Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nanang Rudianto Ariefta"'
Publikováno v:
Pharmaceutics, Vol 14, Iss 3, p 544 (2022)
The emerging spread of drug-resistant malaria parasites highlights the need for new antimalarial agents. This study evaluated the growth-inhibitory effects of sparsomycin (Sm), a peptidyl transferase inhibitor, against Plasmodium falciparum 3D7 (chlo
Externí odkaz:
https://doaj.org/article/d32521c238b04528874bcae910b09d26
Autor:
Makoto Fujita, Nanang Rudianto Ariefta, Takuya Koseki, Yoshimasa Taniguchi, Yoshihito Shiono, Muhlisun Azim, Takako Aboshi
Publikováno v:
Organic Letters. 22:3161-3165
3-(3-Hydroxy-2-(hydroxymethyl)phenyl)propanoic acid, 2-hydroxymethyl-3-hydroxy-(E)-cinnamic acid, and colletofurans A–E were isolated from Colletotrichum boninense AM-12–2. Colletofurans A–E are th...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc42a35c194648824e477d3a292f4e7e
https://doi.org/10.1021/acs.orglett.0c00925
https://doi.org/10.1021/acs.orglett.0c00925
Publikováno v:
South African Journal of Botany. 128:35-41
Phytochemical investigation led to the isolation of three alkaloids [skimmianine (1), vulcanine (2) and evoxine (3)] from the aerial parts of Haplophyllum tuberculatum, and two diacetylenic spiroketal enol ethers [spiroketalenolether polyyne (4) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c24b03a1183c5ec851810a86f0312b8
https://doi.org/10.1016/j.sajb.2019.10.005
https://doi.org/10.1016/j.sajb.2019.10.005
Autor:
Nanang Rudianto Ariefta, Ari Widiyantoro, Junpei Abe, Yoshihito Shiono, Tetsuya Murayama, Rikhsan Kurniatuhadi, Desi Harneti, Takuya Koseki, Abdul Malik, Naoaki Kurisawa, Suwardi Annas, Takuma Suzuki, Rani Maharani, Tomoki Nakamura, Unang Supratman, Takako Aboshi, Ken-ich Kimura
Publikováno v:
Phytochemistry Letters. 31:85-91
Fractionation of ethyl acetate extract obtained by culturing the endophytic fungus Pseudocosmospora sp. Bm-1-1 resulted in the isolation of four new meroterpenoids, cosmosporin A (1), 6-carboxy-cosmosporin A (2), rel-(6aS,10aR)-Δ9-tetrahydrocannabio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b23c3bb0012d065328a3b830a6d0ae97
https://doi.org/10.1016/j.phytol.2019.03.014
https://doi.org/10.1016/j.phytol.2019.03.014
Autor:
Ken-ichi Kimura, Yoshihito Shiono, Takuma Suzuki, Hiroyuki Momma, Hiroshi Furuno, Rani Maharani, Desi Harneti, Takuya Koseki, Eunsang Kwon, Nanang Rudianto Ariefta, Unang Supratman
Publikováno v:
Fitoterapia. 132:75-81
Five polyketides, paralactonic acids A-E (1-5) were isolated from Paraconiothyrium sp. SW-B-1, an endophytic fungus isolated from the seaweed, Chondrus ocellatus Holmes. Their structures were determined by various spectroscopic methods, predominantly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf2d396120857a0a47bc13210f91ab02
https://doi.org/10.1016/j.fitote.2018.11.017
https://doi.org/10.1016/j.fitote.2018.11.017
Autor:
Badgar Battsetseg, Banzragch Battur, Javzan Batkhuu, Orkhon Banzragchgarav, Punsantsogvoo Myagmarsuren, Yoshifumi Nishikawa, Nanang Rudianto Ariefta, Toshihiro Murata
Publikováno v:
Parasitology International. 85:102424
application/pdf
179 compounds in a Mongolian compound library were investigated for their inhibitory effect on the in vitro growth of Plasmodium falciparum and Toxoplasma gondii. Among these compounds, brachangobinan A at a half-maximal inhibiti
179 compounds in a Mongolian compound library were investigated for their inhibitory effect on the in vitro growth of Plasmodium falciparum and Toxoplasma gondii. Among these compounds, brachangobinan A at a half-maximal inhibiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3944e789d8da5532c058ba0f93ede062
https://doi.org/10.1016/j.parint.2021.102424
https://doi.org/10.1016/j.parint.2021.102424
Autor:
Abdou Tchoukoua, Jun Yoshida, Yoshiaki Ito, Mireille Heti Douanla, Yoshihito Shiono, Bonaventure T. Ngadjui, Nanang Rudianto Ariefta
Publikováno v:
Fitoterapia. 151:104859
Six new triterpenoid saponins, named senegalosides A–F (1–6) were isolated from the seedpods and roots of Acacia senegal (Mimosaceae). Their structures were elucidated using 1D and 2D-NMR spectroscopic analysis and mass spectrometry. Compound 1 p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70a71ade578dce90a7585e0ac422c87
https://doi.org/10.1016/j.fitote.2021.104859
https://doi.org/10.1016/j.fitote.2021.104859
Autor:
Takuma Suzuki, Keitaro Tawaraya, Tetsuya Murayama, Jun Yoshida, Shota Uesugi, Nanang Rudianto Ariefta, Ken-ichi Kimura, Narandulam Usukhbayar, Chairil Anwar, Handojo Hadi Nurjanto, Takuya Koseki, Takako Aboshi, Yoshihito Shiono, Niken Istikhari Muslihah
Publikováno v:
The Journal of Antibiotics. 70:1133-1137
The novel compound, 11-O-methylpetasitol (1), was isolated from Penicillium sp. N-175-1, and two new compounds, cosmochlorins D (5) and E (6), were isolated from Phomopsis sp. N-125. In addition, three known eremophilane sesquiterpenes, sporogen-AO1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e432fa217cf32987864b243db8ac868
https://doi.org/10.1038/ja.2017.125
https://doi.org/10.1038/ja.2017.125
Autor:
Takuya Koseki, Tetsuya Murayama, Handojo Hadi Nurjanto, Hiroshi Furuno, Nanang Rudianto Ariefta, Tatsuya Ashitani, Yoshihito Shiono, Ken-ichi Kimura, Keitaro Tawaraya, Narandulam Usukhbayar, Eunsang Kwon, Priska Kristiana, Hiroyuki Momma
Publikováno v:
Tetrahedron Letters. 58:4082-4086
Two sesquiterpene-epoxycyclohexenone conjugates, nectrianolins A ( 1 ) and B ( 2 ), together with a sesquiterpene, nectrianolin C ( 3 ), were isolated from the brown rice culture of Nectria pseudotrichia 120-1NP, an endophytic fungus isolated from Gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e47fcc0a12c75bdec756a592b42f5c44
https://doi.org/10.1016/j.tetlet.2017.09.032
https://doi.org/10.1016/j.tetlet.2017.09.032
Publikováno v:
Tetrahedron Letters. 64:152736
A pair of new diastereomeric isoindolinone alkaloids, spirocollequins A and B, were isolated from an endophytic fungus, Colletotrichum boninense AM-12-2. Their structures are featuring a 4,5-dihydro-spiro[furan-2,1′-isoindolin]-3′-one core. Their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b349970b5396ca92bbe82c3893f206c
https://doi.org/10.1016/j.tetlet.2020.152736
https://doi.org/10.1016/j.tetlet.2020.152736