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See detailTriterpenoid saponins from the stem bark of pentaclethra eetveldeana
Pertuit, D.; Kapundu, M.; Mitaine-Offer, A.-C. et al

in Natural Product Communications (2019), 14(7),

Two previously undescribed triterpenoid saponins together with 4 known ones were isolated from the stem bark of Pentaclethra eetveldeana De Wild. & Th. Dur. Their structures were elucidated by ... [more ▼]

Two previously undescribed triterpenoid saponins together with 4 known ones were isolated from the stem bark of Pentaclethra eetveldeana De Wild. & Th. Dur. Their structures were elucidated by spectroscopic methods including 1D and 2D NMR experiments in combination with mass spectrometry as 3- O-β- d -glucopyranosyl- (1→2)- [β- d -glucopyranosyl- (1→3)]-β- d -glucopyranosyl- (1→4)- β- d -glucopyranosyl- (1→3)-α- l -rhamnopyranosyl- (1→2)-[β- d-glucopyranosyl- (1→4)]-α- l -arabinopyranosyloleanolic acid and 3- O -β- d -glucopyranosyl- (1→2)-[β- d -glucopyranosyl- (1→3)]-β- d -glucopyranosyl- (1→4)-β- d -glucopyranosyl- (1→3)- α -l -rhamnopyranosyl- (1→2)-[β- d -glucopyranosyl- (1→4)]-α- l -arabinopyranosylhederagenin. © The Author(s) 2019. [less ▲]

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See detailTriterpenoid saponins from the root bark of haplocoelum congolanum
Pertuit, D.; Mitaine-Offer, A.-C.; Miyamoto, T. et al

in Natural Product Communications (2019), 14(5),

Two undescribed triterpenoid saponins together with 5 known ones were isolated from the root bark of Haplocoelum congolanum Hauman. Their structures were elucidated by spectroscopic methods including one ... [more ▼]

Two undescribed triterpenoid saponins together with 5 known ones were isolated from the root bark of Haplocoelum congolanum Hauman. Their structures were elucidated by spectroscopic methods including one-dimensional and two-dimensional nuclear magnetic resonance experiments in combination with mass spectrometry as 3-O-(4-O-[3-hydroxy-3-methylglutaryl])-α-l-arabinopyranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl-(1→4)]-α-l-arabinopyranosyloleanolic acid and 3-O-α-l-arabinofuranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl-(1→4)]-α-l-arabinopyranosyloleanolic acid. © The Author(s) 2019 [less ▲]

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See detailChemical Composition and Acaricidal Activity of Thymus algeriensis Essential Oil against Varroa destructor
Kouache, Benmoussa; Brada, Moussa; Saadi, Abdelkader et al

in Natural Product Communications (2017), 12(0), 1-4

The aim of the present study was to determine the chemical composition and evaluate the acaricidal activity of Thymus algeriensis essential oil (TAEO) against Varroa destructor. This ectoparasitic mite is ... [more ▼]

The aim of the present study was to determine the chemical composition and evaluate the acaricidal activity of Thymus algeriensis essential oil (TAEO) against Varroa destructor. This ectoparasitic mite is a pest of the honey bee Apis mellifera. The essential oil from the aerial parts of T. algeriensis, obtained by hydrodistillation, was obtained in a yield of 2.8± 0.2%, w/w. The TAEO was analyzed by GC and GC/MS. Thirty-four compounds were identified, representing 99.3% of the oil. The main constituents were carvacrol (48.4%), γ-terpinene (14.9%), p-cymene (14.7%), and thymol (5.6%). Four lots were constituted at the level of an apiary in order to study the dynamics of the Varroa destructor and its host, Apis mellifera. After diagnosis by the biological method "install of diapers", the lots were treated at different doses of TAEO (0.1, 0.3 and 0.5%). TAEO was sprayed on top of the hives. The results show that TAEO at 0.5% resulted in a decrease in the rate of infestation of Varroa destructor, causing a mortality rate of 32.6% without negative effect on the nesting of the queen. The essential oil of T. algeriensis could be used as a bioacaricidal agent. [less ▲]

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See detailChemical Characterization of Essential Oils of Mints from Senegal
Diop, Serigne Mbacké; Guèye, Momar Talla; Ndiaye, Ibrahima et al

in Natural Product Communications (2016), 11(0), 1-2

Mints from Senegal were extracted separately from fresh (F) and shade-dried (D) plants by steam distillation. Yields were of 0.28 and 0.21% for M. citrata L., 0.21 and 0.18% for M. x piperita L. and 0.10 ... [more ▼]

Mints from Senegal were extracted separately from fresh (F) and shade-dried (D) plants by steam distillation. Yields were of 0.28 and 0.21% for M. citrata L., 0.21 and 0.18% for M. x piperita L. and 0.10 and 0.19% for M. spicata L. in the fresh and dried plants, respectively. GC/FID and GC/MS analysis revealed that many of the major compounds of essential oils decreased with drying. The prominent components of M. citrata oils were linalool that constituted 45.8% (F) and 42.0% (D) and linalyl acetate 42.7 (F) and 38.5% (D). Mentha x piperita was characterized by menthofuran with 30.7% (F) and 28.1% (D), menthol 15.9(F) and 16.4% (D), menthone 13.0 (F) and 14.2% (D), pulegone 17.6%(F) and 13.8%(D) and 1.8-cineole 3.7%(F) and 3.4% (D). Mentha spicata contained mainly carvone 67.8 and 74.7% and limonene 18.1 and 12.5% in the fresh and dried plants respectively. [less ▲]

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See detailTwo new aromadendrane sesquiterpenes from the stem bark of Alafia multiflora
Tchinda Tiabou, Alembert ULiege; Tsala, David E.; Nnanga, Nga et al

in Natural Product Communications (2014), 9(12), 1673-1675

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See detailArdisikivuoside, a new triterpenoid saponin from Ardisia kivuensis (Mysinaceae)
Ndontsa, Blanche; Tchinda Tiabou, Alembert ULiege; Teponno, Rémy et al

in Natural Product Communications (2012), 7

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See detailChemical Composition, Insecticidal Effect and Repellent Activity of Essential Oils of Three Aromatic Plants, Alone and in Combination, towards Sitophilus Oryzae L. (Coleoptera : Curculionidae)
Ngassoum, Martin B.; Ngamo Tinkeu, Léonard S.; Ngatanko, Iliassa et al

in Natural Product Communications (2007), 2(12), 1229-1232

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See detailN1,N2,N3-trisisopentenyl guanidine and N1,N2-diisopentenyl guanidine, two cytotoxic alkaloids from Alchornea cordifolia (Schumach.& Thonn.) Mull. Arg. (Euphorbiaceae) root barks.
Mavar-Manga, H.; Chapon, David; Hoet, Sara et al

in Natural Product Communications (2006), 1(12), 1097-1100

Detailed reference viewed: 85 (3 ULiège)