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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/14967


    Title: Synthesis and structure–activity relationship of salvinal derivatives as potent microtubule inhibitors
    Authors: Chang, CI;Hsieh, CC;Wein, YS;Kuo, CC;Chang, CY;Lung, J;Cherng, JY;Chu, PC;Chang, JY;Kuo, YH
    Contributors: Institute of Biotechnology and Pharmaceutical Research;National Institute of Cancer Research
    Abstract: Salvinal is a natural lignan isolated from the roots of Salvia mitorrhiza Bunge (Danshen). Previous studies have demonstrated its anti-proliferative activity in both drug-sensitive and -resistant cancer cell lines, with IC50 values ranging from 4–17 µM. In this study, a series of salvinal derivatives was synthesized and evaluated for the structure–activity relationship. Among the twenty-four salvinal derivatives, six compounds showed better anticancer activity than salvinal. Compound 25 displayed excellent anticancer activity, with IC50 values of 0.13–0.14 µM against KB, KB-Vin10 (overexpress MDR/Pgp), and KB-7D (overexpress MRP) human carcinoma cell lines. Based on our in vitro microtubule depolymerization assay, compound 25 showed depolymerization activity in a dose-dependent manner. Our findings indicate that compound 25 is a promising anticancer agent with depolymerization activity that has potential for the management of malignance.
    Date: 2023-03-28
    Relation: International Journal of Molecular Sciences. 2023 Mar 28;24(7):Article number 6386.
    Link to: http://dx.doi.org/10.3390/ijms24076386
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1422-0067&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000969703600001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85152321890
    Appears in Collections:[張俊彥] 期刊論文
    [郭靜娟] 期刊論文
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