A comprehensive annotated checklist of the members of the phytophagous ladybird beetle tribe Epilachnini (Coccinellinae) in China is compiled based on existing published sources and incorporates the latest taxonomic and nomenclatural updates. The checklist documents 176 extant species across 10 genera and provides analyses of regional species richness, distribution, and host plant associations. Regarding regional species richness, Yunnan Province is home to the highest number of species (76), followed by Taiwan (50), Sichuan (48), Guizhou (48), Guangxi (43), Tibet (43), Guangdong (25), Hainan (17), Hubei (17), Hunan (13), Shaanxi (13), Fujian (12), Henan (10), Jiangsu (10), Anhui (7), Shandong (7), Zhejiang (7), Jiangxi (5), Hong Kong (5), Gansu (5), Beijing (4), Hebei (4), Liaoning (3), Shanxi (2), and Chongqing, Jilin, Heilongjiang, Ningxia, and Xinjiang (each with one species). Among the recognized genera, Epilachna Chevrolat, 1837, is currently the most species-rich genera, with 59 species, followed by Afissa Dieke, 1947 (34), Uniparodentata Wang & Cao, 1993 (28), Henosepilachna Li, 1961 (29), Afidentula Kapur, 1958 (10), Diekeana Tomaszewska & Szawaryn, 2015 (9), and Epiverta Dieke, 1947 (4). Additionally, Afidenta Dieke, 1947, Cynegetis Chevrolat, 1837, and Subcoccinella Agassiz & Erichson, 1845 are each represented by a single species. Host plant data are currently available for only 72 species (approximately 41% of the species recorded in China), which are associated with 177 plant species across 34 families. The most frequently recorded host plant families are Solanaceae (43 species), Cucurbitaceae (32), Urticaceae (15), Fabaceae (14), Asteraceae (14), and Poaceae (10), whereas each of the remaining 28 families comprises fewer than 10 host species. For 104 species (59% of the Chinese members of the tribe), host plant associations remain unknown, highlighting a substantial gap in our understanding of their feeding habits.

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The knowledge that natural products (NPs) are potent and selective modulators of important biomacromolecules (e.g., DNA and proteins) has inspired some of the world's most successful pharmaceuticals and agrochemicals. Notwithstanding these successes and despite a growing number of reports on naturally occurring pairs of enantiomers, this area of NP science still remains largely unexplored, consistent with the adage "If you don't seek, you don't find". Statistically, a rapidly growing number of enantiomeric NPs have been reported in the last several years. The current review provides a comprehensive overview of recent records on natural enantiomers, with the aim of advancing awareness and providing a better understanding of the chemical diversity and biogenetic context, as well as the biological properties and therapeutic (drug discovery) potential, of enantiomeric NPs.

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Dihydronaphthofurans (DHNs) are an important class of arene ring-fused furans which are widely found in many natural and non-natural products and drug candidates with relevant biological and pharmacological activities. Furthermore, vinylidene-naphthofurans exhibit photochromic properties when exposed to UV or sun light at room temperature. For these reasons, a vast array of synthetic procedures for the preparation of dihydronaphthofurans including annulation of naphthols with various reagents, cycloaddition reactions ([3 + 2], [4 + 1] and Diels-Alder), intramolecular transannulation, Friedel-Crafts, Wittig, Claisen rearrangement, neophyl rearrangement and other reactions under various conditions have been developed over the past decades. This review aims to describe the different strategies developed so far for the synthesis of dihydronaphthofurans and their applications. After a brief introduction to the types of dihydronaphthofurans and their biological activities, the different synthetic approaches such as chemical, photochemical, and electrochemical, methods are described and organized on the basis of the catalysts and the other reagents employed in the syntheses. The subsequent section focuses on biological and pharmacological applications and photochromic properties of the target compounds.

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Fourteen compounds, including rubiprasin D (1), rubiprasin B (2), rubiprasin C (3), oleanolic acid (4), methyl-5-hydroxy-dinaphtho[1, 2-2'3']furan-7, 12-dione-6-carboxylate (5), rubioncolin C (6), mollugin (7), furomollugin (8), 3-amino-2-methoxycarbonyl-1, 4-naphthoquinone (9), 1-hydroxy-2-methyl-9, 10-anthraquinone (10), 2-hydroxy-6-methyl-9, 10-anthraquinone (11), 1, 4-dihydroxy-2-hydroxymethyl-9, 10-anthraquinone (12), 2-hydroxy-1-methoxy-9, 10-anthraquinone (13), and 1-hydroxy-2-methoxy-6-methyl-9, 10-anthraquinone(14), were isolated from the methanol extract of the roots and rhizomes of Rubia oncotricha using various column chromatographies. Their structures were mainly determined on basis of NMR and MS spectroscopic data analyses. Among them, 1 is a new oleanane triterpene, and compounds 2-5, 9 and 11-13 were obtained from this plant for the first time. Cytotoxic and nematicidal activities of all these compounds were evaluated, and the results showed that only 4, 6, 11 and 12 exhibited cytotoxicities against A549, SGC-7901 and HeLa cancer cell lines. The IC₅₀ of 6 were 19.42, 2.74, 8.07 μmol·L⁻¹, respectively.

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Anthraquinones are a class of aromatic compounds with a 9,10-dioxoanthracene core. So far, 79 naturally occurring anthraquinones have been identified which include emodin, physcion, cascarin, catenarin, and rhein. A large body of literature has demonstrated that the naturally occurring anthraquinones possess a broad spectrum of bioactivities, such as cathartic, anticancer, anti-inflammatory, antimicrobial, diuretic, vasorelaxing, and phytoestrogen activities, suggesting their possible clinical application in many diseases. Despite the advances that have been made in understanding the chemistry and biology of the anthraquinones in recent years, research into their mechanisms of action and therapeutic potential in autoimmune disorders is still at an early stage. In this paper, we briefly introduce the etiology of autoimmune diabetes, an autoimmune disorder that affects as many as 10 million worldwide, and the role of chemotaxis in autoimmune diabetes. We then outline the chemical structure and biological properties of the naturally occurring anthraquinones and their derivatives with an emphasis on recent findings about their immune regulation. We discuss the structure and activity relationship, mode of action, and therapeutic potential of the anthraquinones in autoimmune diabetes, including a new strategy for the use of the anthraquinones in autoimmune diabetes.

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