Compound Identification
SMILES
NC(=S)C1=NNC([C@@H]2O[C@H](COCC3=CC=CC=C3)[C@@H](OCC3=CC=CC=C3)[C@H]2OCC2=CC=CC=C2)=C1N
InChIKey
InChIKey=GWCODYUWPFEMSU-HYJYBNJOSA-N
Formula
C30H32N4O4S
Mass
544.67
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 Benzylethers Thioamides Pyrazoles Oxolanes Heteroaromatic compounds Thiocarboxylic acid amides Oxacyclic compounds Dialkyl ethers Azacyclic compounds Thiocarbonyl compounds Primary amines Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
3-ribofuranosylpyrazole - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Benzylether - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Heteroaromatic compound - Azole - Thioamide - Pyrazole - Oxolane - Oxacycle - Azacycle - Organoheterocyclic compound - Thiocarboxylic acid amide - Dialkyl ether - Ether - Hydrocarbon derivative - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Amine - Primary amine - Thiocarbonyl group - 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