Structure Information
Structure

Compound Identification

SMILES

CC(C)CC(NC(=O)C1=COC(=N1)C1=CC=C(N)C=C1)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=DPUBZMBBJWZSQO-UHFFFAOYSA-N

Formula

C22H23N5O5

Mass

437.456

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Leucine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Leucine or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Phenyl-1,3-oxazole - Anilide - Nitrobenzene - N-arylamide - Aniline or substituted anilines - 2-heteroaryl carboxamide - Nitroaromatic compound - 2,4-disubstituted 1,3-oxazole - Fatty acyl - Primary aromatic amine - Benzenoid - Fatty amide - Monocyclic benzene moiety - Oxazole - Heteroaromatic compound - Azole - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Oxacycle - Azacycle - Organic oxoazanium - Organic salt - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Organic zwitterion - Primary amine - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as leucine and derivatives. These are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

External Descriptors

Not available

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