CC(=O)N[C@@H]1[C@H](C=C(O[C@H]1[C@H](N)[C@H](O)CO)C(O)=O)N=C(N)N

InChIKey=DQUPXJPWBBJBMZ-LUTUWXHWSA-N

C12H21N5O6

331.329

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

1,3-aminoalcohols Acetamides Secondary carboxylic acid amides Secondary alcohols 1,2-aminoalcohols 1,2-diols Amino acids Guanidines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidamides Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds Primary alcohols

Aliphatic heteromonocyclic compounds

Pyranoid amino acid - 1,3-aminoalcohol - Acetamide - 1,2-aminoalcohol - 1,2-diol - Amino acid - Amino acid or derivatives - Guanidine - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Primary alcohol - Primary amine - Carbonyl group - Hydrocarbon derivative - Amine - Alcohol - Organic oxide - Organopnictogen compound - 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