Antioxidant and Anti-Protease Activities of Diazepinomicin from the Sponge-Associated Micromonospora Strain RV115

被引:55
作者
Abdelmohsen, Usama Ramadan [1 ,5 ]
Szesny, Matthias [2 ]
Othman, Eman Maher [3 ,6 ]
Schirmeister, Tanja [4 ]
Grond, Stephanie [2 ]
Stopper, Helga [3 ]
Hentschel, Ute [1 ]
机构
[1] Univ Wurzburg, Julius von Sachs Inst Biol Sci, D-97082 Wurzburg, Germany
[2] Univ Tubingen, Inst Organ Chem, D-72076 Tubingen, Germany
[3] Univ Wurzburg, Dept Toxicol, D-97082 Wurzburg, Germany
[4] Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, D-55128 Mainz, Germany
[5] Menia Univ, Fac Pharm, Dept Pharmacognosy, Al Minya 61519, Egypt
[6] Menia Univ, Fac Pharm, Dept Analyt Chem, Al Minya 61519, Egypt
来源
MARINE DRUGS | 2012年 / 10卷 / 10期
关键词
diazepinomicin; anti-protease; antioxidant; actinomycetes; Micromonospora; MARINE NATURAL-PRODUCTS; OXIDATIVE STRESS; CATHEPSIN-L; BIOSYNTHESIS; DERIVATIVES; INHIBITORS;
D O I
10.3390/md10102208
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diazepinomicin is a dibenzodiazepine alkaloid with an unusual structure among the known microbial metabolites discovered so far. Diazepinomicin was isolated from the marine sponge-associated strain Micromonospora sp. RV115 and was identified by spectroscopic analysis and by comparison to literature data. In addition to its interesting preclinical broad-spectrum antitumor potential, we report here new antioxidant and anti-protease activities for this compound. Using the ferric reducing antioxidant power ( FRAP) assay, a strong antioxidant potential of diazepinomicin was demonstrated. Moreover, diazepinomicin showed a significant antioxidant and protective capacity from genomic damage induced by the reactive oxygen species hydrogen peroxide in human kidney (HK-2) and human promyelocytic (HL-60) cell lines. Additionally, diazepinomicin inhibited the proteases rhodesain and cathepsin L at an IC50 of 70-90 mu M. It also showed antiparasitic activity against trypomastigote forms of Trypanosoma brucei with an IC50 of 13.5 mu M. These results showed unprecedented antioxidant and anti-protease activities of diazepinomicin, thus further highlighting its potential as a future drug candidate.
引用
收藏
页码:2208 / 2221
页数:14
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