Structure via PubChem · Public domain (PubChem)
fisetinidin
Sign in to saveFisetinidin is an anthocyanidin. It has been obtained from the heartwood of Acacia mearnsii, from the bark of Rhizophora apiculata and can also be synthesized. Fisetinidin is very similar in structure to fisetin, which itself differs in structure from quercetin only by an additional hydroxyl group on the latter.
In the Vinony graph
Within Vinony's link graph, fisetinidin is referenced by 52 other articles, and connects out to delphinidin chloride, digital object identifier and chemical formula.
It is catalogued under topics including Anthocyanidins, Catechols and Chembox image size set.
Its subject is documented across 7 Wikipedia language editions.
Chemical data
- Formula
- C15H11ClO5
- Molecular weight
- 306.7 g/mol
- IUPAC name
- 2-(3,4-dihydroxyphenyl)chromenylium-3,7-diol chloride
- SMILES
- C1=CC(=CC2=[O+]C(=C(C=C21)O)C3=CC(=C(C=C3)O)O)O.[Cl-]
- InChIKey
- GLSBVYMMIPVYDC-UHFFFAOYSA-N
- Polar surface area
- 81.9 Ų
- H-bond donors
- 4
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- cation
- Mass
- 306.029501
Show 3 more facts
- canonical SMILES
- C1=CC(=CC2=[O+]C(=C(C=C21)O)C3=CC(=C(C=C3)O)O)O.[Cl-]
- chemical formula
- C₁₅H₁₁ClO₅
- Commons category
- Fisetinidin
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Tannins
- See also
- References
Fisetinidin is an anthocyanidin. It has been obtained from the heartwood of Acacia mearnsii, from the bark of Rhizophora apiculata and can also be synthesized. Fisetinidin is very similar in structure to fisetin, which itself differs in structure from quercetin only by an additional hydroxyl group on the latter.
An assay of twenty flavonoids showed fisetinidin to be the least effective in inhibition of CD38 enzyme.
Excerpted from Wikipedia’s “fisetinidin” article, available under the CC BY-SA 4.0 licence.