Zobrazeno 1 - 10
of 78
pro vyhledávání: '"E, Kemertelidze"'
Publikováno v:
Molecules, Vol 10, Iss 9, Pp 1135-1144 (2005)
Two high-molecular water-soluble preparations with high anticomplementary, antioxidant, antilipoperoxidant and antiinflammatory activities were isolated from the roots of Symphytum asperum and S. caucasicum. Their main chemical constituent was found
Externí odkaz:
https://doaj.org/article/fbc8e2a2e65647aab99ebb2632f3fef6
Autor:
Silvester Ponist, Lia Tsiklauri, L Slovák, Karol Svik, E Kemertelidze, Frantisek Drafi, Z Kemoklidze, M Chrastina, Katarína Bauerová
Publikováno v:
Physiological Research. :S75-S85
In this study, two extracts from Fatsia japonica-Fatsiphloginum™ (extract of triterpene glycosides containing 45-50 % of fatsiosides (FS)) and purified triterpene-rich extract of saponins with code name PS-551 (PS) were administered in combination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10ca05790e49537398121ebc5926b3c
https://doi.org/10.33549/physiolres.934328
https://doi.org/10.33549/physiolres.934328
Publikováno v:
Clinical and Experimental Pharmacology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0feb3b51054326460fba77718a2f861
https://doi.org/10.4172/2161-1459.c1.014
https://doi.org/10.4172/2161-1459.c1.014
Publikováno v:
Chemistry of Natural Compounds. 41:48-51
Five triterpenoid saponins were isolated from the stems of Hedera colchica K. Koch (Araliaceae). Two of them are new natural substances. HCS-A (1): 3-O-α-L-arabinopyranoside, 28-O-α-L-rhamnopyranosyl-(1→ 4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::051cd384e166c0e11d0ffd1fdeabf918
https://doi.org/10.1007/s10600-005-0072-4
https://doi.org/10.1007/s10600-005-0072-4
Publikováno v:
Phytotherapy Research. 19:158-161
The antifungal activity of a crude steroidal glycoside extract from Yucca gloriosa flowers, named alexin, was investigated in vitro against a panel of human pathogenic fungi, yeasts as well as dermatophytes and filamentous species. The minimal inhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a9dbb63bdcd2853e6608e81f50300f
https://doi.org/10.1002/ptr.1644
https://doi.org/10.1002/ptr.1644
Autor:
Guy Balansard, P. Timon-David, E. Kemertelidze, Vakhtang Mshvildadze, C. Di Giorgio, O. Ridoux, G. E. Dekanosidze, R. Elias, F. Delmas
Publikováno v:
Phytotherapy Research. 15:298-301
The in vitro antileishmanial activity of three saponins isolated from ivy, alpha-hederin, beta-hederin and hederacolchiside A(1), was investigated on parasites of the species Leishmania mexicana, in their promastigote and amastigote forms compared wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03fca8cb83b37eb45ee1ee1e39c3eb58
https://doi.org/10.1002/ptr.723
https://doi.org/10.1002/ptr.723
Autor:
E. Kemertelidze, Vakhtang Mshvildadze, Monique Gasquet, Riad Elias, P. Timon-David, F. Delmas, Nadine Azas, G. E. Dekanosidze, C. Di Giorgio
Publikováno v:
Planta Medica. 66:343-347
The in vitro antileishmanial activity of three saponins isolated from ivy, alpha-hederin, beta-hederin and hederacolchiside A1, was investigated on Leishmania infantum. The assessment of possible targets (membrane integrity, membrane potential, DNA s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d00356904fe6ae2559db6683dd7da1d
https://doi.org/10.1055/s-2000-8541
https://doi.org/10.1055/s-2000-8541
Publikováno v:
Planta Medica. 78
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50e1d9a545bea18f156e1af477a855e0
https://doi.org/10.1055/s-0032-1320245
https://doi.org/10.1055/s-0032-1320245
Publikováno v:
Georgian medical news. (203)
A chemical investigation of plant Satureja hortensis L. - garden savory (GS) has been carried out. It is established that the GS is rich in phenolic compounds. Flavonoids apigenin, luteolin, cinaroside, luteolin-glucuronide, luteolin-rutinoside, isor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::27d5cda89c44818b44834351d93a7223
https://pubmed.ncbi.nlm.nih.gov/22466541
https://pubmed.ncbi.nlm.nih.gov/22466541
Publikováno v:
Annals of the New York Academy of Sciences. 685:383-387
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8634b6d29bde3e5cb8f033fb9123dfca
https://doi.org/10.1111/j.1749-6632.1993.tb35894.x
https://doi.org/10.1111/j.1749-6632.1993.tb35894.x