:Hirsutidin
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 424926720
| Name = Hirsutidin
| ImageFile = Hirsutidin.svg
| ImageSize = 250px
| IUPACName = 3,4′,5-Trihydroxy-3′,5′,7-trimethoxyflavylium
| SystematicName = 3,5-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-1λ4-benzopyran-1-ylium
| OtherNames =
|Section1={{Chembox Identifiers
| index2_label = (chloride)
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 151776-57-7
| CASNo2_Ref = {{cascite|correct|CAS}}
| CASNo2 = 4092-66-4
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = VV9H579AR2
| UNII2_Ref = {{fdacite|correct|FDA}}
| UNII2 = UX37SFW7Y9
| PubChem = 441694
| SMILES = Oc1cc2c(O)cc(OC)cc2[o+]c1c3cc(OC)c(O)c(OC)c3
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 390303
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 5728
| InChI = 1/C18H16O7/c1-22-10-6-12(19)11-8-13(20)18(25-14(11)7-10)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1
| InChIKey = JGPCLGHKWGCWNO-IKLDFBCSAS
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C18H16O7/c1-22-10-6-12(19)11-8-13(20)18(25-14(11)7-10)9-4-15(23-2)17(21)16(5-9)24-3/h4-8H,1-3H3,(H2-,19,20,21)/p+1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = JGPCLGHKWGCWNO-UHFFFAOYSA-O
}}
|Section2={{Chembox Properties
| Formula = C18H17O7+
| MolarMass = 345.32 g/mol
| Appearance =
| Density =
| MeltingPt =
| BoilingPt =
| Solubility =
}}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
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Hirsutidin is an O-methylated anthocyanidin, a chemical compound belonging to the anthocyanins. It can be found in Catharanthus roseus[https://archive.today/20130105063940/http://www3.interscience.wiley.com/journal/5021/abstract?CRETRY=1&SRETRY=0 Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry, Anna Piovan, Raffaella Filippini, Donata Favretto, 1998] (Madagascar periwinkle) where it is the prominent compound in petals and can also be found in callus cultures.[http://www.biologie.uni-freiburg.de/data/bio2/schroeder/Plant_Catharanthus_Flavonoids.html Catharanthus flavonoids on Schroeder page, uni. Freiburg, Germany]
Glycosides
3-O-(6-O-p-coumaroyl) glucoside of hirsutidin can also be found in Catharanthus roseus.{{cite journal | url=https://doi.org/10.1007%2Fs11101-006-9052-y | doi=10.1007/s11101-006-9052-y | title=Anthocyanins in Catharanthus roseus in vivo and in vitro: A review | year=2007 | last1=Piovan | first1=Anna | last2=Filippini | first2=Raffaella | journal=Phytochemistry Reviews | volume=6 | issue=2–3 | pages=235–242 | bibcode=2007PChRv...6..235P | s2cid=676724 | url-access=subscription }}