Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Araya Jatisatienr"'
Autor:
Pitchaya Mungkornasawakul, Stephen G. Pyne, Alison T. Ung, Araya Jatisatienr, Anthony C. Willis
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 8, Pp o1878-o1879 (2009)
Crystals of the title compound, C22H29NO5·C4H8O2, {[systematic name: (2R,3R,5R,5aS,6R,8aR,9S)-(5Z)-5-[3-butyltetrahydro-6-methyl-2,5-methano-4,3,8a-[1]propanyl[3]ylidenefuro[3,2-f][1,4]oxazepin-7(5H)-ylidene]-4-methoxy-3-methylfuran-2(5H)-one ethyl
Externí odkaz:
https://doaj.org/article/d2161c1e0e0244788866bc8eab73c410
Autor:
Kwankamol Sastraruji, Araya Jatisatienr, Stephen G. Pyne, Thanapat Sastraruji, Alison T. Ung, Renate Griffith
Publikováno v:
Tetrahedron. 68:7103-7115
Thirty-two new stemofoline analogues were prepared from didehydrostemofoline for studies as AChE inhibitors. C-3 Side-chain modified amino, carbamate, triazole and oxazole stemofoline derivatives were prepared. In general the amine derivatives were f
Publikováno v:
Biological Sciences Publications
Bulbuls (Passeriformes:Pycnonotidae) are a biodiverse group of birds that produce a variety of vocalisations, yet the vocal behaviour of most bulbuls has not been formally described or the subject of bioacoustical study. We present the first detailed
Publikováno v:
Asian Journal of Plant Sciences. 10:338-341
Autor:
Alison T. Ung, Sukanda Chaiyong, Araya Jatisatienr, Stephen G. Pyne, Wilford Lie, Thanapat Sastraruji
Publikováno v:
Journal of Natural Products. 74:60-64
A new stemofoline alkaloid, (2'S)-hydroxy-(11S,12R)-dihydrostemofoline (3), new stemofurans M-R (8-13), and known compounds stemofoline (1), (2'S)-hydroxystemofoline (2), stemofuran E (4), stemofuran F (5), stemofuran J (6), and stilbostemin F (7) ha
Autor:
Alison T. Ung, Araya Jatisatienr, Sukanda Chaiyong, Thitima Urathamakul, Wilford Lie, Thanapat Sastraruji, Stephen G. Pyne, Pitchaya Mungkornasawakul
Publikováno v:
Journal of Natural Products. 73:1833-1838
The isolation of two new Stemona alkaloids, 1-hydroxyprotostemonine and stemocurtisine N-oxide, and a new benzofuran, stemofuran L, from the root extracts of Stemona curtisii is reported. The major known alkaloids from this plant extract, stemocurtis
Autor:
Araya Jatisatienr, Thanapat Sastraruji, Alison T. Ung, Stephen G. Pyne, Wilford Lie, Morwenna C. Williams
Publikováno v:
Journal of Natural Products. 68:1763-1767
Six new stemofoline alkaloids, (2'R)-hydroxystemofoline (5), (3'R)-stemofolenol (6), (3'S)-stemofolenol (7), 1',2'-didehydrostemofoline-N-oxide (8), the first C(19) stemofoline alkaloid, methylstemofoline (9), and the first glycosidated Stemona alkal
Autor:
Xuan Duc Dau, Sonthaya Umsumarng, Araya Jatisatienr, Pornngarm Limtrakul, Kwankamol Sastraruji, Thanapat Sastraruji, Alison T. Ung, Sukanda Chaiyong, Pitchaya Mungkornasawakul, Stephen G. Pyne, Morwenna C. Baird, Rosdayati Alino Ramli
Publikováno v:
Natural Product Communications. 12:1934578X1701200
This report is an overview of our research on phytochemical, synthetic and biological studies of the Stemona and Stichoneuron species of plants.
Autor:
Alison T. Ung, Sonthaya Umsumarng, Araya Jatisatienr, Pornngarm Limtrakul, Thanapat Sastraruji, Pornsiri Pitchakarn, Stephen G. Pyne, Kwankamol Sastraruji, Komsak Pintha
Resistance to chemotherapy in cancer patients has been correlated to the overexpression of the ATPbinding cassette (ABC) drug transporters including P-glycoprotein (P-gp) that actively efflux chemotherapeutic drugs from cancer cells. We examined the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b89a14200cc948e714628d9c8f0bb2
https://hdl.handle.net/10453/27638
https://hdl.handle.net/10453/27638
Autor:
Allan H. White, Pitchaya Mungkornasawakul, Stephen G. Pyne, Brian W. Skelton, Alison T. Ung, Wilford Lie, Damrat Supyen, Chaiwat Jatisatienr, Araya Jatisatienr
Publikováno v:
Journal of Natural Products. 67:675-677
A new pentacyclic Stemona alkaloid, stemocurtisinol (3), with a pyrido[1,2-a]azepine A,B-ring system, and the known pyrrolo[1,2-a]azepine alkaloid oxyprotostemonine (4) have been isolated from a root extract of S. curtisii. The structure and relative