1981
DOI: 10.1016/0031-9422(81)80044-1
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Two novel stilbene phytoalexins from Arachis hypogaea

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Cited by 70 publications
(63 citation statements)
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“…The T. versicolor activity of chlorophorin, however, was similar to the other extractives. Isoprenoid substitution has been reported to significantly increase stilbene fungal activity (Kindl 1985;Aguamah et al 1981), but our data suggest that the increased activity is limited to certain fungi. The mechanism by which stilbenes inhibit wood-decaying fungi is probably different for isoprenoid-vs. nonisoprenoid-s bstituted stilbenes, and thus our prior structure-activity relationship (SAR) results on the inactivity of 4 / -substituted stilbenes (Schultz et al 1990) are not applicable to this 4'-isoprenoid stilbene.…”
Section: Bioactivitiescontrasting
confidence: 70%
“…The T. versicolor activity of chlorophorin, however, was similar to the other extractives. Isoprenoid substitution has been reported to significantly increase stilbene fungal activity (Kindl 1985;Aguamah et al 1981), but our data suggest that the increased activity is limited to certain fungi. The mechanism by which stilbenes inhibit wood-decaying fungi is probably different for isoprenoid-vs. nonisoprenoid-s bstituted stilbenes, and thus our prior structure-activity relationship (SAR) results on the inactivity of 4 / -substituted stilbenes (Schultz et al 1990) are not applicable to this 4'-isoprenoid stilbene.…”
Section: Bioactivitiescontrasting
confidence: 70%
“…A 96 h time course per elicitor treatment was conducted including the following time points: 0, 0.5, 1, 3, 6,9,12,15,18,21,24,30,36,40,48,72 Extraction and Analyses of Stilbenoids from the Culture Medium. Stilbenoids were extracted from the medium of NaOAc-, H 2 O 2 -, and MeJA-treated hairy roots as described before.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…Recently, three stilbene phytoalexins were isolated in this laboratory from peanut kernels exposed to their native microflora; two of the compounds were novel and one had been previously described (Aguamah et a!., 1981). These compounds have been assigned the trivial names arachidin I, I1 and I11 (Fig.…”
Section: Oh -Ohmentioning
confidence: 99%
“…All three peanut phytoalexins inhibited both germination and hyphal extension of A.Jauus in the pg ml-I range. Since peanut kernels are capable of synthesizing these compounds in the low mg g-' range (Aguamah et al, 1981), an investigation was begun into why A.Javus colonizes peanut kernels. There were differences between variouscultivars in the initial rateofaccumulation of phytoalexins in response to slicing and these differences correlated with their dry seed resistance to colonization by A.Javus.…”
Section: Phytoalexin Accumulation In Peanut Kernels After Woundingmentioning
confidence: 99%