2019
DOI: 10.1016/j.phytol.2019.01.023
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Sesquiterpene and monoterpene derivatives from the soil-derived fungus Trichoderma reesei PSU-SPSF013

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Cited by 11 publications
(31 citation statements)
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“…Trichocitrinovirene A ( 1 ) was isolated as a colorless gum and had the molecular formula C 15 H 22 O 5 on the basis of the HRESIMS peak at m / z 305.1359 [M + Na] + . The IR spectrum exhibited absorption bands at 3336, 1684, and 1649 cm −1 for hydroxy, conjugated carboxyl carbonyl, and double bond functional groups, respectively [ 10 ]. The 1 H NMR spectrum ( Table 1 ) displayed characteristic signals for two olefinic protons of two trisubstituted alkenes (δ H 6.64, d, J = 10.5 Hz, and 5.31, s, each 1H), two methine protons (δ H 3.06 and 1.35, each m, 1H), one set of equivalent oxymethylene protons (δ H 3.92, s, 2H), three sets of nonequivalent methylene protons (δ H 3.40 and 3.30, each d, J = 16.8 Hz, 1H; δ H 2.13 and 2.04, each m, 1H; δ H 1.81 and 1.39, each m, 1H), and an isopropyl group (δ H 1.71, m, 1H, and δ H 0.95 and 0.82, each d, J = 6.9 Hz, 3H).…”
Section: Resultsmentioning
confidence: 99%
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“…Trichocitrinovirene A ( 1 ) was isolated as a colorless gum and had the molecular formula C 15 H 22 O 5 on the basis of the HRESIMS peak at m / z 305.1359 [M + Na] + . The IR spectrum exhibited absorption bands at 3336, 1684, and 1649 cm −1 for hydroxy, conjugated carboxyl carbonyl, and double bond functional groups, respectively [ 10 ]. The 1 H NMR spectrum ( Table 1 ) displayed characteristic signals for two olefinic protons of two trisubstituted alkenes (δ H 6.64, d, J = 10.5 Hz, and 5.31, s, each 1H), two methine protons (δ H 3.06 and 1.35, each m, 1H), one set of equivalent oxymethylene protons (δ H 3.92, s, 2H), three sets of nonequivalent methylene protons (δ H 3.40 and 3.30, each d, J = 16.8 Hz, 1H; δ H 2.13 and 2.04, each m, 1H; δ H 1.81 and 1.39, each m, 1H), and an isopropyl group (δ H 1.71, m, 1H, and δ H 0.95 and 0.82, each d, J = 6.9 Hz, 3H).…”
Section: Resultsmentioning
confidence: 99%
“…virens [ 11 12 ], T . reesei [ 10 ], and Xylaria sp. [ 8 , 13 ] whereas compound 7 was obtained from Fusidium sp.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, only 115 was active against C. neoformans ATCC90112 with the MIC value of 32 μg/mL. 55 Compounds 295 – 297 also displayed moderate inhibitory effects on MR Staphylococcus aureus, Staphylococcus aureus and Bacillus subtilis , which could be the major anti-bacterial constituents of Cephalotrichum microsporum . 104 Tolypocladin K 149 displayed moderate antifungal activity against Sclerotinia sclerotiorun, Helminthosporium maydis, Botrytis cinereal Pers.…”
Section: Biological Activity Of New Compounds Derived From Soil Fungimentioning
confidence: 99%
“… 38 Three new sesquiterpenes Trichodermapenes A-C 113 – 115 ( Figure 3A ) were isolated from the soil-derived fungus Trichoderma reesei PSU-SPSF013. 55 Chemical investigation of the Dictyosporium digitatum fungus resulted in the identification of three undescribed compounds 116 – 118 ( Figure 3A ). which were named Dictyosporin A 116 , Dictyosporin B 117 , Dictyosporin C 118 respectively.…”
Section: Structure Types Of New Compounds Derived From Soil Fungimentioning
confidence: 99%
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