Structure Information
Structure

Compound Identification

SMILES

CCCCCN(C(N)=N[C@@H](CC1=CC=C(NC(=O)C2=C(Cl)C=NC=C2Cl)C=C1)C(O)=O)C1=CC=CC=C1C(=O)NCC1CCCCC1

InChIKey

InChIKey=MNKVJHTVZSICKE-LJAQVGFWSA-N

Formula

C35H42Cl2N6O4

Mass

681.66

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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

Phenylalanine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenylalanine or derivatives - Aromatic anilide - Guanidinobenzoic acid or derivatives - 3-phenylpropanoic-acid - Amphetamine or derivatives - Benzamide - Benzoic acid or derivatives - Pyridine carboxylic acid or derivatives - Polyhalopyridine - Benzoyl - Aryl halide - Monocyclic benzene moiety - Pyridine - Benzenoid - Aryl chloride - Heteroaromatic compound - Vinylogous amide - Vinylogous halide - Carboxamide group - Guanidine - Secondary carboxylic acid amide - Carboximidamide - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organohalogen compound - Organochloride - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine 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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