Compound Identification
SMILES
CNC1=NC=NC2=C1C=NN2C1OC(CO)C(O)C1O
InChIKey
InChIKey=SMRWSRKPYDUHBY-UHFFFAOYSA-N
Formula
C11H15N5O4
Mass
281.272
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrazolo[3,4-d]pyrimidine glycosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrazolo[3,4-d]pyrimidine glycosides
Alternative Parents
Glycosylamines Pentoses Pyrazolo[3,4-d]pyrimidines Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Tetrahydrofurans Pyrazoles Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrazolo[3,4-d]pyrimidine glycoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrazolo[3,4-d]pyrimidine - Pyrazolopyrimidine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monosaccharide - Imidolactam - Pyrimidine - Azole - Heteroaromatic compound - Pyrazole - Tetrahydrofuran - Secondary alcohol - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyrazolo[3,4-d]pyrimidine glycosides. These are nucleosides or derivatives thereof that consist of a pyazolo[3,2-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.
External Descriptors
Not available