Compound Identification
SMILES
CN(C)CCNC(=O)C1=CC2=C(C=C1)N=C(N2)[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
InChIKey
InChIKey=SQGOIUFLGQEHRW-LYYZXLFJSA-N
Formula
C18H26N4O6
Mass
394.428
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 2-pyranosylbenzimidazoles
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Class
Nucleoside and nucleotide analogues
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
2-pyranosylbenzimidazoles
Intermediate Tree Nodes
Not available
Direct Parent
2-pyranosylbenzimidazoles
Alternative Parents
Hexoses C-glycosyl compounds Benzimidazoles Benzenoids Oxanes Imidazoles Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides Trialkylamines 1,2-diols Amino acids and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-pyranosylbenzimidazole - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - Benzimidazole - Monosaccharide - Benzenoid - Oxane - Azole - Heteroaromatic compound - Imidazole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Amine - Organic oxide - Organooxygen compound - Alcohol - Organonitrogen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2-pyranosylbenzimidazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzimidazole which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
External Descriptors
Not available