Compound Identification
SMILES
C[NH2+][C@H]1[C@H]2CN3CC[C@H](O2)[C@H]13
InChIKey
InChIKey=OPMNROCQHKJDAQ-FKSUSPILSA-O
Formula
C8H15N2O
Mass
155.22
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 N-alkylpyrrolidines Morpholines Quaternary ammonium salts Oxolanes Trialkylamines Oxacyclic compounds Dialkylamines Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Organic cations
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Loline - Pyrrolizidine - Para-oxazepine - Morpholine - Oxazinane - N-alkylpyrrolidine - Oxolane - Pyrrolidine - Quaternary ammonium salt - Tertiary amine - Tertiary aliphatic amine - Secondary amine - Organoheterocyclic compound - Azacycle - Dialkyl ether - Oxacycle - Secondary aliphatic amine - Ether - Amine - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic cation - 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