35:
614:
Vitrac, X.; Bornet, A. L.; Vanderlinde, R.; Valls, J.; Richard, T.; Delaunay, J. C.; Mérillon, J. M.; Teissédre, P. L. (2005). "Determination of
Stilbenes (δ-viniferin, trans-astringin, trans-piceid, cis- and trans-resveratrol, ε-viniferin) in Brazilian Wines".
686:
González-Barrio, R. O.; Beltrán, D.; Cantos, E.; Gil, M. A. I.; Espín, J. C.; Tomás-Barberán, F. A. (2006). "Comparison of Ozone and UV-C Treatments on the
Postharvest Stilbenoid Monomer, Dimer, and Trimer Induction in Var. 'Superior' White Table Grapes".
650:
Timperio, A. M.; d’Alessandro, A.; Fagioni, M.; Magro, P.; Zolla, L. (2012). "Production of the phytoalexins trans-resveratrol and delta-viniferin in two economy-relevant grape cultivars upon infection with
Botrytis cinerea in field conditions".
120:
834:
Wilkens, A.; Paulsen, J.; Wray, V.; Winterhalter, P. (2010). "Structures of Two Novel
Trimeric Stilbenes Obtained by Horseradish Peroxidase Catalyzed Biotransformation oftrans-Resveratrol and (−)-ε-Viniferin".
764:
Santamaria, A. R.; Mulinacci, N.; Valletta, A.; Innocenti, M.; Pasqua, G. (2011). "Effects of
Elicitors on the Production of Resveratrol and Viniferins in Cell Cultures ofVitis viniferaL. Cv Italia".
544:
Pezet, R.; Perret, C.; Jean-Denis, J. B.; Tabacchi, R.; Gindro, K.; Viret, O. (2003). "Δ-Viniferin, a
Resveratrol Dehydrodimer: One of the Major Stilbenes Synthesized by Stressed Grapevine Leaves".
579:
Waffo-Teguo, P.; Lee, D.; Cuendet, M.; Mérillon, J. M.; Pezzuto, J. M.; Kinghorn, A. D. (2001). "Two New
Stilbene Dimer Glucosides from Grape (Vitisvinifera) Cell Cultures".
479:
Shikishima, Y.; Takaishi, Y.; Honda, G.; Ito, M.; Takeda, Y.; Kodzhimatov, O. K.; Ashurmetov, O. (2001). "Phenylbutanoids and stilbene derivatives of Rheum maximowiczii".
799:
Szewczuk, L. M.; Lee, S. H.; Blair, I. A.; Penning, T. M. (2005). "Viniferin
Formation by COX-1: Evidence for Radical Intermediates during Co-oxidation of Resveratrol".
524:"ChemIDplus - 0204076788 - LILPTCHQLRKZNG-CKKRXTSSSA-N - delta-Viniferin - Similar structures search, synonyms, formulas, resource links, and other chemical information"
228:
InChI=1S/C28H22O6/c29-20-6-4-18(5-7-20)28-27(19-12-23(32)15-24(33)13-19)25-11-16(3-8-26(25)34-28)1-2-17-9-21(30)14-22(31)10-17/h1-15,27-33H/b2-1+/t27-,28+/m1/s1
981:
244:
873:
379:, a pathogen responsible for the black dead arm disease of grapevine, has also been shown to be able to oxidise wood δ-resveratrol into delta-viniferin.
904:
219:
961:
976:
966:
351:
308:
897:
430:
724:"Identification of phytotoxins from Botryosphaeria obtusa, a pathogen of black dead arm disease of grapevine"
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337:) leaves. It is also found in plant cell cultures and wine. It can also be found in
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C1=CC(=CC=C12(C3=C(O2)C=CC(=C3)/C=C/C4=CC(=CC(=C4)O)O)C5=CC(=CC(=C5)O)O)O
192:
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Djoukeng, J. D. S.; Polli, S.; Larignon, P.; Abou-Mansour, E. (2009).
