Department of Pharmaceutical Technology, Kulliyyah of Pharmacy, International Islamic University Malaysia, Jalan Istana, Bandar Indera Mahkota, Kuantan, Pahang, Malaysia.
Asian Pac J Trop Med. 2012 Feb;5(2):136-41. doi: 10.1016/S1995-7645(12)60012-1.
To study the chemical constituents of stembark of Garcinia malaccensis (G. malaccensis) together with apoptotic, antimicrobial and antioxidant activities.
Purification and structure elucidation were carried out by chromatographic and spectroscopic techniques, respectively. MTT and trypan blue exclusion methods were performed to study the cytotoxic activity. Antibacterial activity was conducted by disc diffusion and microdilution methods, whereas antioxidant activities were done by ferric thiocyanate method and DPPH radical scavenging.
The phytochemical study led to the isolation of α,β-mangostin and cycloart-24-en-3β-ol. α-Mangostin exhibited cytotoxic activity against HSC-3 cells with an IC(50) of 0.33 μM. β- and α-mangostin showed activity against K562 cells with IC(50) of 0.40 μM and 0.48 μM, respectively. α-Mangostin was active against Gram-positive bacteria, Staphylococcus aureus (S. aureus) and Bacillus anthracis (B. anthracis) with inhibition zone and MIC value of (19 mm; 0.025 mg/mL) and (20 mm; 0.013 mg/mL), respectively. In antioxidant assay, α-mangostin exhibited activity as an inhibitor of lipid peroxidation.
G. malaccensis presence α- and β-mangostin and cycloart-24-en-3β-ol. β-Mangostin was found very active against HSC-3 cells and K562. The results suggest that mangostins derivatives have the potential to inhibit the growth of cancer cells by inducing apoptosis. In addition, α-and β-mangostin was found inhibit the growth of Gram-positive pathogenic bacteria and also showed the activity as an inhibitor of lipid peroxidation.
研究 Garcinia malaccensis(G. malaccensis)茎皮的化学成分及其细胞凋亡、抗菌和抗氧化活性。
采用色谱和光谱技术分别进行分离和结构鉴定。采用 MTT 和台盼蓝排除法研究细胞毒性。采用纸片扩散法和微量稀释法进行抗菌活性检测,采用铁氰化钾法和 DPPH 自由基清除法进行抗氧化活性检测。
植物化学研究导致分离出α,β-倒捻子素和环阿尔廷-24-烯-3β-醇。α-倒捻子素有抗 HSC-3 细胞活性,IC(50)为 0.33 μM。β-和α-倒捻子素对 K562 细胞的活性分别为 IC(50)为 0.40 μM 和 0.48 μM。α-倒捻子素对革兰氏阳性菌金黄色葡萄球菌(S. aureus)和炭疽芽孢杆菌(B. anthracis)具有活性,抑菌圈和 MIC 值分别为(19mm;0.025mg/mL)和(20mm;0.013mg/mL)。在抗氧化试验中,α-倒捻子素表现出抑制脂质过氧化的活性。
G. malaccensis 含有α-和β-倒捻子素和环阿尔廷-24-烯-3β-醇。β-倒捻子素对 HSC-3 细胞和 K562 非常活跃。结果表明,倒捻子素衍生物具有通过诱导细胞凋亡抑制癌细胞生长的潜力。此外,α-和β-倒捻子素抑制革兰氏阳性致病菌的生长,并且还表现出抑制脂质过氧化的活性。