Compound Identification
SMILES
CN(CC1=CC=C(C=C1)C1=CC=CC=C1C1=NNN=N1)C(=O)[C@@H](CCC1=CC=CC=C1)NC(=O)CC(C)(C)N
InChIKey
InChIKey=ZQGCBCZYBLOLHU-AREMUKBSSA-N
Formula
C30H35N7O2
Mass
525.657
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic acids and derivatives
-
Class
Peptidomimetics
- Subclass Hybrid peptides
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Class
Peptidomimetics
-
Superclass
Organic acids and derivatives
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Peptidomimetics
Subclass
Hybrid peptides
Intermediate Tree Nodes
Not available
Direct Parent
Hybrid peptides
Alternative Parents
N-acyl-alpha amino acids and derivatives Biphenyls and derivatives Alpha amino acid amides Phenyltetrazoles and derivatives Beta amino acids and derivatives N-acyl amines Tertiary carboxylic acid amides Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Hybrid peptide - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Biphenyl - Phenyltetrazole - Beta amino acid or derivatives - Alpha-amino acid or derivatives - N-acyl-amine - Fatty amide - Monocyclic benzene moiety - Benzenoid - Fatty acyl - Tertiary carboxylic acid amide - Tetrazole - Heteroaromatic compound - Azole - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Amine - Primary amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.
External Descriptors
Not available