Phenolic Derivatives of with Selective MAO-B Inhibition and Mitochondrial Protection.

, also known as (M. Bieb.) Podlech subsp. (Ivanisch.) Réer & Podlech, a Bulgarian endemic species, was investigated for its phenolic profile and neuroprotective potential. A targeted extraction approach led to the isolation of 14 phytochemicals. According to our literature review, none of the isolated chemicals have been reported before for . Two of them are previously undescribed molecules-an isomer of odoratin and 6-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-7-methoxy-4-1-benzopyran-4-one-and four of them had not been observed before our study in the genus : 3'-methoxydaidzein, fujikinetin, sayanedine, and 6,4'-dimethoxy-7,2'-dihydroxyisoflavone. Five of the phytochemicals-maackiain, cajanin, onogenin, afrormosin, and sayanedine-exhibited selective inhibition of human monoamine oxidase-B (MAO-B), with maackiain reducing activity by 45%, nearing the effect of selegiline. The investigated phytochemicals also showed significant antioxidant and neuroprotective effects in ex vivo models using isolated rat brain synaptosomes, mitochondria, and microsomes, mitigating oxidative stress by preserving glutathione levels and reducing lipid peroxidation. Molecular docking confirmed favorable binding of active phytochemicals, particularly maackiain, within the MAO-B active site. Structure-activity relationship (SAR) analysis highlighted the role of specific substituents and fused-ring systems in MAO-B inhibition. This study expands our knowledge of the phytochemical diversity of and supports the therapeutic relevance of its phenolic compounds in neurodegenerative disorders such as Parkinson's disease.