Compound Identification
SMILES
O[C@]1(O[C@H](COCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1)C1=NC2=CC=CC=C2S1
InChIKey
InChIKey=ZVTLGQFPKOLCSS-XSZGSGIISA-N
Formula
C41H39NO6S
Mass
673.82
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 2-pyranosylbenzothiazoles
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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
2-pyranosylbenzothiazoles
Intermediate Tree Nodes
Not available
Direct Parent
2-pyranosylbenzothiazoles
Alternative Parents
Hexoses Benzylethers Benzothiazoles Oxanes Thiazoles Heteroaromatic compounds Hemiacetals Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-pyranosylbenzothiazole - Hexose monosaccharide - 1,3-benzothiazole - Benzylether - Monocyclic benzene moiety - Benzenoid - Oxane - Monosaccharide - Azole - Heteroaromatic compound - Thiazole - Hemiacetal - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2-pyranosylbenzothiazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzothiazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
External Descriptors
Not available