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The partial faunal reserve of Pama is situated in the province of Kompienga, in the South-East of Burkina Faso, with typical Sudanian savanna vegetation. Adjacent to the Arli National Park and the Pendjari National Park, it is part of the so-called WAP complex, one of the largest wildlife areas in West Africa. Up to now, only little has been known about its flora. The present study aimed at reducing this gap in knowledge, and represents an important tool for conservation and research. The list of species was compiled from the surveys carried out from 2001 to 2004, additional relevé data, and herbarium specimens. We found 450 species, which belong to 244 genera and 73 families. The most species-rich family is Poaceae (83 species), followed by Fabaceae (64), Cyperaceae (24), Rubiaceae (22), Euphor- biaceae (20), Combretaceae (15), Asteraceae (14), Caesalpiniaceae (14), Mimosaceae (12), and Convolvulaceae (11).
The significance of data and Artificial Intelligence (AI) has a profound impact on all industries, presenting both challenges and opportunities. Given its power and relevance, AI has not gone unnoticed in the public affairs sector. The upcoming German federal election in 2025 brings discussions about AI to the forefront, raising questions about the extent to which data will drive the public affairs field and how it will be handled.
Since hyperactivity of the protein kinase DYRK1A is linked to several neurodegenerative disorders, DYRK1A inhibitors have been suggested as potential therapeutics for Down syndrome and Alzheimer’s disease. Most published inhibitors to date suffer from low selectivity against related kinases or from unfavorable physicochemical properties. In order to identify DYRK1A inhibitors with improved properties, a series of new chemicals based on [b]-annulated halogenated indoles were designed, synthesized, and evaluated for biological activity. Analysis of crystal structures revealed a typical type-I binding mode of the new inhibitor 4-chlorocyclohepta[b]indol-10(5H)-one in DYRK1A, exploiting mainly shape complementarity for tight binding. Conversion of the DYRK1A inhibitor 8-chloro-1,2,3,9-tetrahydro-4H-carbazol-4-one into a corresponding Mannich base hydrochloride improved the aqueous solubility but abrogated kinase inhibitory activity.