North-West Univ. MAO-A compound 2d

North-West Univ. MAO-A compound 2d: sourced facts only. name: "The 4-chloroisatin substituted series (2a-d) showed exceptional MAO-A inhibition (2d: 0.040 ± 0.002 µM), while the unsubstituted, 5-, 6-, and 7-chloroisatin analogues (1a-e, 3a-c, 4a-b, and 5a-e) demonstrated high potency and selectivity toward MAO-B, the most active being 5d (0.018 ± 0.003 µM; selectivity index = 15 389)." [PMID:42603777]; target: "The 4-chloroisatin substituted series (2a-d) showed exceptional MAO-A inhibition (2d: 0.040 ± 0.002 µM), while the unsubstituted, 5-, 6-, and 7-chloroisatin analogues (1a-e, 3a-c, 4a-b, and 5a-e) demonstrated high potency and selectivity toward MAO-B, the most active being 5d (0.018 ± 0.003 µM; selectivity index = 15 389)." [PMID:42603777]; developer: "Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa." [PMID:42603777]