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来自光叶番荔枝果实的新对映-贝壳杉烷类化合物及其对脂多糖刺激的RAW264.7巨噬细胞中一氧化氮产生的抑制作用。

New ent-kauranes from the fruits of Annona glabra and their inhibitory nitric oxide production in LPS-stimulated RAW264.7 macrophages.

作者信息

Nhiem Nguyen Xuan, Hien Nguyen Thi Thu, Tai Bui Huu, Anh Hoang Le Tuan, Hang Dan Thi Thuy, Quang Tran Hong, Kiem Phan Van, Minh Chau Van, Ko Wonmin, Lee Seungjun, Oh Hyuncheol, Kim Seung Hyun, Kim Young Ho

机构信息

Institute of Marine Biochemistry, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam.

Institute of Marine Biochemistry, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam; College of Pharmacy, Chungnam National University, Daejeon 305-764, Republic of Korea.

出版信息

Bioorg Med Chem Lett. 2015 Jan 15;25(2):254-8. doi: 10.1016/j.bmcl.2014.11.059. Epub 2014 Nov 27.

Abstract

Three new ent-kaurane diterpenoids, 7β,16α,17-trihydroxy-ent-kauran-19-oic acid (1), 7β,17-dihydroxy-16α-ent-kauran-19-oic acid 19-O-β-d-glucopyranoside ester (2), 7β,17-dihydroxy-ent-kaur-15-en-19-oic acid 19-O-β-d-glucopyranoside ester (3) along with five known compounds, paniculoside IV (4), 16α,17-dihydroxy-ent-kaurane (5), 16β,17-dihydroxy-ent-kaurane (6), 16β,17-dihydroxy-ent-kauran-19-al (7), and 16β,17-dihydroxy-ent-kauran-19-oic acid (8) were isolated from the fruits of Annona glabra. Their chemical structures were elucidated by physical and chemical methods. All compounds were evaluated for inhibitory activity against nitric oxide (NO) production in LPS-stimulated RAW 264.7 macrophages. As the results, compound 3 showed potent inhibitory LPS-stimulated NO production in RAW 264.7 macrophages with the IC50 value of 0.01±0.01μM; compounds 1 and 7 showed significant inhibitory NO production with the IC50 values of 0.39±0.12μM and 0.32±0.04μM, respectively.

摘要

从光滑番荔枝果实中分离出三种新的对映-贝壳杉烷二萜类化合物,即7β,16α,17-三羟基-对映-贝壳杉烷-19-酸(1)、7β,17-二羟基-16α-对映-贝壳杉烷-19-酸19-O-β-D-吡喃葡萄糖苷酯(2)、7β,17-二羟基-对映-贝壳杉-15-烯-19-酸19-O-β-D-吡喃葡萄糖苷酯(3),以及五种已知化合物,即paniculoside IV(4)、16α,17-二羟基-对映-贝壳杉烷(5)、16β,17-二羟基-对映-贝壳杉烷(6)、16β,17-二羟基-对映-贝壳杉烷-19-醛(7)和16β,17-二羟基-对映-贝壳杉烷-19-酸(8)。通过物理和化学方法阐明了它们的化学结构。对所有化合物进行了抑制脂多糖(LPS)刺激的RAW 264.7巨噬细胞中一氧化氮(NO)产生的活性评价。结果表明,化合物3对LPS刺激的RAW 264.7巨噬细胞中NO的产生具有强效抑制作用,IC50值为0.01±0.01μM;化合物1和7对NO的产生也有显著抑制作用,IC50值分别为0.39±0.12μM和0.32±0.04μM。

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