| Weight | 271.248 g/mol |
|---|---|
| Formula | C15H11O5+ |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
Luteolinidin (1154-78-5, 16975-93-2)
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- Sigma-Aldrich - Search for Luteolinidin
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- Phytoalexin accumulation in sorghum : identification of a methyl ether of luteolinidin (Physiological and Molecular Plant Pathology, 1996)
- Synthesis of anthocyanidins-III1: Total synthesis of apigeninidin and luteolinidin chlorides (Tetrahedron, 1977)
- Photochemistry of luteolinidin: Write-lock-read-unlock-erase with a natural compound (Journal of Photochemistry and Photobiology A-chemistry, 2000)
- Micelle effects on multistate/multifunctional systems based on photochromic flavylium compounds. The case of luteolinidin (Journal of Molecular Structure, 2002)
- A New and Convenient One-StepSynthesis of the Natural 3-Deoxyanthocyanidins Apigeninidinand Luteolinidin Chlorides from 2,4,6-Triacetoxybenzaldehyde (Synthesis, 2003)
- 1H and 13C NMR assignments for the 3deoxyanthocyanins, luteolinidin5glucoside and apigeninidin5glucoside (Magnetic Resonance in Chemistry, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2)O)O)O)O
-
InChIKeyGDNIGMNXEKGFIP-UHFFFAOYSA-O
- Pubchem - Luteolinidin
- Wikipedia - luteolinidin cation
Luteolinidin is a chemical compound belonging to the 3-deoxyanthocyanidins and that can be found in Sorghum bicolor.
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