Compound Identification
SMILES
CCC1OC(=O)C(C)C(O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@@H](C)O2)C(C)[C@@H](O[C@@H]2O[C@H](C)C[C@H]([C@H]2O)[N+](C)(C)CC=C)[C@]2(C)CC(C)=C(O2)[C@H](C)[C@@H](O)[C@]1(C)O
InChIKey
InChIKey=VXWADTPWCZAPAE-VDSVTQHLSA-N
Formula
C40H70NO12
Mass
756.994
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
-
Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Aminosaccharides
- Level 6 Aminoglycosides
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Level 5
Aminosaccharides
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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
Aminosaccharides
Direct Parent
Aminoglycosides
Alternative Parents
O-glycosyl compounds Oxanes Monosaccharides Tetraalkylammonium salts Tertiary alcohols Dihydrofurans Secondary alcohols 1,2-aminoalcohols Carboxylic acid esters Lactones Oxacyclic compounds Acetals Dialkyl ethers Monocarboxylic acids and derivatives Carbonyl compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds Organic cations
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Aminoglycoside core - Glycosyl compound - O-glycosyl compound - Monosaccharide - Oxane - Tetraalkylammonium salt - Dihydrofuran - Tertiary alcohol - Quaternary ammonium salt - 1,2-aminoalcohol - Carboxylic acid ester - Lactone - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Alcohol - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organopnictogen compound - Carbonyl group - Organonitrogen compound - Organic cation - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.
External Descriptors
Not available