CC1C(O)O[C@H](CO)[C@@H](OC2C[C@H](O)C(OC3OC(CO)C(OC4OC[C@@](O)(O[C@]5(CC(O)[C@H](N)CO5)C(O)=O)C(CO)[C@H]4O)C(O)[C@H]3O)C(CO)O2)[C@H]1O

InChIKey=JEEFNFNBWZFLRQ-ZTLYLITRSA-N

C31H53NO23

807.749

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Sugar acids and derivatives - Sugar amino acids and derivatives

Pyranoid amino acids and derivatives

Delta amino acids and derivatives O-glycosyl compounds Disaccharides Ketals Pyrans Oxanes Secondary alcohols 1,2-aminoalcohols Amino acids Hemiacetals Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Hydrocarbon derivatives Monoalkylamines Organic oxides Carbonyl compounds Organopnictogen compounds Primary alcohols

Aliphatic heteromonocyclic compounds

Pyranoid amino acid - Delta amino acid or derivatives - Disaccharide - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Pyran - 1,2-aminoalcohol - Amino acid or derivatives - Hemiacetal - Amino acid - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Amine - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Alcohol - Primary aliphatic amine - Carbonyl group - Primary alcohol - Primary amine - Organonitrogen compound - Hydrocarbon derivative - Aliphatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as pyranoid amino acids and derivatives. These are compounds containing a (hydro)pyran ring bearing unprotected amino and carboxylic acid functionalities.

Not available