Giang Phan Minh, Jin Hui Zi, Son Phan Tong, Lee Jeong Hyung, Hong Young Soo, Lee Jung Joon
Anticancer Research Laboratory, Korea Research Institute of Bioscience and Biotechnology, P.O. Box115, Yuseong, Daejeon 305-600, Korea.
J Nat Prod. 2003 Sep;66(9):1217-20. doi: 10.1021/np030139y.
Four ent-kaurane diterpenoids including two known, ent-7alpha,14beta-dihydroxykaur-16-en-15-one (1) and ent-18-acetoxy-7alpha-hydroxykaur-16-en-5-one (2), and two new, ent-1beta-acetoxy-7alpha,14beta-dihydroxykaur-16-en-15-one (3) and ent-18-acetoxy-7alpha,14beta-dihydroxykaur-16-en-15-one (4), were isolated from the leaves of Croton tonkinensis in a search for inhibitors of NF-kappaB activation and nitric oxide production. These ent-kauranoids inhibited LPS-induced NF-kappaB activation in murine macrophage RAW264.7 cells at IC50 values between 0.07 and 0.42 microM. Consistently, the ent-kauranoids markedly reduced LPS-induced NO production in a comparable concentration-dependent manner.
为了寻找NF-κB激活和一氧化氮产生的抑制剂,从东京巴豆的叶子中分离出四种对映-贝壳杉烷二萜类化合物,其中包括两种已知化合物,对映-7α,14β-二羟基贝壳杉-16-烯-15-酮(1)和对映-18-乙酰氧基-7α-羟基贝壳杉-16-烯-5-酮(2),以及两种新化合物,对映-1β-乙酰氧基-7α,14β-二羟基贝壳杉-16-烯-15-酮(3)和对映-18-乙酰氧基-7α,14β-二羟基贝壳杉-16-烯-15-酮(4)。这些对映-贝壳杉烷类化合物在小鼠巨噬细胞RAW264.7细胞中抑制LPS诱导的NF-κB激活,IC50值在0.07至0.42微摩尔之间。同样,对映-贝壳杉烷类化合物以类似的浓度依赖性方式显著降低LPS诱导的NO产生。