Compound Identification
SMILES
CN(C1C2CN3CCC(O2)C13)C(=O)C1CC1
InChIKey
InChIKey=FXYHMIWPEOUVQP-UHFFFAOYSA-N
Formula
C12H18N2O2
Mass
222.288
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
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
Pyrrolizidines 1,4-oxazepines Cyclopropanecarboxylic acids and derivatives Morpholines N-alkylpyrrolidines Tetrahydrofurans Tertiary carboxylic acid amides Amino acids and derivatives Trialkylamines Azacyclic compounds Dialkyl ethers Oxacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Loline - Pyrrolizidine - Para-oxazepine - Cyclopropanecarboxylic acid or derivatives - Morpholine - Oxazinane - N-alkylpyrrolidine - Pyrrolidine - Tertiary carboxylic acid amide - Tetrahydrofuran - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Amine - Organopnictogen compound - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - 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