Structure Information
Structure

Compound Identification

SMILES

CC[C@H](NC(=O)[C@@H]1C[C@@](C)(NC(=O)NC2=CC(OC)=C(OC)C(OC)=C2)C2=NC=C(NCC3=CC(=CC=C3)C(F)(F)F)C(=O)N12)B1O[C@@H]2C3CC(C[C@]2(C)O1)C3(C)C

InChIKey

InChIKey=AJWQFOMRLAWBAE-ONPFAHOLSA-N

Formula

C40H50BF3N6O8

Mass

810.68

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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

Direct Parent

Gamma amino acids and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Gamma amino acid or derivatives - N-phenylurea - Monoterpenoid - Aromatic monoterpenoid - Trifluoromethylbenzene - Nopinane monoterpenoid - Pyrimidinecarboxamide - Pyrrolopyrimidine - Methoxyaniline - Phenylmethylamine - Phenoxy compound - Phenol ether - Anisole - Benzylamine - Methoxybenzene - Pyrimidone - Aminopyrimidine - Aralkylamine - Alkyl aryl ether - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Heteroaromatic compound - 1,3,2-dioxaborolane - Boronic acid ester - Boronic acid derivative - Carboxamide group - Lactam - Urea - Secondary carboxylic acid amide - Secondary amine - Oxacycle - Azacycle - Ether - Organic metalloid salt - Organoheterocyclic compound - Organofluoride - Organonitrogen compound - Alkyl fluoride - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alkylborane - Organic metalloid moeity - Alkyl halide - Monoalkylborane - Amine - Organic oxygen compound - Organohalogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom.

External Descriptors

Not available

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