Compound Identification
SMILES
CN1C(=NC2=CC=CC=C12)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
InChIKey
InChIKey=LSDWUCPCIWMCTK-DDHJBXDOSA-N
Formula
C13H19N2O13P3
Mass
504.217
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 2-ribofuranosylbenzimidazoles
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
2-ribofuranosylbenzimidazoles
Intermediate Tree Nodes
Not available
Direct Parent
2-ribofuranosylbenzimidazoles
Alternative Parents
Pentose phosphates C-glycosyl compounds Monosaccharide phosphates Benzimidazoles Monoalkyl phosphates N-substituted imidazoles Benzenoids Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-ribofuranosylbenzimidazole - Pentose phosphate - Pentose-5-phosphate - C-glycosyl compound - Glycosyl compound - Monosaccharide phosphate - Benzimidazole - Monoalkyl phosphate - Benzenoid - Alkyl phosphate - Phosphoric acid ester - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2-ribofuranosylbenzimidazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzimidazole ring system which is N-substituted at the 2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
External Descriptors
Not available