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- Publications
- Influence
A new α-pyrone metabolite from a mangrove plant endophytic fungus, Fusarium sp.
- Y. Shiono, F. Shibuya, +4 authors K. Kimura
- Biology, Medicine
- Journal of Asian natural products research
- 3 April 2015
A new α-pyrone derivative, compound 2, and a known one, cladobotrin V, were isolated from the culture broth of the mangrove endophyte Fusarium sp. IM-37. Their structures were determined… Expand
A phytotoxic bicyclic lactone and other compounds from endophyte Xylaria curta
- Abdou Tchoukoua, Takuma Ota, +5 authors Y. Shiono
- Biology, Medicine
- Natural product research
- 9 January 2017
Abstract A new compound, (3aS,6aR)-4,5-dimethyl-3,3a,6,6a-tetrahydro-2H-cyclopenta [b]furan-2-one (2), along with two known metabolites, myrotheciumone A (1) and 4-oxo-4H-pyron-3-acetic acid (3) was… Expand
New naphthoquinone derivatives from Fusarium napiforme of a mangrove plant.
- U. Supratman, Nami Hirai, +7 authors Y. Shiono
- Chemistry, Medicine
- Natural product research
- 12 August 2019
Two new naphthoquinone derivatives, 6-hydroxy-astropaquinone B (1) and astropaquinone D (2) as well as the known compound 3-O-methyl-9-O-methylfusarubin (3) were isolated from Fusarium napiforme, an… Expand
New metabolites produced by endophyte Clonostachys rosea B5 - 2.
- U. Supratman, Takuma Suzuki, +7 authors Y. Shiono
- Biology, Medicine
- Natural product research
- 27 August 2019
The endophytic fungus, Clonostachys rosea B5-2 was isolated from mangrove plants and subjected to the one strain many compounds (OSMAC) methodology. By this approach, it was found that modification… Expand
(S)-2-Methyl-2-(4-methylpent-3-enyl)-6-(propan-2-ylidene)- 3,4,6,7-tetrahydropyrano(4,3-g)chromen-9(2H)-one
- Yasmiwar Susilawati, Ricky Nugraha, A. Muhtadi, Supriyatna Soetardjo, U. Supratman
- Chemistry
- 21 April 2015
A novel chromene, (S)-2-methyl-2-(4-methylpent-3-enyl)-6-(propan-2-ylidene)-3,4,6,7-tetrahydropyrano[4,3-g]chromen-9(2H)-one (1), was isolated from the leaves of Peperomia pellucida (Piperaceae). The… Expand
IDENTIFIKASI ANTOSIANIN BUAH DUWET (Syzygium cumini) MENGGUNAKAN KROMATOGRAFI CAIR KINERJA TINGGI - DIODE ARRAY DETECTION [Identification of Anthocyanins in Jambolan Fruit (Syzygium cumini) by High…
- P. Sari, C. Wijaya, D. Sajuthi, U. Supratman
- Chemistry, Physics
- 12 December 2009
The aim of this study was to determine the content of total monomeric anthocyanins and to identify the anthocyanin composition of jambolan fruit (Syzygium cumini) growing in Indonesia. Anthocyanins… Expand
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Cycloart-24-ene-26-ol-3-one, a New Cycloartane Isolated from Leaves of Aglaia exima Triggers Tumour Necrosis Factor-Receptor 1-Mediated Caspase-Dependent Apoptosis in Colon Cancer Cell Line
- Kok Hoong Leong, C. Looi, +5 authors K. Awang
- Biology, Medicine
- PloS one
- 12 April 2016
Plants in the Meliaceae family are known to possess interesting biological activities, such as antimalaral, antihypertensive and antitumour activities. Previously, our group reported the… Expand
Cytotoxic constituents from the bark of Aglaia eximia (Meliaceae)
- D. Harneti, A. Supriadin, +4 authors H. Hayashi
- Chemistry
- 1 May 2014
Abstract The new stigmastane steroid, 3,4-epoxy-(22R,25)-tetrahydrofuran-stigmast-5-en (1), along with two known triterpenoids (2–3) and two known steroids (4–5) were isolated from the stem bark of… Expand
Antifeedant Triterpenoids from the Seeds and Bark of Lansium domesticum cv Kokossan (Meliaceae)
- Tri Mayanti, R. Tjokronegoro, U. Supratman, M. R. Mukhtar, K. Awang, A. A. Hadi
- Biology, Medicine
- Molecules
- 29 March 2011
Two tetranortriterpenoids, kokosanolide A (1) and C (2) were isolated from the seeds and three onoceranoid-type triterpenoids: kokosanolide B (3), 8,14-secogammacera-7,14-diene-3,21-dione (4) and a… Expand
Cytotoxic Steroids from the Bark of Aglaia argentea (Meliaceae)
- Kindi Farabi, D. Harneti, +5 authors Y. Shiono
- Chemistry
- 1 October 2017
The study aimed to find a potential anticancer agent by isolating and identifying the chemical structure of compounds from Aglaia argentea and testing their cytotoxic effects against P-388 murine… Expand