δ-Viniferin is a resveratrol dehydrodimer. It is an isomer of epsilon-viniferin. It can be isolated from stressed grapevine (Vitis vinifera) leaves. It is also found in plant cell cultures and wine. It can also be found in Rheum maximowiczii.
It is a grapevine phytoalexin following stresses like fungal infection (by Plasmopara viticola, the agent of downy mildew), UV light irradiation or ozone treatment.
Botryosphaeria obtusa, 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.
In cell cultures, the use of methyl jasmonate and jasmonic acid as elicitors stimulates δ-viniferin biosynthesis.
Delta-viniferin can also be produced from resveratrol by human PTGS1 (COX-1, cyclooxygenase-1) or from trans-resveratrol and (−)-epsilon-viniferin by horseradish peroxidase.
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InChI=1S/C21H18O5S/c1- 13- 11- 15(7- 9- 18(13) 22) 21(16- 8- 10- 19(23) 14(2) 12- 16) 17- 5- 3- 4- 6- 20(17) 27(24,25) 26- 21/h3- 12,22- 23H,1- 2H3 |
OBRMNDMBJQTZHV-UHFFFAOYSA-N |
Cc1cc(ccc1O)C1(OS(=O)(=O)c2ccccc12)c1ccc(O)c(C)c1 |
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acid-base indicator
An acid or base which exhibits a colour change on neutralization by the basic or acidic titrant at or near the equivalence point of a titration.
dye
two-colour indicator
A colour indicator that possesses a different colour on each side of the transition interval.
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View more via ChEBI Ontology
3,3- bis(4- hydroxy- 5- methylphenyl)- 2,1λ6- benzoxathiole- 1,1(3H)- dione
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3',3''-Dimethylphenolsulfonephthalein
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ChemIDplus
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Cresolsulfophthalein
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ChemIDplus
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NSC 7224
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ChemIDplus
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o-Cresol Red
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ChemIDplus
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o-Cresolsulfonephthalein
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ChemIDplus
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1733-12-6
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CAS Registry Number
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ChemIDplus
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343399
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Reaxys Registry Number
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Reaxys
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