Pharmacological Importance of Optically Active Tetrahydro-β-carbolines and Synthetic Approaches to Create the C1 Stereocenter

被引:103
作者
Laine, Aino E. [1 ]
Lood, Christopher [1 ]
Koskinen, Ari M. P. [1 ]
机构
[1] Aalto Univ, Sch Chem Tehcnol, Dept Chem, Organ Chem Lab, FI-00076 Aalto, Finland
关键词
tetrahydro-beta-carboline; TH beta C; pharmacological importance; biological activity; C1-substituted TH beta C; PICTET-SPENGLER REACTION; ENANTIOSPECIFIC TOTAL-SYNTHESIS; INDOLE ALKALOIDS; BIOLOGICAL EVALUATION; ASYMMETRIC-SYNTHESIS; POTENT; DERIVATIVES; EUDISTOMINS; RECEPTOR; DESIGN;
D O I
10.3390/molecules19021544
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
1,2,3,4-Tetrahydro-beta-carbolines (TH beta Cs) are a pharmacologically important group of compounds belonging to the indole alkaloids. C1-Substituted optically active TH beta Cs have been the target of extensive synthetic efforts due to the presence of the scaffold in numerous natural products and synthetic targets. This review briefly summarizes the methods to obtain the C1 stereocenter and concentrates on evaluating the pharmacological importance of optically active C1-substituted TH beta Cs, including their PDE5-inhibitory, antimalarial, antiviral and antitumor activities.
引用
收藏
页码:1544 / 1567
页数:24
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