[H][C@](N)(CCCCN=C(O)CCCC[C@]1([H])SC[C@]2([H])N=C(O)N[C@]12[H])C(O)=O

InChIKey=BAQMYDQNMFBZNA-MNXVOIDGSA-N

C16H28N4O4S

372.48

Organic compounds

Organic acids and derivatives

Carboxylic acids and derivatives

Amino acids, peptides, and analogues

Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids

L-alpha-amino acids

Imidazolyl carboxylic acids and derivatives Medium-chain fatty acids Heterocyclic fatty acids Thiolanes Imidazolines Amino acids Isoureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboximidamides Carboxylic acids Dialkylthioethers Monocarboxylic acids and derivatives Organopnictogen compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Monoalkylamines

Aliphatic heteropolycyclic compounds

L-alpha-amino acid - Imidazolyl carboxylic acid derivative - Medium-chain fatty acid - Heterocyclic fatty acid - Fatty acid - Fatty acyl - Thiolane - 2-imidazoline - Amino acid - Isourea - Azacycle - Carboximidic acid - Carboximidic acid derivative - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboxylic acid - Thioether - Monocarboxylic acid or derivatives - Organic oxide - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Organic oxygen compound - Primary amine - Organic nitrogen compound - Organopnictogen compound - Amine - Carbonyl group - Hydrocarbon derivative - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.

CHEBI:27870 : azabicycloalkane - ureas - thiabicycloalkane - monocarboxylic acid amide - non-proteinogenic L-alpha-amino acid - L-lysine derivative