Hyrtiosin, a novel pyridinium-conjugated indole derivative from vietnamese marine sponge hyrtios erectus.

IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED
Le Viet Ha Tran, Huu Canh Vo, Vinh Han La, Quoc Tuan Le, Minh Canh Nguyen, Duc Trung Le, Thi Thu Hien Do, Huynh Nguyen Khanh Tran
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引用次数: 0

Abstract

The present phytochemical investigation of methanol extract from Vietnamese marine sponge, Hyrtios erectus, resulted to the isolation and structure elucidation of five compounds consisting of a new pyridinium-conjugated indole derivative (hyrtiosin, 1), together with four known alkaloids identified as gramine (2), indole-3-carboxaldehyde (3), 3-(methoxymethyl)indole (4) and N-methylnicotinic acid or trigonelline (5). Chemical structures of isolated compounds were established using modern spectroscopic methods including NMR (1H,13C, COSY, HSQC, HMBC), HR-ESIMS, UV and IR. Compound 1 is rare occurrence of natural products with an acetyl moiety linked to N-1. The isolated compounds were tested with inhibitory activity of NO production and growth of bacterial strains. Among them, only compound 1 displayed the weak inhibition of nitric oxide production with an IC50 value of 38.2 μM, others unfortunately have no activity in both of assays. All of them are first report both of isolation, structural elucidation and bioactivities from specie H. erectus.

hytiosin:一种新型吡啶共轭吲哚衍生物。
对越南海绵Hyrtios erectus甲醇提取物进行了植物化学研究,分离并鉴定了5个化合物,这些化合物由一种新的吡啶共轭吲哚衍生物(hyrtiosin, 1)和4种已知生物碱组成,分别为:gramine(2)、吲哚-3-甲醛(3)、3-(甲氧基甲基)吲哚(4)和n -甲基烟酸或葫芦巴碱(5)。采用NMR (1H,13C, COSY, HSQC, HMBC), HR-ESIMS, UV和IR等现代光谱方法确定了化合物的化学结构。化合物1是罕见的天然产物,其乙酰基片段与N-1相连。对分离得到的化合物进行了抑菌活性测试。其中,只有化合物1对一氧化氮产生的抑制作用较弱,IC50值为38.2 μM,其他化合物在两种检测中均无活性。从直立人的分离、结构鉴定和生物活性方面均为首次报道。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
47
审稿时长
2.3 months
期刊介绍: The Journal of Asian Natural Products Research (JANPR) publishes chemical and pharmaceutical studies in the English language in the field of natural product research on Asian ethnic medicine. The journal publishes work from scientists in Asian countries, e.g. China, Japan, Korea and India, including contributions from other countries concerning natural products of Asia. The journal is chemistry-orientated. Major fields covered are: isolation and structural elucidation of natural constituents (including those for non-medical uses), synthesis and transformation (including biosynthesis and biotransformation) of natural products, pharmacognosy, and allied topics. Biological evaluation of crude extracts are acceptable only as supporting data for pure isolates with well-characterized structures. All published research articles in this journal have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by at least two expert referees.
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