Steroidal glycosides from Yucca rostrata and Dracaena braunii and their cytotoxic and antimicrobial evaluation

被引:1
作者
Nguyen, Duc Hung [1 ,2 ]
Brugui, Antoine [1 ]
Miyamoto, Tomofumi [3 ]
Dias, Alexandre M. M. [4 ]
Bellaye, Pierre-Simon [5 ]
Collin, Betrand [6 ]
Sautour, Marc [7 ]
Briand, Loic [1 ]
Mitaine-Offer, Anne-Claire [1 ]
机构
[1] Univ Bourgogne, Inst Agro, Ctr Sci Gout & Alimentat, CNRS,INRAE, Dijon, France
[2] Thai Nguyen Univ Educ, Dept Biol, Thai Nguyen 24000, Vietnam
[3] Kyushu Univ, Grad Sch Pharmaceut Sci, Fukuoka, Japan
[4] Ctr Georges Francois Leclerc, Serv Med Nucl, Plateforme Imagerie & Radiotherapie Preclin, Dijon, France
[5] Univ Bourgogne, Inst Agro, Ctr Georges Francois Leclerc,UMR INSERM, Serv Med Nucl,Plateforme Imagerie & Radiotherapie, F-1231 Dijon, France
[6] Univ Bourgogne, Ctr Georges Francois Leclerc, Serv Med Nucl, Plateforme Imagerie & Radiotherapie Preclin, F-6302 Dijon, France
[7] Hop Bocage, Parasitol & Mycol Lab, BP 77908, F-21079 Dijon, France
关键词
Yucca; Dracaena; Steroidal; Glycoside; Antimicrobial; Cytotoxicity; UNDERGROUND PARTS; FUROSTANOL GLYCOSIDES; TRITERPENOID SAPONINS; INHIBITORY-ACTIVITY; RHIZOMES; CONSTITUENTS; GLORIOSA; LEAVES; ELUCIDATION; SPIROSTANOL;
D O I
10.1016/j.bse.2024.104791
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Steroidal glycosides are known to possess a wide range of biological activities such as cytotoxicity and antimicrobial effects. To isolate more of these glycosides to get a better understanding at their structure/activity relationship, and to complete chemotaxonomic information, a cultivated Yucca rostrata was studied, along with a wild and a cultivated Dracaena braunii. Thirteen spiro- and furostan glycosides were isolated from those plants and their structure were elucidated using 1D and 2D NMR. Since they were already reported from other plant species, it allowed us to get an idea on which type of structure might be specific to which taxon. The compounds from D. braunii were tested for their antimicrobial activity against Candida albicans, C. glabrata and Staphylococcus aureus. Only compound 12 (CAS 39491-39-9) showed a weak activity on S. aureus with a MIC of 50 mu g/mL. The compounds from Y. rostrata were tested for their cytotoxicity against a CT26 (murine colorectal carcinoma) cell line. The spirostan glycosides 4 (CAS 119459-80-2) and 5 (CAS 164592-97-6) showed an interesting activity with an IC50 of 2.38 mu M and 2.26 mu M, respectively. Comparing the structures of the active versus the inactive ones, we were able to formulate some hypotheses regarding the structure/activity relationships, in accordance with the current literature.
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页数:7
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