Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Myint Myint, Khine"'
Autor:
Irina Smirnova, Anastasiya Petrova, Gul’nara Giniyatullina, Anna Smirnova, Alexandrina Volobueva, Julia Pavlyukova, Vladimir Zarubaev, Tran Van Loc, Thao Tran Thi Phoung, Vu Thi Bich Hau, Nguyen Thi Thu Thuy, Myint Myint Khine, Oxana Kazakova
Publikováno v:
Molecules, Vol 27, Iss 23, p 8499 (2022)
A series of sixteen A-ring modified (2,3-indolo-, 2-benzylidene) oleanonic acid derivatives, holding some cyclic amines, linear polyamines and benzylaminocarboxamides at C28, has been synthesized and screened for antiviral activity against influenza
Externí odkaz:
https://doaj.org/article/6674901da53d452e9626f48bb861e9b7
Autor:
Thant Zin Tun, null Nurlatifah, Aung Than Htwe, Ni Ni Than, Myint Myint Khine, Suchana Chavanich, Voranop Viyakarn, Atsuhiko Isobe, Haruhiko Nakata
Publikováno v:
Science of The Total Environment. 889:163983
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed0ad42648fab54080526b437abd18fe
https://doi.org/10.1016/j.scitotenv.2023.163983
https://doi.org/10.1016/j.scitotenv.2023.163983
Autor:
Petrova, Anastasiya V., Smirnova, Irina E., Fedij, Sergey V., Pavlyukova, Yulia N., Zarubaev, Vladimir V., Tran Thi Phuong, Thao, Myint Myint, Khine, Kazakova, Oxana B.
Publikováno v:
Molbank; Jun2023, Vol. 2023 Issue 2, pM1626, 5p
Autor:
Irina Smirnova, Anastasiya Petrova, Alexander Lobov, El’za Minnibaeva, Thao Tran Thi Phoung, Loc Tran Van, Myint Myint Khine, Iana Esaulkova, Alexander Slita, Vladimir Zarubaev, Oxana Kazakova
Publikováno v:
The Journal of antibiotics. 75(5)
A series of lupane-, oleanane- and dammarane-based triterpenoids with 3β-amino, A-ring azepano- and 3,4-seco-fragments has been synthesized and evaluated for antiviral activity against influenza A(H1N1) virus. It was found that azepanodipterocarpol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b030e2339d13fea975c7bc44ddc48a0d
https://pubmed.ncbi.nlm.nih.gov/35246615
https://pubmed.ncbi.nlm.nih.gov/35246615
Po-sa plant possesses many useful biological activities which have been the reason for the selection of this plant for the present paper. The present paper is concerned with detection of acute toxicity, antioxidant and cholesterol lowering activities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a3d74f1839d6aa70c7e4fd8a2aaa44
Autor:
Katrin Franke, Myint Myint Khine, Jürgen Schmidt, Norbert Arnold, Ludger A. Wessjohann, Andrea Porzel
Publikováno v:
Biochemical Systematics and Ecology. 35:517-524
A new cardenolide, 17β-H-periplogenin-3- O -β- d -digitoxoside ( 1 ), and a new pregnane glycoside, Δ 5 -pregnene-3β,16α-diol-d- O -[2,4- O -diacetyl-β-digitalopyranosyl-(1 → 4)-β- d -cymaropyranoside]-16- O -[β- d -glucopyranoside] ( 2 ) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b7789830c77980d5d750a344155f37
https://doi.org/10.1016/j.bse.2007.01.006
https://doi.org/10.1016/j.bse.2007.01.006
Autor:
Jürgen Schmidt, Ludger A. Wessjohann, Norbert Arnold, Katrin Franke, Myint Myint Khine, Andrea Porzel
Publikováno v:
Fitoterapia. 75:779-781
A new cardenolide, (17α)- H -periplogenin-3- O -β- d -glucopyranosyl-(1–4)-2- O -acetyl-3- O -methyl-β-fucopyranoside ( 1 ), was isolated from the roots of Streptocaulon tomentosum .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd75021e6ade545ecba07980913052f2
https://doi.org/10.1016/j.fitote.2004.06.007
https://doi.org/10.1016/j.fitote.2004.06.007
Autor:
Heinz H. Fiebig, Katrin Franke, Luay Rashan, Joachim Neumann, Myint Myint Khine, Gerhard Kelter, Ludger A. Wessjohann
Publikováno v:
Journal of ethnopharmacology. 134(3)
For identification of the active constituents we investigated the anticancer activity of cardenolides from Streptocaulon tomentosum WightArn. (Asclepiadaceae) and from Nerium oleander L. (Apocynaceae) which are both used against cancer in the traditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4dab4a1b6be56b37e6365a28c2af300
https://pubmed.ncbi.nlm.nih.gov/21291990
https://pubmed.ncbi.nlm.nih.gov/21291990