Structure Information
Structure

Compound Identification

SMILES

CC(C)C[C@H](O)[C@@H](O)[C@H](CC1CCCCC1)C(=O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@@H](CC(=O)N1CCC(N)CC1)CC1=CC=CC=C1

InChIKey

InChIKey=FBARIPSRAMYMEQ-ANAOGEIGSA-N

Formula

C37H56N6O6

Mass

680.891

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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

Histidine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Histidine or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - N-acyl-piperidine - 4-aminopiperidine - Monocyclic benzene moiety - Piperidine - N-acyl-amine - Fatty amide - Benzenoid - Fatty acyl - Azole - Tertiary carboxylic acid amide - Carboxylic acid imide, n-unsubstituted - Dicarboximide - Imidazole - Carboxylic acid imide - Heteroaromatic compound - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Amine - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary aliphatic amine - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound

Description

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