Weight | 137.138 g/mol |
---|---|
Formula | C7H7NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Trigonelline (535-83-1)
trigonelline chloride · trigonelline ion · trigonelline iodide
Score:
#845 in Biochemistry
,
#2265 in Biology
,
#2791 in Chemistry
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- CAFFEINE, TRIGONELLINE, CHLOROGENIC ACIDS AND SUCROSE DIVERSITY IN WILD COFFEA ARABICA L. AND C. CANEPHORA P. ACCESSIONS (Food Chemistry, 2001)
- Rhizobium meliloti Genes Encoding Catabolism of Trigonelline Are Induced under Symbiotic Conditions. (The Plant Cell, 1990)
- Acute Effects Of Decaffeinated Coffee And The Major Coffee Components Chlorogenic Acid And Trigonelline On Glucose Tolerance (Diabetes Care, 2009)
- Trigonelline and Stachydrine Released from Alfalfa Seeds Activate NodD2 Protein in Rhizobium meliloti. (Plant Physiology, 1992)
- Inhibition of the Nrf2 transcription factor by the alkaloid trigonelline renders pancreatic cancer cells more susceptible to apoptosis through decreased proteasomal gene expression and proteasome activity (Oncogene, 2013)
- HPLC/diode-array applied to the thermal degradation of trigonelline, nicotinic acid and caffeine in coffee (Food Chemistry, 2000)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - trigonelline chloride
- trigonelline ion
- trigonelline iodide
- trigonelline tosylate
-
SMILESC[N+]1=CC=CC(=C1)C(=O)[O-]
-
InChIKeyWWNNZCOKKKDOPX-UHFFFAOYSA-N
- Pubchem - Trigonelline
- Wikipedia - trigonelline
Trigonelline is an alkaloid with chemical formula C7H7NO2. It is a zwitterion formed by the methylation of the nitrogen atom of niacin (vitamin B3). Trigonelline is a product of niacin metabolism that is excreted in urine of mammals.
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