Compound Identification
SMILES
NC(=O)C1=NNC(C2OC(CO)C(O)C2O)=C1N
InChIKey
InChIKey=QZQFIZKWUMFPPU-UHFFFAOYSA-N
Formula
C9H14N4O5
Mass
258.234
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 3-ribofuranosylpyrazoles
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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
3-ribofuranosylpyrazoles
Intermediate Tree Nodes
Not available
Direct Parent
3-ribofuranosylpyrazoles
Alternative Parents
C-glycosyl compounds Pentoses Pyrazole-5-carboxamides 2-heteroaryl carboxamides Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Primary carboxylic acid amides Amino acids and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
3-ribofuranosylpyrazole - Glycosyl compound - C-glycosyl compound - Pentose monosaccharide - 2-heteroaryl carboxamide - Pyrazole-5-carboxamide - Monosaccharide - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Pyrazole - Azole - Secondary alcohol - Primary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 3-ribofuranosylpyrazoles. These are nucleoside and nucleotide analogs with a structure that consists of a pyrazole ring system which is N-substituted at the 3-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
External Descriptors
Not available