Synthesis and Evaluation of the Tetracyclic Ring-System of Isocryptolepine and Regioisomers for Antimalarial, Antiproliferative and Antimicrobial Activities

被引:10
作者
Haheim, Katja S. [1 ]
Lindback, Emil [1 ]
Tan, Kah Ni [2 ]
Albrigtsen, Marte [3 ]
Urdal Helgeland, Ida T. [1 ]
Lauga, Clemence [1 ]
Matringe, Theodora [1 ]
Kennedy, Emily K. [2 ]
Andersen, Jeanette H. [3 ]
Avery, Vicky M. [2 ,4 ,5 ]
Sydnes, Magne O. [1 ]
机构
[1] Univ Stavanger, Dept Chem Biosci & Environm Engn, NO-4036 Stavanger, Norway
[2] Griffith Univ, Griffith Inst Drug Discovery, Discovery Biol, Don Young Rd, Nathan, Qld 4111, Australia
[3] UiT Arctic Univ Norway, Norwegian Coll Fishery Sci, NO-9037 Tromso, Norway
[4] Griffith Univ, CRC Canc Therapeut, Nathan, Qld 4111, Australia
[5] Griffith Univ, Sch Environm & Sci, Nathan, Qld 4111, Australia
来源
MOLECULES | 2021年 / 26卷 / 11期
关键词
indoloquinoline; antiplasmodial activity; antiproliferative activity; antimicrobial activity; biofilm inhibition; MARINE PYRIDOACRIDINE ALKALOIDS; CELL-CYCLE ARREST; IN-VITRO; TOPOISOMERASE-II; CRYPTOLEPIS-SANGUINOLENTA; RESISTANT MALARIA; NATURAL-PRODUCTS; PLANT ALKALOIDS; NEOCRYPTOLEPINE; ANALOGS;
D O I
10.3390/molecules26113268
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
A series of novel quinoline-based tetracyclic ring-systems were synthesized and evaluated in vitro for their antiplasmodial, antiproliferative and antimicrobial activities. The novel hydroiodide salts 10 and 21 showed the most promising antiplasmodial inhibition, with compound 10 displaying higher selectivity than the employed standards. The antiproliferative assay revealed novel pyridophenanthridine 4b to be significantly more active against human prostate cancer (IC50 = 24 nM) than Puromycin (IC50 = 270 nM) and Doxorubicin (IC50 = 830 nM), which are used for clinical treatment. Pyridocarbazoles 9 was also moderately effective against all the employed cancer cell lines and moreover showed excellent biofilm inhibition (9a: MBIC = 100 mu M; 9b: MBIC = 100 mu M).
引用
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页数:22
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