Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Shorea uliginosa"'
Autor:
Ida Sufaidah, Istomo Istomo
Publikováno v:
Journal of Tropical Silviculture. 11:56-64
Ramin is one of slow growing spesies, have a medium until big measurement, have a silindris stem, high total reach 40-50 m with DBH reach 120 cm. The purpose of this research is to know association between ramin (Gonystylus bancanus (Miq.) Kurz) and
Autor:
Gusti Hardiansyah, Yeni Mariani, Denni Nurdwiansyah, Aripin Aripin, Fathul Yusro, Erianto Erianto, Hendarto Hendarto
Publikováno v:
Jurnal Biologi Tropis. 20:245-255
Non-forest estate (APL) such as Tawang Serimbak need to be maintained because they store various flora that is useful for human life, one of which is medicinal plants. The research objective is to identify, analyze the potential, and to know the prot
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Publikováno v:
Phytochemistry Letters. 32:123-128
In this study, the acetone-soluble parts of the stem bark of Shorea uliginosa were analyzed and three new resveratrol trimers, that is, uliginosides E–G (1–3), were isolated. The structures of these isolates were established on the basis of spect
Publikováno v:
Phytochemistry Letters. 28:1-7
A new resveratrol dimer C-glucoside [uliginosides D (1)] was isolated from the stem bark of Shorea uliginosa, along with 21 resveratrol derivatives (2–22). Eight of these compounds (1, 3–9) comprised the building block, 4-C-glucosylresveratrol (1
Publikováno v:
Trees. 29:527-537
This study shows that two emergent tree species growing in a nutrient-limited tropical peat swamp forest use different mechanisms for nutrient regulation. The main aim of this study is to understand the contribution of litterfall to nutrient supply a
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Autor:
Munekazu Iinuma, Yoshikazu Takahashi, Masayoshi Oyama, Ryuichi Sawa, Hironao Sajiki, Tetsuro Ito
Publikováno v:
Tetrahedron. 68:2950-2960
A rotational isomeric shoreaketone (1), identified as a skeletal member of resveratrol tetramers, was isolated from three species of Dipterocarpaceaeous plants: Shorea uliginosa, Shorea hemsleyana, and Vateria indica. The structure was elucidated by
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Publikováno v:
Tetrahedron Letters. 50:2516-2520
Two C-glucosides of resveratrol dimers (uliginoside A (1) and hemsleyanoloside B (2)) consisting of enantiomeric aglycones and two C-glucosides of resveratrol trimers (uliginosides B (3) and C (4)) consisting of diastereomeric aglycones were isolated