Indolo[2,3-a]quinolizidines and Derivatives: Bioactivity and Asymmetric Synthesis

被引:14
作者
Perez, Maria [1 ,2 ]
Espadinha, Margarida [3 ]
Santos, Maria M. M. [3 ]
机构
[1] Univ Barcelona, Fac Pharm, Organ Chem Lab, E-08028 Barcelona, Spain
[2] Univ Barcelona, Inst Biomed IBUB, E-08028 Barcelona, Spain
[3] Univ Lisbon, Inst Invest Medicamento iMed ULisboa, Fac Farm, P-1649003 Lisbon, Portugal
关键词
Indoloquinolizidines; corynantheine alkaloids; indole alkaloids; natural products; bioactivity; ENANTIOSELECTIVE TOTAL-SYNTHESIS; GEISSOSCHIZINE METHYL-ETHER; ENANTIOSPECIFIC TOTAL-SYNTHESIS; INDOLE ALKALOID MITRAGYNINE; CHIRAL BUILDING-BLOCK; THAI MEDICINAL HERB; GUINEA-PIG ILEUM; UNCARIA-RHYNCHOPHYLLA; FORMAL SYNTHESIS; INDOLOQUINOLIZIDINE-PEPTIDE;
D O I
10.2174/1381612821666151002112934
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Corynantheine alkaloids with a tetracyclic indole[2,3-a]-quinolizidine motif are an important issue in academia and in the life science industries due to their broad bioactivity profile. In particular, the main biological effects described for indoloquinolizidines include analgesic, anti-inflammatory, antihypertensive, and antiarrhythmic activities, as well as inhibition of multiple ion channels, affinity for opioid receptors, and activity against Leishmania. For that reason, in the last decades, numerous efforts have been invested in the development of novel synthetic strategies to obtain the indole[2,3-a]-quinolizidine system. This review focuses on the synthetic methodologies developed to target the most important alkaloids of this family, and highlights the potential use of these alkaloids or analogs to treat several diseases, ranging from cancer to neurodegenerative disorders.
引用
收藏
页码:5518 / 5546
页数:29
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