Lehbili Meryem, Alabdul Magid Abdulmagid, Kabouche Ahmed, Voutquenne-Nazabadioko Laurence, Abedini Amin, Morjani Hamid, Gangloff Sophie C, Kabouche Zahia
a Laboratoire d'Obtention des Substances Thérapeutiques (LOST), Département de chimie , Université des frères Mentouri-Constantine , Constantine , Algeria.
b ICMR-UMR CNRS 7312, Groupe Isolement et Structure , Reims , France.
Nat Prod Res. 2018 Nov;32(22):2683-2691. doi: 10.1080/14786419.2017.1378207. Epub 2017 Sep 19.
From the aerial parts of Salvia barrelieri Etl. (Lamiaceae), 12 compounds including a new triterpene, 3β-acetoxy-olean-18-ene-2α-ol, were isolated. Their structures were established by the combination analyses of spectroscopy including 1D-, 2D-NMR and HRESIMS and in comparison with the reported data in the literature. The antibacterial activity of these compounds was evaluated by bioautography on Staphylococcus aureus followed by the determination of MIC values by serial dilution technique against five bacteria. Three compounds were active against Enterococcus faecalis, S. aureus, Staphylococcus epidermidis, Escherichia coli and Pseudomonas aeruginosa (MIC 15.1 to 125 μg/mL). Two compounds showed moderate DPPH radical scavenging activity (IC 79.1 and 21.2 μg/mL). These compounds did not show significant tyrosinase inhibitory activities (IC 1.5 mg/mL). Their cytotoxic activity was evaluated against promyelocytic leukaemia (HL60), human erythromyeloblastoid leukaemia (K562) and fibrosarcoma (HT1080) cell lines and four compounds exhibited a moderate cytotoxic activity (IC 28.75 to 85.0 μM).
从药用鼠尾草(唇形科)的地上部分分离出12种化合物,其中包括一种新的三萜类化合物3β-乙酰氧基-齐墩果-18-烯-2α-醇。通过一维、二维核磁共振和高分辨电喷雾电离质谱等光谱分析方法,并与文献报道的数据进行比较,确定了它们的结构。通过对金黄色葡萄球菌的生物自显影法评估这些化合物的抗菌活性,随后采用系列稀释技术测定其对五种细菌的最低抑菌浓度(MIC)值。三种化合物对粪肠球菌、金黄色葡萄球菌、表皮葡萄球菌、大肠杆菌和铜绿假单胞菌具有活性(MIC为15.1至125μg/mL)。两种化合物表现出中等程度的1,1-二苯基-2-三硝基苯肼(DPPH)自由基清除活性(IC为79.1和21.2μg/mL)。这些化合物未表现出显著的酪氨酸酶抑制活性(IC为1.5mg/mL)。对早幼粒细胞白血病(HL60)、人红白血病(K562)和纤维肉瘤(HT1080)细胞系评估了它们的细胞毒性活性,四种化合物表现出中等程度的细胞毒性活性(IC为28.75至85.0μM)。