Classification Term: 169615

Tetrahydropyridines (ontology term: 2473f5b1fae59ba35873d58d8731c8ec)

found 7 associated metabolites at sub_class metabolite taxonomy ontology rank level.

Ancestor: Hydropyridines

Child Taxonomies: There is no child term of current ontology term.

Arecaidine

3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-methyl-

C7H11NO2 (141.0789746)


Arecaidine is a citraconoyl group. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2]. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2]. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2].

   

Arecaidine

3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-methyl-

C7H11NO2 (141.0789746)


Arecaidine is found in nuts. Arecaidine is an alkaloid from nuts of Areca catechu (betel nuts Arecaidine is a citraconoyl group. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2]. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2]. Arecaidine, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine is a substrate of H+-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake[1][2].

   

gamma-Coniceine

gamma-Coniceine

C8H15N (125.120443)


   

Albine

1,5-Methano-10H-pyrido[1,2-a][1,5]diazocin-10-one,1,2,3,4,5,6,11,11a-octahydro-2-(2-propen-1-yl)-, (1S,2R,5R,11aR)-

C14H20N2O (232.157555)


   

6-Acetyl-1,2,3,4-tetrahydropyridine

Methyl 3,4,5,6-tetrahydro-2-pyridyl ketone, 8ci

C7H11NO (125.0840596)


6-Acetyl-1,2,3,4-tetrahydropyridine is found in cereals and cereal products. Responsible for mousy taint in wines. 6-Acetyl-1,2,3,4-tetrahydropyridine is a constituent of wheat, popcorn and bread aroma 6-Acetyl-2,3,4,5-tetrahydropyridine is a substituted tetrahydropyridine and a cyclic imine as well as a ketone. The compound exists in a chemical equilibrium with its tautomer 6-acetyl-1,2,3,4-tetrahydropyridine that differs only by the position of the double bond in the tetrahydropyridine ring:; 6-Acetyl-2,3,4,5-tetrahydropyridine, with the IUPAC name 1-(3,4,5,6-tetrahydropyridin-2-yl)ethanone, is an aroma compound and flavor that gives baked goods such as white bread, pop corn, or tortillas their typical smell, together with its structural homolog 2-acetyl-1-pyrroline

   

(S)-1-piperideine-6-carboxylic acid

(S)-2,3,4,5-Tetrahydropyridine-2-carboxylic acid

C6H9NO2 (127.0633254)


The (S)-enantiomer of 1-piperideine-6-carboxylic acid.

   

Acetyltetrahydropyridine

Acetyltetrahydropyridine

C7H11NO (125.0840596)