Compound Identification
SMILES
CN(C)C=NC(O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)C1=NC=C(N1)C(N)=O
InChIKey
InChIKey=TVLIHOIPOLTNLD-BIDHKMRASA-N
Formula
C12H19N5O5
Mass
313.314
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
C2-linked imidazole ribonucleosides and ribonucleotides
Intermediate Tree Nodes
Not available
Direct Parent
C2-linked imidazole ribonucleosides and ribonucleotides
Alternative Parents
C-glycosyl compounds 2-heteroaryl carboxamides Carbonylimidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Amino acids and derivatives Tertiary amines Primary carboxylic acid amides Oxacyclic compounds Formamidines Dialkyl ethers Carboximidamides Carboxamidines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Alkanolamines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
C2-linked imidazole ribonucleoside - C-glycosyl compound - Glycosyl compound - 2-heteroaryl carboxamide - Imidazole-4-carbonyl group - Azole - Heteroaromatic compound - Imidazole - Oxolane - 1,2-diol - Amino acid or derivatives - Carboxamide group - Primary carboxylic acid amide - Secondary alcohol - Tertiary amine - Alkanolamine - Amidine - Formamidine - Carboxylic acid amidine - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Alcohol - Amine - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as c2-linked imidazole ribonucleosides and ribonucleotides. These are nucleoside and nucleotide analogues with a structure that consists of an imidazole ring system which is substituted at the C2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
External Descriptors
Not available