Ceramicines E—I, New Limonoids from Chisocheton ceramicus

スポンサーリンク

概要

• 論文の詳細を見る

• Five new limonoids, ceramicines E—I (1—5), have been isolated from the bark of Chisocheton ceramicus. The structures and relative stereochemistry of them were fully elucidated based on 1D- and 2D-NMR data. Ceramicines E—I (1—5) exhibited moderate cell growth inhibitory activities on a range of cell lines (HL-60, A549, MCF7, and HCT116). The absolute structure of previously isolated ceramicine B (6) was also elucidated by circular dichroism (CD) and X-ray analysis.

著者

• Hadi A.

  Department of Chemistry, Faculty of Science, University of Malaya

• Mohamad Khalit

  Department of Pharmacy, Faculty of Medicine, University of Malaya

• Morita Hiroshi

  Faculty of Pharmaceutical Sciences, Hoshi University

• Nugroho Alfarius

  Faculty of Pharmaceutical Sciences, Hoshi University

• Awang Khalijah

  Department Of Chemistry University Of Malaya

• Hirasawa Yusuke

  Faculty Of Pharmaceutical Sciences Hoshi University

• Shiro Motoo

  X-ray Research Laboratory Rigaku Cooperation

• Morita Hiroshi

  Faculty Of Environment Engineering The University Of Kitakyushu

• Wong Chin

  Faculty of Pharmaceutical Sciences, Hoshi University

• Shimada Misae

  Faculty of Pharmaceutical Sciences, Hoshi University

• Nagakura Yuta

  Faculty of Pharmaceutical Sciences, Hoshi University

• Kaneda Toshio

  Faculty of Pharmaceutical Sciences, Hoshi University

• Mohamad Khalit

  Department of Pharmacy, Faculty of Medicine, University Malaya

• Wong Chin

  Faculty of Pharmaceutical Science, Hoshi University

• Nugroho Alfarius

  Faculty of Pharmaceutical Science, Hoshi University

• Shiro Motoo

  X-Ray Research Laboratory, Rigaku Corporation

• Hirasawa Yusuke

  Faculty of Pharmaceutical Science, Hoshi University

関連論文

• Oppositinines A and B: New Vasorelaxant β-Carboline Alkaloids from Neisosperma oppositifolia
• Mononuclear to Tetranuclear Structural Transformation in Vanadyl Complexes of 3-Hydroxypyridine-2-carboxylic Acid (H_2hpic)
• Neolamarckines A and B, New Indole Alkaloids from Neolamarckia cadamba
• Relaxing effects of Phellinus gilvus extract and purified ebricoic acid on rat aortic rings
• Malycorins A-C, New Lycopodium Alkaloids from Lycopodium phlegmaria
• Alkaloids from the seeds of Peganum harmala showing antiplasmodial and vasorelaxant activities
• Studies on the constituents from the fruits of Phaleria macrocarpa
• Vasodilator Effect of Cassiarin A, a Novel Antiplasmodial Alkaloid from Cassia siamea, in Rat Isolated Mesenteric Artery
• X-ray Crystallography of D149 Ethyl Ester
• Molecular Design and Crystal Structures of Chiral Macrotricyclic Cage Amines
• The Synthesis, Molecular Structure and Selectivity of Macrotricyclic Ammonium-ion Receptor for Bromide Ion
• Ceramicines E—I, New Limonoids from Chisocheton ceramicus
• Pseuduvarines A and B, Two New Cytotoxic Dioxoaporphine Alkaloids from Pseuduvaria rugosa
• Delaumonones A and B, New Antiplasmodial Quassinoids from Laumoniera bruceadelpha
• Papuabalanols A and B, New Tannins from Balanophora papuana
• P-88 LCMS-GUIDED FRACTIONATION, A FAST WAY TO SEARCH NEW NATURAL PRODUCTS : ACYLPHENOLS AND QUINONES FROM MYRISTICA CRASSA
• Effects of Magnesium Sulfate on the Luminescence of Vibrio fischeri under Nutrient-Starved Conditions
• Effects of Magnesium Sulfate on the Luminescence of Vibrio fischeri under Nutrient-Starved Conditions
• Palmaenones A and B, Two New Antimicrobial Chlorinated Cyclopentenones from Discomycete Lachnum palmae
• Rupestines F-M, New Guaipyridine Sesquiterpene Alkaloids from Artemisia rupestris
• Antiplasmodial decarboxyportentol acetate and 3,4-dehydrotheaspirone from Laumoniera bruceadelpha
• Vasorelaxant effect of isoquinoline derivatives from two species of Popowia perakensis and Phaeanthus crassipetalus on rat aortic artery
• Cuspidans A and B, Two New Stilbenoids from the Bark of Gnetum cuspidatum
• New Tricyclic Alkaloids, Cassiarins G, H, J, and K from Leaves of Cassia siamea
• Sabiperones A-F, New Diterpenoids from Juniperus sabina
• Ceramicines J-L, new limonoids from Chisocheton ceramicus
• Indole Alkaloids from the Stem Bark of Ochrosia oppositifolia (Apocynaceae) with Antiplasmodial Activity
• Vasorelaxant activity of indole alkaloids from Tabernaemontana dichotoma
• Haworforbins A-C, new phenolics from Haworthia cymbiformis
• Vasorelaxant effect of FR900359 from Ardisia crenata on rat aortic artery
• Cyclic diarylheptanoids as inhibitors of NO production from Acer nikoense

もっと見る 閉じる

スポンサーリンク