Compound Identification
SMILES
CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.C[C@H](OC[C@]1(CN(C(=O)N1)P(O)(O)=O)C1=CC=CC=C1)C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F
InChIKey
InChIKey=VJYKOGFKCVYXDR-BUEHIJGMSA-N
Formula
C34H53F6N4O15P
Mass
902.775
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
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Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Monosaccharides
- Level 6 Hexoses
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Level 5
Monosaccharides
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Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Monosaccharides
Direct Parent
Hexoses
Alternative Parents
Phenylimidazolidines Trifluoromethylbenzenes Benzylethers Organic phosphoric acids and derivatives Imidazolidinones 1,3-aminoalcohols Secondary alcohols 1,2-aminoalcohols 1,2-diols Azacyclic compounds Dialkylamines Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Alkyl fluorides Organic oxides Organofluorides Primary alcohols
Molecular Framework
Not available
Substituents
Hexose monosaccharide - Phenylimidazolidine - Trifluoromethylbenzene - Benzylether - Monocyclic benzene moiety - Imidazolidinone - Organic phosphoric acid derivative - Benzenoid - Imidazolidine - 1,3-aminoalcohol - Secondary alcohol - 1,2-aminoalcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Secondary amine - Dialkyl ether - Secondary aliphatic amine - Ether - Polyol - Alkyl fluoride - Alcohol - Carbonyl group - Organic nitrogen compound - Primary alcohol - Alkyl halide - Organic oxide - Amine - Hydrocarbon derivative - Organohalogen compound - Organonitrogen compound - Organofluoride - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
External Descriptors
Not available