Structure Information
Structure

Compound Identification

SMILES

CC[C@H](C)[C@@H]1NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC2=CN=CN2)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H](NC1=O)C(C)C)[C@@H](C)O)[C@@H](C)O)C(N)=O)C(C)C)C(C)C

InChIKey

InChIKey=FNYYZVKTLMJLHP-NEWCBHFCSA-N

Formula

C90H137N27O23

Mass

1965.252

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic Polymers

Class

Polypeptides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Polypeptides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Polypeptide - Cyclic alpha peptide - Alpha-amino acid or derivatives - 1,3-dicarbonyl compound - Monocyclic benzene moiety - Benzenoid - Pyrrolidine - Tertiary carboxylic acid amide - Imidazole - Azole - Heteroaromatic compound - Primary carboxylic acid amide - Lactam - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Guanidine - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Carboximidamide - Monocarboxylic acid or derivatives - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Imine - Organooxygen compound - Carbonyl group - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.

External Descriptors

Not available

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