CC(C)[C@@H]1N(C)C(=O)[C@@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(O)=O)NC(=O)NNC(=O)[C@H](CCCN=C(N)N)NC1=O

InChIKey=UYLKMCAJPYTSGJ-GNBUJSLZSA-N

C26H39N9O7

589.654

Organic compounds

Organic acids and derivatives

Peptidomimetics

Azapeptides

Not available

Azapeptides

Oligopeptides Macrolactams Alpha amino acids and derivatives Benzene and substituted derivatives Tertiary carboxylic acid amides Semicarbazides Secondary carboxylic acid amides Carboxylic acid hydrazides Guanidines Lactams Organic carbonic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Carboximidamides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organic oxides

Aromatic heteromonocyclic compounds

Alpha-oligopeptide - Cyclic azapeptide fragment - Macrolactam - Alpha-amino acid or derivatives - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Semicarbazide - Carboxamide group - Carboxylic acid hydrazide - Guanidine - Lactam - Carbonic acid derivative - Secondary carboxylic acid amide - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as azapeptides. These are peptide analogues in which one or more of the amino residues is replaced by a semicarbazide.

Not available