Title:Oteseconazole: First Approved Orally Bioavailable and Selective
CYP51 Inhibitor for the Treatment of Patients with Recurrent
Vulvovaginal Candidiasis
Volume: 30
Issue: 37
关键词:
抗真菌药物,作用机制,真菌羊毛甾醇去甲基酶,阴道炎,甾醇生物合成,奥替康唑。
摘要: Oteseconazole was approved by the US FDA in April 2022. It is the first approved
selective and orally bioavailable CYP51 inhibitor for the treatment of patients with
recurrent Vulvovaginal candidiasis. Herein, we describe its dosage, administration, chemical
structure, physical properties, synthesis, mechanism of action, and pharmacokinetics.