Compound Identification
SMILES
CC(C)(C)OC(=O)N1CCCN(CCN(CCCN(CC1)C(=O)CCCC(=O)OC[C@H]1O[C@H](CS1)N1C=CC(N)=NC1=O)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
InChIKey
InChIKey=AFTIVDZUPCICFU-VEEOACQBSA-N
Formula
C38H63N7O11S
Mass
826.02
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
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
Pyrimidones Aminopyrimidines and derivatives Fatty acid esters Imidolactams Hydropyrimidines Tertiary carboxylic acid amides Oxathiolanes Carbamate esters Monothioacetals Heteroaromatic compounds Carboxylic acid esters Organic carbonic acids and derivatives Azacyclic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Carbonyl compounds Organic oxides Primary amines Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Aminopyrimidine - Fatty acid ester - Pyrimidone - Hydropyrimidine - Fatty acyl - Imidolactam - Pyrimidine - Heteroaromatic compound - Monothioacetal - Carbamic acid ester - Tertiary carboxylic acid amide - Oxathiolane - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Carbonic acid derivative - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organopnictogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteromonocyclic 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