Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Macki Kaloga"'
Publikováno v:
Phytochemistry. 62:1257-1263
Separation of the methanolic seed extract of Ipomoea obscura afforded five indole alkaloids, three of them (ipobscurines B-D) being new natural products of a unique structural type characterized as serotonin hydroxycinnamic acid amide-type conjugates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28bb6b18e672c2cb764eb9e1502ab334
https://doi.org/10.1016/s0031-9422(02)00756-2
https://doi.org/10.1016/s0031-9422(02)00756-2
Publikováno v:
Phytochemistry. 51:1177-1180
N -Formylloline was isolated from roots of Argyreia mollis . This is the first identification of a 1-aminopyrrolizidine alkaloid (loline alkaloid) in a species of the Convolvulaceae. Lolines are only known from the genus Adenocarpus (Fabaceae) and ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f90c4732ff6cc09d32603d147f931ee
https://doi.org/10.1016/s0031-9422(99)00121-1
https://doi.org/10.1016/s0031-9422(99)00121-1
Publikováno v:
Phytochemistry. 50:267-271
A novel flavonoid, quercetin 7-methyl ether-3,3′-disulfate ( 5 ), was obtained from the roots of Argyreia mollis , together with the known compounds quercetin 7-methyl ether-3-sulfate ( 4 ) and kaempferol 7-methyl ether-3-sulfate ( 2 ). Two further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7dd82dcf29466f655f72f9cf0754216
https://doi.org/10.1016/s0031-9422(98)00502-0
https://doi.org/10.1016/s0031-9422(98)00502-0
Autor:
Thomas Hartmann, Karsten Siems, Macki Kaloga, Mahabir P. Gupta, Thomas Schimming, Eckart Eich, Ludger Witte, Kristina Jenett-Siems
Publikováno v:
Phytochemistry. 47:1551-1560
The common necine base of the novel pyrrolizidine alkaloids (ipangulines) isolated recently from Ipomoea hederifolia is not turneforcidine but its 1β-epimer, platynecine. Three novel ipangulines were isolated from the aerial parts of I. hederifolia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6306e3aeabfaede3824f6e4fde6cc00b
https://doi.org/10.1016/s0031-9422(97)01082-0
https://doi.org/10.1016/s0031-9422(97)01082-0
Publikováno v:
Planta Medica. 63:343-346
Four major cardenolide glycosides of Xysmalobium undulatum (L.) R. Br. roots (Uzara) have been isolated for the first time in pure form. The structures were elucidated by spectral analyses and determined as sophorosides and their 17-epimers, respecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd78df4f7403f7d2ef3b9784be2ae174
https://doi.org/10.1055/s-2006-957697
https://doi.org/10.1055/s-2006-957697
Autor:
M. R. Fesen, Macki Kaloga, A. Mazumder, Heinz H. Pertz, Yves Pommier, Eckart Eich, Jutta Schulz
Publikováno v:
Journal of Medicinal Chemistry. 39:86-95
The natural dibenzylbutyrolactone type lignanolide (-)-arctigenin (2), an inhibitor of human immunodeficiency virus type-1 (HIV-1) replication in infected human cell systems, was found to suppress the integration of proviral DNA into the cellular DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2558256c1b60f88701a3e402b9a8e75f
https://doi.org/10.1021/jm950387u
https://doi.org/10.1021/jm950387u
Publikováno v:
Phytochemistry. 37:1637-1640
Two new lignanamides were isolated from fruits of Jacquemontia paniculata var. paniculata . It could be shown that these compounds represent a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e227a20a4029ca13b97f40b0fc8f0f7e
https://doi.org/10.1016/s0031-9422(00)89582-5
https://doi.org/10.1016/s0031-9422(00)89582-5
Publikováno v:
Phytochemistry. 34:437-440
Four novel pyrrolizidine alkaloids were isolated from Ipomoea hederifolia. It could be shown by spectroscopic methods that the compounds represent two pairs of isomeric turneforcidine diesters with either erythro- or threo-2,3-dihydroxy-2-methyl-buty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2db54a7fce5550a5267f0c01059690ef
https://doi.org/10.1016/0031-9422(93)80025-n
https://doi.org/10.1016/0031-9422(93)80025-n
Autor:
Macki Kaloga, M. R. Fesen, A. Mazumder, Yves Pommier, Heinz H. Pertz, Jutta Schulz, Eckart Eich
Publikováno v:
ChemInform. 27
The natural dibenzylbutyrolactone type lignanolide (−)-arctigenin (2), an inhibitor of human immunodeficiency virus type-1 (HIV-1) replication in infected human cell systems, was found to suppress the integration of proviral DNA into the cellular D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0103973f3b8da623da013c083cc6b451
https://doi.org/10.1002/chin.199618235
https://doi.org/10.1002/chin.199618235
Autor:
Kristina Jenett-Siems, Eckart Eich, Petra Mann, Karsten Siems, Ludger Witte, Macki Kaloga, Jasmin Jakupovic
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74f5cdf79b74f25a41461369a55d456c
https://doi.org/10.1002/chin.199911251
https://doi.org/10.1002/chin.199911251