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词条 Pelargonidin
释义

  1. Natural occurrences

      Presence in flowers    Presence in food  

  2. Glycosides

  3. See also

  4. References

  5. External links

{{chembox
| Verifiedfields = changed
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| verifiedrevid = 409412023
| ImageFile=pelargonidin.svg
| ImageSize=200px
| IUPACName=2-(4-Hydroxyphenyl)chromenylium-3,5,7-triol
| OtherNames=
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=134-04-3
| PubChem=440832
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 25863
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 1197905
| SMILES = C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)O)O)O
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 389676
| InChI = 1/C15H10O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-7H,(H3-,16,17,18,19)/p+1
| InChIKey = XVFMGWDSJLBXDZ-IKLDFBCSAF
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C15H10O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-7H,(H3-,16,17,18,19)/p+1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = XVFMGWDSJLBXDZ-UHFFFAOYSA-O
| KEGG_Ref = {{keggcite|changed|kegg}}
| KEGG = C05904
|Section2={{Chembox Properties
| Formula = C15H11O5+
| MolarMass = 271.24 g/mol
| Appearance=
| Density=
| MeltingPt=
| BoilingPt=
| Solubility=
|Section3={{Chembox Hazards
| MainHazards=
| FlashPt=
| AutoignitionPt =
}}Pelargonidin is an anthocyanidin, a type of plant pigment producing a characteristic orange color used in food and industrial dyes.[1]

Natural occurrences

Presence in flowers

Pelargonidin can be found in red geraniums (Geraniaceae). It is the predominant pigment causing the red coloration in the spathes of Philodendron (Araceae). The orange-coloured flowers of blue pimpernel (Anagallis monelli, Myrsinaceae) have a higher concentration of pelargonidin pigment.

Presence in food

Pelargonidin can be found in berries such as ripe raspberries and strawberries, as well as blueberries, blackberries, cranberries but also in saskatoon berries[2] and chokeberries. It is also found in plums and pomegranates. Pelargonidin gives red radishes their color.[3]

It is present in large amounts in kidney beans.[4]

Glycosides

Pelargonidin-3-O-glucoside (callistephin) can be found in strawberries.[5]

Acylated pelargonidin glycosides can be found in red-purple flowers of Ipomoea purpurea.[6]

See also

  • List of phytochemicals in food
  • List of compounds with carbon number 15

References

1. ^{{cite patent| country = United States| number = 6,767,999| status = granted| title = Anthocyantin coloring agent and method for the production thereof from organic matter | pubdate = Nov 01, 2001| gdate = July 27, 2004| fdate = Dec 21, 2001| pridate = Apr 26, 2000| inventor = Smirnov, Vitaly; Sidorov, Viktor; Smirnova, Valentina| class = U.S. 536/18.5| url = http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&Sect2=HITOFF&u=%2Fnetahtml%2FPTO%2Fsearch-adv.htm&r=1&p=1&f=G&l=50&d=PTXT&S1=pelargonidin.ABTX.&OS=abst/pelargonidin&RS=ABST/pelargonidin}}
2. ^{{Cite journal|doi=10.1300/J492v05n03_10|title=Compositional and Functional Properties of Saskatoon Berry and Blueberry|year=2005|last1=Mazza|first1=G.|journal=International Journal of Fruit Science|volume=5|issue=3|pages=101}}
3. ^{{cite book|author=Takeshi Nishio|editor=Takeshi Nishio, Hiroyasu Kitashiba|title=The Radish Genome|url=https://books.google.com/books?id=8JQ4DwAAQBAJ&pg=PA70|date=4 October 2017|publisher=Springer|isbn=978-3-319-59253-4|page=4}}
4. ^{{Cite journal|doi=10.1016/j.foodchem.2007.08.038|title=The polyphenolic profiles of common bean (Phaseolus vulgaris L.)|year=2008|last1=Lin|first1=Long-Ze|last2=Harnly|first2=James M.|last3=Pastor-Corrales|first3=Marcial S.|last4=Luthria|first4=Devanand L.|journal=Food Chemistry|volume=107|pages=399|url=https://naldc-legacy.nal.usda.gov/naldc/download.xhtml?id=11587&content=PDF}}
5. ^{{Cite journal |doi=10.1021/jf072000p |title=Bioavailability of Pelargonidin-3-O-glucoside and Its Metabolites in Humans Following the Ingestion of Strawberries with and without Cream |year=2008 |last1=Mullen |first1=William |last2=Edwards |first2=Christine A. |last3=Serafini |first3=Mauro |last4=Crozier |first4=Alan |journal=Journal of Agricultural and Food Chemistry |volume=56 |issue=3 |pages=713–9 |pmid=18211024}}
6. ^{{Cite journal|pmid=8987912|year=1996|last1=Saito|first1=N|last2=Tatsuzawa|first2=F|last3=Yokoi|first3=M|last4=Kasahara|first4=K|last5=Iida|first5=S|last6=Shigihara|first6=A|last7=Honda|first7=T|title=Acylated pelargonidin glycosides in red-purple flowers of Ipomoea purpurea|volume=43|issue=6|pages=1365–70|journal=Phytochemistry|doi=10.1016/s0031-9422(96)00501-8}}

External links

{{commonscat|Pelargonidin}}{{Anthocyanins}}

2 : Anthocyanidins|Resorcinols

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