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

External Descriptors

Not available

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