Likhitwitayawuid Kittisak, Sawasdee Kanokporn, Kirtikara Kanyawim
Department of Pharmacognosy, Faculty of Pharmaceutical Sciences Chulalongkorn University, Bangkok, Thailand.
Planta Med. 2002 Sep;68(9):841-3. doi: 10.1055/s-2002-34403.
Fom the stem wood of Dracaena loureiri, a new homoisoflavanone named loureiriol (1) and eight known flavonoid and stilbenoid derivatives, including 5,7-dihydroxy-3-(4-hydroxybenzyl)-4-chromanone (2), 4,4'-dihydroxy-2,6-dimethoxydihydrochalcone (3), 2,4'-dihydroxy-4,6-dimethoxydihydrochalcone (4), 4'-hydroxy-2,4,6-trimethoxydihydrochalcone (5), 4,6,4'-trihydroxy-2-methoxydihydrochalcone (6), 4,3',5'-trihydroxystilbene (7), 4,3'-dihydroxy-5'-methoxystilbene (8) and 4-hydroxy-3',5'-dimethoxystilbene (9) were isolated. These compounds were evaluated for their inhibitory activity against the enzymes cyclooxygenase-1 and cyclooxygenase-2. Potent but non-selective activity was found for the stilbenoids 7-9 (IC(50) 1.29 - 4.92 microM) whereas weak or no activity was observed for the flavonoids 1-6.
从海南龙血树的茎木中分离得到一种新的高异黄酮类化合物,命名为龙血树醇(1)以及8种已知的黄酮类和芪类衍生物,包括5,7-二羟基-3-(4-羟基苄基)-4-色满酮(2)、4,4'-二羟基-2,6-二甲氧基二氢查耳酮(3)、2,4'-二羟基-4,6-二甲氧基二氢查耳酮(4)、4'-羟基-2,4,6-三甲氧基二氢查耳酮(5)、4,6,4'-三羟基-2-甲氧基二氢查耳酮(6)、4,3',5'-三羟基芪(7)、4,3'-二羟基-5'-甲氧基芪(8)和4-羟基-3',5'-二甲氧基芪(9)。对这些化合物进行了环氧合酶-1和环氧合酶-2抑制活性的评估。发现芪类化合物7-9具有较强但非选择性的活性(IC(50) 1.29 - 4.92 microM),而黄酮类化合物1-6的活性较弱或无活性。