Cassia is a large tropical genus with about 600 species that have been widely used as folk medicines in China and India. This genus has been known to possess various biological activities, e.g. antimicrobial, anti-inflammatory, antioxidant, anti-malarial, anti-mutagenic activity, and anti-fertility etc. Flavonoids, for its broad spectrum of pharmacological activity and low toxicity, have attracted more interest in the development and utilization of natural medicines. The structure and biological activity research of flavonoids extracted from Cassia genus is the first step in the search for new drugs from those plants. This review summarizes the isolation and characterization of flavonoids from various Cassia species, such as Cassia absus, Cassia alata, Cassia fistula, etc. Flavonoids can be extracted from different parts of the plants, such as seed, leaf, stem and pod. Chemical structure research of these flavonoids in extracts has revealed many different types of compounds, which show the complication of the metabolism of Cassia genus. The antidiabetic activities can be found in many Cassia species. The efficiency of extraction method and action mode have been widely investigated. The extract not only can reduce the blood glucose level, but also improve glycogen content. Research show that the methanolic extract is effective in inducing hypoglycemic effects in both type I and II diabetes. Because flavonoids have complex structures, various function points, and unknown pertinence and selectivity for different health conditions, there are still many research areas waiting to be explored, such as to reveal the metabolic pathways of flavonoids in the Cassia genus, and to illustrate the structure-activity relationship between flavonoids and protein. That above-mentioned research will provide the basis for further medicinal development on this genus.

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The joint toxicities of [BMIM]BF4, [BMIM]PF6, and [HMIM]BF4 on acetylcholinesterase (AChE) were systematically investigated by using a progressive approach from 1D single effect point, 2D concentration-response curve (CRC), to 3D equivalent-surface (ES) level. The equipartition equivalent-surface design (EESD) method was used to design 10 ternary mixtures, and the direct equipartition ray (EquRay) design was used to design 15 binary mixtures. The toxicities of ionic liquids (ILs) and their mixtures were determined using the microplate toxicity analysis (MTA) method. The concentration addition (CA), independent action (IA), and co-toxicity coefficient (CTC) were used as the additive reference model to analyze the toxic interaction of these mixtures. The results showed that the Weibull function fitted well the CRCs of the three ILs and their mixtures with the coefficient of determination (R2) greater than 0.99 and root-mean-square error (RMSE) less than 0.04. According to the CTC integrated with confidence interval (CI) method (CTCICI) developed in this study, the 25 mixtures were almost all additive action at 20% and 80% effect point levels. At 50% effect, at least half of the 25 mixtures were slightly synergistic action, and the remaining mixtures were additive action. Furthermore, the ESs and CRCs predicted by CA and IA were all within the CIs of mixture observed ESs and CRCs, respectively. Therefore, the toxic interactions of these 25 mixtures were actually additive action. The joint toxicity of the three ILs can be effectively evaluated by the ES method. We also studied the relationship between the mixture toxicities and component concentration proportions. This study can provide reference data for IL risk assessment of combined pollution.

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