Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, PR China.
Surgical Science, Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, United States.
Bioorg Chem. 2022 Apr;121:105692. doi: 10.1016/j.bioorg.2022.105692. Epub 2022 Feb 16.
Twenty-one new iridoids, jatamansidoids A-U (1-12, 21-26, 32, 35 and 36), two new natural ones, jatamansidoids V (37) and W (38), eighteen known ones (13-20, 27-31, 33 and 34), together with three patchoulol-type sesquiterpenoids (39-41), were isolated from the roots and rhizomes of Valeriana jatamansi. Structurally, compounds 1-7 were the first examples of iridoids from V. jatamansi with unique α, β, γ, δ-unsaturated aldehyde fragment between C-11, C-4, C-5, C-9 and C-8; compound 8 was an unprecedented iridoid derivative with a methyl group (Me-10) at C-1, rather than C-8, and its plausible biogenetic pathway was proposed in this paper; compounds 22 and 23 were the first examples of Δ-iridoids simultaneously replaced by oxygen-containing groups at C-3, C-6 and C-7; compound 24 was the first iridoid with both 6,7- and 1,10-epoxy fragments. The structures and absolute configurations of new compounds were elucidated based on extensive spectroscopic techniques and quantum chemical calculation. Furthermore, compounds 13-15 and 39-41 exhibited potent anti-influenza virus activities with H1N1 and H3N2 strains, with IC values of 0.21-1.48 µM.
从缬草中分离得到 21 个新的裂环环烯醚萜类化合物,即 jatamansidoids A-U(1-12、21-26、32、35 和 36)、2 个新的天然产物 jatamansidoids V(37)和 W(38)、18 个已知化合物(13-20、27-31、33 和 34)以及 3 个对映贝壳杉烷型倍半萜类化合物(39-41)。结构上,化合物 1-7 是缬草中具有独特的α,β,γ,δ-不饱和醛片段(C-11、C-4、C-5、C-9 和 C-8 之间)的裂环环烯醚萜类的第一个例子;化合物 8 是一个具有前所未有的 1 位(C-1)而非 8 位甲基(Me-10)的裂环环烯醚萜类衍生物,本文提出了其可能的生物合成途径;化合物 22 和 23 是 C-3、C-6 和 C-7 同时含氧取代的Δ-裂环环烯醚萜类的第一个例子;化合物 24 是第一个同时具有 6,7-和 1,10-环氧片段的裂环环烯醚萜类。根据广泛的光谱技术和量子化学计算,确定了新化合物的结构和绝对构型。此外,化合物 13-15 和 39-41 对 H1N1 和 H3N2 株流感病毒具有很强的抑制活性,IC 值为 0.21-1.48 μM。