Anti-cryptosporidial efficacy of tricyclic carbazole aminoalcohols in vitro and in vivo

作者：Mingxiao Liu, Weisi Wang, Qi Zheng, Di Zhang, DongQiang Wang, Chenchen Wang, Jigang Yin, Liping Duan, Guan Zhu · 发表于：International Journal for Parasitology Drugs and Drug Resistance · 年份：2026 · DOI：10.1016/j.ijpddr.2026.100631 · 被引用次数：1 · 研究领域：Parasitic Infections and Diagnostics、Amoebic Infections and Treatments、Parasites and Host Interactions

Cryptosporidiosis is a major cause of diarrheal disease in humans and animals, yet there are no fully effective drugs, particularly for immunocompromised patients. Carbazole aminoalcohols (CAAs) are a relatively unexplored chemical class with reported broad-spectrum antiparasitic activities. Here, we systematically evaluated 36 CAA derivatives for anti-cryptosporidial efficacy. In vitro screening using a 44-h Cryptosporidium parvum infection assay identified eight compounds with low-micromolar EC 50 values (1.53–6.86 μM). The three most potent hits (H1402 at 25 mg/kg/d, and YFM1 and YFM3 at 15 mg/kg/d) were selected for in vivo evaluation in a chronic C. tyzzeri mouse model. Daily oral treatment with these compounds for 7 days reduced fecal oocyst shedding by 65.9–68.1% compared with a 247.5% increase in vehicle controls ( P < 0.01). Paromomycin at 1,000 mg/kg/d, used as a positive control, produced an 84.2% reduction. All three CAAs were generally well tolerated, with only minor weight loss observed in H1402-treated mice. Together, these results demonstrate that CAAs possess reproducible in vitro activity and significant in vivo efficacy against cryptosporidial infection, supporting their potential as lead scaffolds for anti-cryptosporidial drug development. Structural optimization to improve potency, selectivity, and pharmacokinetic properties is warranted to advance CAAs toward preclinical development. • Screened 36 carbazole aminoalcohols for anti- Cryptosporidium activit...