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hyssopus_officinalis_l [2015/07/10 07:34] – andreas | hyssopus_officinalis_l [2017/11/21 21:30] (aktuell) – andreas |
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[[http://www.tropicos.org/Name/17600092?tab=subordinatetaxa]] | [[http://www.tropicos.org/Name/17600092?tab=subordinatetaxa]] |
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"The essential oils from different parts of hyssop (Hyssopus officinalis L.) were investigated by means of GC and GC-MS at three stages of development of the plant. Besides the main components [[http://pubchem.ncbi.nlm.nih.gov/compound/11038|pinocamphone]], camphor and β-pinene, 15 other terpenes were detected, among which were isopinocamphone, α and β-phellandrene, germacrene D, and some derivatives of myrtenol. The sesquiterpene alcohol hedycaryol was found to be converted to elemol during GC and MS analysis... Compared with the essential oil content (0.03–0.16% of the fresh plant material), the glycosidic bound volatiles were present in lower concentrations (0.01–0.06%). The glycosidic fraction was hydrolysed by means of Pectinol C and β-glucosidase yielding among others octan-3-ol, linalol, cis-nerolidol, benzyl alcohol, phenylethanol, eugenol and o-vanillin. The bicyclic terpenes myrtenol and verbenol could only be detected in small amounts as glycosides of the leaves. This fact gives reason for doubt about a direct connection between the glycosidic bound volatiles and the biogenesis of the essential oil components in hyssop." \\ | "The essential oils from different parts of hyssop (Hyssopus officinalis L.) were investigated by means of GC and GC-MS at three stages of development of the plant. Besides the main components [[http://pubchem.ncbi.nlm.nih.gov/compound/11038|pinocamphone]], camphor and β-pinene, 15 other terpenes were detected, among which were isopinocamphone, α and β-phellandrene, germacrene D, and some derivatives of myrtenol. The sesquiterpene alcohol hedycaryol was found to be converted to elemol during GC and MS analysis... Compared with the essential oil content (0.03-0.16% of the fresh plant material), the glycosidic bound volatiles were present in lower concentrations (0.01-0.06%). The glycosidic fraction was hydrolysed by means of Pectinol C and β-glucosidase yielding among others octan-3-ol, linalol, cis-nerolidol, benzyl alcohol, phenylethanol, eugenol and o-vanillin. The bicyclic terpenes myrtenol and verbenol could only be detected in small amounts as glycosides of the leaves. This fact gives reason for doubt about a direct connection between the glycosidic bound volatiles and the biogenesis of the essential oil components in hyssop." \\ |
[Essential oils and glycosidic bound volatiles from leaves, stems, flowers and roots of Hyssopus officinalis L.(Lamiaceae)., Schulz, G., Stahl‐Biskup, E., Flavour and fragrance journal, 6(1), 1991, 69-73] | [Essential oils and glycosidic bound volatiles from leaves, stems, flowers and roots of Hyssopus officinalis L.(Lamiaceae)., Schulz, G., Stahl‐Biskup, E., Flavour and fragrance journal, 6(1), 1991, 69-73] |
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{{:pinocamphone.jpg|}} pinocamphone {{:isopinocamphone.jpg|}} isopinocamphone \\ | |{{:pinocamphone.jpg|}} \\ pinocamphone | {{:isopinocamphone.jpg|}} \\ isopinocamphone | {{camphor.jpg| camphor}} \\ camphor | {{:beta_pinene.jpg| β-pinene }} \\ β-pinene | |
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"Pinocamphone and [[http://pubchem.ncbi.nlm.nih.gov/compound/6427105|isopinocamphone]] are present in H. officinalis (4.4% and 43.3%, respectively), according to the ISO 9841 Standard (1991 E) but they are lacking in var. decumbens, where linalool (51.7%), 1,8-cineole (12.3%) and limonene (5.1%) instead are predominant. The disc diffusion tests carried out on Gram-positive (Staphylococcus aureus and Enterococcus spp.) and Gram-negative bacteria (Klebsiella oxytoca, Escherichia coli, Proteus mirabilis, Pseudomonas spp. and two strains of Salmonella spp.) showed an antimicrobial activity generally negligible for H. officinalis, but broader, and in a few cases more evident (Enterococcus spp. and E. coli), for var. decumbens. All yeasts (seven strains of Candida albicans, C. krusei and C. tropicalis) were strongly inhibited by both species... Linalool, and in a lesser way, 1,8-cineole, may contribute to the greater antimicrobial activity of var. decumbens in comparison with H. officinalis, while limonene may be responsible for the antimycotic action observed in both oils, as suggested by results of the disc diffusion tests carried out on the pure reference substances." \\ | "Pinocamphone and [[http://pubchem.ncbi.nlm.nih.gov/compound/6427105|isopinocamphone]] are present in H. officinalis (4.4% and 43.3%, respectively), according to the ISO 9841 