Structure Information
Structure

Compound Identification

SMILES

CN([C@@H]1[C@@H]2CN3CC[C@@H](O2)C13)C(=O)C1CC1

InChIKey

InChIKey=FXYHMIWPEOUVQP-GZBOUJLJSA-N

Formula

C12H18N2O2

Mass

222.288

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Loline alkaloids and derivatives

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Loline alkaloids and derivatives

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Loline - Pyrrolizidine - Para-oxazepine - Cyclopropanecarboxylic acid or derivatives - Morpholine - Oxazinane - N-alkylpyrrolidine - Oxolane - Pyrrolidine - Tertiary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Ether - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as loline alkaloids and derivatives. These are alkaloids with a structure characterized by a saturated pyrrolizidine ring, a primary amine at the C-1 carbon, and an internal ether bridge joining two distant ring (C-2 and C-7) carbons. Different substituents at the C-1 amine, such as methyl, formyl, and acetyl groups, yield various loline species.

External Descriptors

Not available

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