2015
DOI: 10.1016/j.phytochem.2015.06.012
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Chemical constituents of Abies fabri

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Cited by 26 publications
(15 citation statements)
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“…149 Juniperigiside (406) was reported from the CHCl 3 soluble fraction of the methanol extract of stem and leaves of the medicinal plant Juniperus rigida (Cupressaceae) 150 while compound 407 was obtained from Abies fabri (Pinaceae). 151 The dihydrobenzofuranoid neolignan bearing a 1,3,4,5-tetrasubstituted benzene ring ococymosin (408) was characterized from the stem or bark of the Madagascan plant Ocotea cymosa (Lauraceae). 152 It exhibited antiparasitic activity against the Dd2 strain of Plasmodium falciparum with an IC 50 of 0.45 mM.…”
Section: Benzofuransmentioning
confidence: 99%
“…149 Juniperigiside (406) was reported from the CHCl 3 soluble fraction of the methanol extract of stem and leaves of the medicinal plant Juniperus rigida (Cupressaceae) 150 while compound 407 was obtained from Abies fabri (Pinaceae). 151 The dihydrobenzofuranoid neolignan bearing a 1,3,4,5-tetrasubstituted benzene ring ococymosin (408) was characterized from the stem or bark of the Madagascan plant Ocotea cymosa (Lauraceae). 152 It exhibited antiparasitic activity against the Dd2 strain of Plasmodium falciparum with an IC 50 of 0.45 mM.…”
Section: Benzofuransmentioning
confidence: 99%
“…The absolute configuration of C-17 and C-23 has an important bearing on chemical shifts of C-20, C-22, and C-24 due to the anisotropic effect of the lactone oxygen atom. The 13 C NMR chemical shifts of C-20, C-22, and C-24 for (17 S ,23 S )-isomer were almost equal, however, those of (17 S ,23 R ), (17 R ,23 S ), and (17 R ,23 R )-isomers showed dramatical differences larger than 5 ppm [ 12 , 13 ]. Therefore, the absolute configurations of C-17 and C-23 for 1 were highly close to that of (17 S ,23 S )-isomer reported in the literature [ 12 ], and both determined to be S -configuration based on comparison of NMR spectroscopic data (C-20 ( δ C 43.4), C-22 ( δ C 44.6), and C-24 ( δ C 44.9)) with those of similar structures.…”
Section: Resultsmentioning
confidence: 99%
“…The 13 C NMR chemical shifts of C-20, C-22, and C-24 for (17 S ,23 S )-isomer were almost equal, however, those of (17 S ,23 R ), (17 R ,23 S ), and (17 R ,23 R )-isomers showed dramatical differences larger than 5 ppm [ 12 , 13 ]. Therefore, the absolute configurations of C-17 and C-23 for 1 were highly close to that of (17 S ,23 S )-isomer reported in the literature [ 12 ], and both determined to be S -configuration based on comparison of NMR spectroscopic data (C-20 ( δ C 43.4), C-22 ( δ C 44.6), and C-24 ( δ C 44.9)) with those of similar structures. The Me-21 and Me-27 were assigned as α - and β -orientation, respectively, based on the ROESY correlations of H-18 ( δ H 1.15) with H-20 ( δ H 2.14), H-24 α ( δ H 2.36) with H-21 ( δ H 0.91) and H-25 ( δ H 3.02), and H-24 β ( δ H 1.96) with H-27 ( δ H 1.23).…”
Section: Resultsmentioning
confidence: 99%
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“…Therefore, the use of medicinal plants implies a promising perspective for the treatment of MC. When determining the chemical composition and structure of active substances of medicinal plants and their medications by using modern high-precision methods (Makarova et al, 2013;Yong-Li et al, 2015), it was established that the essential oils of plants include various chemicals, for example, thymol, foams, and cineoles. A large number of terpenoids and terpenes provide oils with geroprotective properties and promote the regeneration of tissues (Kudryavtseva et al, 2016;Wenming et al, 2016).…”
Section: Introductionmentioning
confidence: 99%