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1-Methylpyridinio-3-carboxylat

Trigonelline

HCID 5570
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Grundinformationen

CAS
535-83-1
Standard-SMILES
C[n+]1cccc(C(=O)[O-])c1
InChIKey
WWNNZCOKKKDOPX-UHFFFAOYSA-N
Summenformel
C7H7NO2
Durchschnittliche Molmasse
137,138 g/mol
Monoisotopische Masse
137,04767846

Namen und Bezeichner

Bevorzugter Name
Trigonelline
IUPAC
1-Methylpyridin-1-ium-3-carboxylate
Lokaler Name
1-Methylpyridinio-3-carboxylat
Englischer Name
Trigonelline
Summenformel
C7H7NO2
Molmasse
137.14

Namen und Synonyme

GynesineN-MethylnicotinateTrigonellinTrigonelineCaffearineGynesisCoffearinCoffearineTrigenollineTRIGONELLINE

Datenbank-Bezeichner

CAS
535-83-1
PubChem CID
5570
DTXSID
DTXSID2026230
ChEMBL
CHEMBL350675
ChEBI
CHEBI:18123
UNII
3NQ9N60I00
EC Number
208-620-5
Nikkaji
J6.346K

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
260 °C · 260°C (dec.)
Siedepunkt
251.96 °C · 251.96°C (rough estimate)
Dichte
1.2528 · 1.2528 (rough estimate)
Brechungsindex
1.503 · 1.5030 (estimate)
storage temp.
Refrigerator
Löslichkeit
Methanol (Slightly), Water (Slightly)
Aggregatzustand
Solid
Farbe
Off-White to Light Beige
Major Application
pharmaceutical (small molecule)
InChI
InChI=1S/C7H7NO2/c1-8-4-2-3-6(5-8)7(9)10/h2-5H,1H3
InChIKey
WWNNZCOKKKDOPX-UHFFFAOYSA-N
SMILES
C1(C([O-])=O)=CC=C[N+](C)=C1
LogP
-3.91 · -3.910 (est)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

wgk
WGK 3
tsca
TSCA listed
hs_code
29339900
safety_code
24/25
Speicherklasse
13 - Non Combustible Solids
Giftige Stoffe Daten
535-83-1(Hazardous Substances Data)

Chemie und Industrie

Anwendungen · 3 Einträge

BeschreibungTrigonelline is a bitter alkaloid in coffee which serves to produce important aroma compounds. In terms of concentration trigonelline is higher for arabica than robusta and ranges from about 0.6-1.3% and 0.3-0.9%, respectively. Trigonelline, the N-methylpyridinium-3-carboxylate, is, after caffeine, the second most important alkaloid of coffee, with about 1% of the green bean. During leaf development, it is synthesized in the leaves and in the fruits' pericarp and accumulated in the seeds. The direct precursors are nicotinic acid and nicotine amide, deriving from the pyridine nucleotide cycle. Trigonelline is a plant hormone that has diverse regulatory functions with respect to plant cell cycle regulation, nodulation, and oxidative stress, and in helping survival and growth of the plant. It is found in significant quantity in many plants like coffee beans and fenugreek seed. Because it was first isolated from the fenugreek seeds (Trigonella foenum-graecum), the name assigned to it has been “trigonelline.” The chemical formula for trigonelline is C7H7NO2. It is a methylation product of niacin (vitamin B3), and thus is also known as “methylated niacin.” At higher temperatures, trigonelline breaks down to niacin. In addition to trigonelline, fenugreek seeds contain other alkaloids such as gentianine and carpaine.

OccurrenceTrigonelline (TRG) is a plant alkaloid mainly obtained from fenugreek (Trigonella foenum-graecum L.) seeds. Apart from this, it is also reported to be present in other plant species such as tree onion or Allium cepa, Coffea sp., pea or Pisum sativum, Soybean or Glycine max, and tomato or Lycopersicon esculentum.

Verwendenantihyperglycemic. Trigonelline is an inhibitor which, like abscicic acid, accumulates in plant cells when the plant becomes dormant or is exposed to stress. This natural inhibitor is chemically related to glycine betaine. It has been found in dormant winter buds of Populus trichocarpa * deltoides trees in the field as well as in salt-stressed micropropagules thereof. Some trigonelline also occurred in non-stressed micropropagules, probably as the result of bioconversion of niacin taken up from the nutrient medium (Bray et al. 1988). Trigonelline preferentially promotes arrest in G2 of the cell cycle and appears to have a growth controlling function during seed germination (Evans and Tramontano 1981).

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Vorgelagerte Rohstoffe

1-MethylpyridiniumchloridKohlenstoffdioxidKohlenstoff1-Methylpyrrol

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Ergänzende Hinweise

DefinitionChEBI: An iminium betaine that is the conjugate base of N-methylnicotinic acid, arising from deprotonation of the carboxy group.