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52:
5--2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol
301:
Except where otherwise noted, data are given for materials in their
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331:. It can be isolated from stressed grapevine (
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837:Journal of Agricultural and Food Chemistry
766:Journal of Agricultural and Food Chemistry
689:Journal of Agricultural and Food Chemistry
617:Journal of Agricultural and Food Chemistry
546:Journal of Agricultural and Food Chemistry
401:Delta-viniferin can also be produced from
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26:
539:
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231:Key: LILPTCHQLRKZNG-CKKRXTSSSA-N
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139:
7:
917:(molecules with a C6-C2-C6 backbone)
982:Heterocyclic compounds with 2 rings
731:European Journal of Plant Pathology
195:
409:(COX-1, cyclooxygenase-1) or from
25:
653:Plant Physiology and Biochemistry
33:
305:(at 25 °C , 100 kPa).
360:, the agent of downy mildew),
1:
501:10.1016/S0031-9422(00)00370-8
382:In cell cultures, the use of
665:10.1016/j.plaphy.2011.07.008
801:Journal of Natural Products
581:Journal of Natural Products
998:
878:at Schroeder group website
874:Stilbenoids isolated from
295:454.47 g/mol
743:10.1007/s10658-008-9419-6
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260:
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58:
46:
41:
32:
431:Phenolic content in wine
350:following stresses like
323:is a resveratrol dehydro
394:stimulates δ-viniferin
419:horseradish peroxidase
962:Resveratrol oligomers
413:-resveratrol and (−)-
376:Botryosphaeria obtusa
327:. It is an isomer of
48:Preferred IUPAC name
977:Oxygen heterocycles
522:Chambers, Michael.
493:2001PChem..56..377S
357:Plasmopara viticola
29:
930:Dihydrostilbenoids
346:It is a grapevine
340:Rheum maximowiczii
309:Infobox references
27:
967:Stilbenoid dimers
949:
948:
849:10.1021/jf100606p
843:(11): 6754–6761.
813:10.1021/np049702i
778:10.1021/jf201181n
772:(17): 9094–9101.
701:10.1021/jf060160f
695:(12): 4222–4228.
629:10.1021/jf050122g
623:(14): 5664–5669.
593:10.1021/np000426r
558:10.1021/jf030227o
552:(18): 5488–5492.
415:epsilon-viniferin
329:epsilon-viniferin
317:Chemical compound
315:
314:
121:Interactive image
16:(Redirected from
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936:Hydroxystilbenes
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384:methyl jasmonate
352:fungal infection
268:Chemical formula
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18:Delta-viniferin
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481:Phytochemistry
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72:)-dehydrodimer
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68:Resveratrol (
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972:Phytoalexins
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807:(1): 36–42.
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457:R2-Viniferin
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396:biosynthesis
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80:Identifiers
69:
66:-δ-Viniferin
63:
59:Other names
28:δ-Viniferin
932:(Bibenzyls)
915:stilbenoids
452:R-Viniferin
447:ε-Viniferin
442:α-Viniferin
403:resveratrol
371:treatment.
365:irradiation
348:phytoalexin
321:δ-Viniferin
261:Properties
141:CHEBI:76147
97:204076-78-8
61:δ-Viniferin
956:Categories
737:(2): 303.
463:References
291:Molar mass
172:ChemSpider
108:3D model (
87:CAS Number
436:Viniferin
405:by human
392:elicitors
74:Maximol A
913:Type of
857:20455561
821:15679314
786:21751812
751:37168306
709:16756350
673:21821423
637:15998130
601:11170689
566:12926902
509:11249105
425:See also
362:UV light
489:Bibcode
285:
193:PubChem
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245:SMILES
206:637098
181:552752
152:ChEMBL
42:Names
923:Types
747:S2CID
727:(PDF)
411:trans
407:PTGS1
369:ozone
325:dimer
220:InChI
132:ChEBI
110:JSmol
64:trans
853:PMID
817:PMID
782:PMID
705:PMID
669:PMID
633:PMID
597:PMID
562:PMID
505:PMID
386:and
354:(by
845:doi
809:doi
774:doi
739:doi
735:124
697:doi
661:doi
625:doi
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554:doi
497:doi
417:by
390:as
367:or
196:CID
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281:O
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70:E
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