Standard (1991 E) but they are lacking in var. decumbens, where linalool (51.7%), 1,8-cineole (12.3%) and limonene (5.1%) instead are predominant. The disc diffusion tests carried out on Gram-positive (Staphylococcus aureus and Enterococcus spp.) and Gram-negative bacteria (Klebsiella oxytoca, Escherichia coli, Proteus mirabilis, Pseudomonas spp. and two strains of Salmonella spp.) showed an antimicrobial activity generally negligible for H. officinalis, but broader, and in a few cases more evident (Enterococcus spp. and E. coli), for var. decumbens. All yeasts (seven strains of Candida albicans, C. krusei and C. tropicalis) were strongly inhibited by both species... Linalool, and in a lesser way, 1,8-cineole, may contribute to the greater antimicrobial activity of var. decumbens in comparison with H. officinalis, while limonene may be responsible for the antimycotic action observed in both oils, as suggested by results of the disc diffusion tests carried out on the pure reference substances." \\ |
[Muscle relaxing activity of Hyssopus officinalis essential oil on isolated intestinal preparations., Lu, M., Battinelli, L., Daniele, C., Melchioni, C., Salvatore, G., Mazzanti, G., Planta medica, 68(3), 2002, 213-216] | [Muscle relaxing activity of Hyssopus officinalis essential oil on isolated intestinal preparations., Lu, M., Battinelli, L., Daniele, C., Melchioni, C., Salvatore, G., Mazzanti, G., Planta medica, 68(3), 2002, 213-216] |
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Herb (Hyssopi herba) and essential oil (Hyssopi aetheroleum) are traditionally used to treat respiratory ailments (cough, bronchial inflammation and nasal congestion). The oil is a gentle stimulant of circulation and also used in eyewashes and as a gargle... Expectorant properties are linked to marrubiin, while the antiseptic, spasmolytic and stimulant effects are ascribed to the essential oil. Pinocamphone and isopinocamphone are neurotoxic anf thus similar to thujone. They are thought to inhibit cell respiration, resulting in spasms and epileptic fits at toxic doses. the essential oil should not be taken internally except in dilute form." \\ | Herb (Hyssopi herba) and essential oil (Hyssopi aetheroleum) are traditionally used to treat respiratory ailments (cough, bronchial inflammation and nasal congestion). "The oil is a gentle stimulant of circulation and also used in eyewashes and as a gargle... Expectorant properties are linked to marrubiin, while the antiseptic, spasmolytic and stimulant effects are ascribed to the essential oil. Pinocamphone and isopinocamphone are neurotoxic and thus similar to thujone. They are thought to inhibit cell respiration, resulting in spasms and epileptic fits at toxic doses. The essential oil should not be taken internally except in dilute form." \\ |
[Medicinal Plants of the World. Ben-Erik Van Wyk and Michael Wink, Pretoria 2004, 177] | [Medicinal Plants of the World. Ben-Erik Van Wyk and Michael Wink, Pretoria 2004, 177] |
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[Isolation of α-glusosidase inhibitors from hyssop (Hyssopus officinalis)., Matsuura, H., Miyazaki, H., Asakawa, C., Amano, M., Yoshihara, T., Mizutani, J., Phytochemistry, 65(1), 2004, 91-97] | [Isolation of α-glusosidase inhibitors from hyssop (Hyssopus officinalis)., Matsuura, H., Miyazaki, H., Asakawa, C., Amano, M., Yoshihara, T., Mizutani, J., Phytochemistry, 65(1), 2004, 91-97] |
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Main components of Iranian supercritical fluid extracts were sabinene (4.2–17.1%), iso-pinocamphene (0.9–16.5%) and pinocamphene (0.7–13.6%). \\ | Main components of Iranian supercritical fluid extracts were sabinene (4.2-17.1%), iso-pinocamphene (0.9-16.5%) and pinocamphene (0.7-13.6%). \\ |
[Supercriticial fluid extraction of flavors and fragrances from Hyssopus officinalis L. cultivated in Iran., Kazazi, H., Rezaei, K., Ghotb-Sharif, S.J., Emam-Djomeh, Z., Yamini, Y., Food Chemistry, 105(2), 2007, 805-811] | [Supercriticial fluid extraction of flavors and fragrances from Hyssopus officinalis L. cultivated in Iran., Kazazi, H., Rezaei, K., Ghotb-Sharif, S.J., Emam-Djomeh, Z., Yamini, Y., Food Chemistry, 105(2), 2007, 805-811] |
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{{:hyssopus_officinalis_f.jpg?500}} \\ | {{:hyssopus_officinalis_f.jpg?600}} \\ |
Fuchs,L., New Kreüterbuch, t.483 (1543) \\ | Fuchs,L., New Kreüterbuch, t.483 (1543) \\ |
[[http://plantgenera.org/species.php?id_species=548155]] | [[http://plantgenera.org/species.php?id_species=548155]] |
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| {{http://www.botanische-spaziergaenge.at/Bilder/Lumix_4/P1220101.JPG}} \\ |
| Hyssopus officinalis \\ © Rolf Marschner (2009), |
| [[http://www.botanische-spaziergaenge.at/viewtopic.php?f=95&t=2110| www.botanische-spaziergaenge.at]] |