Seo, Kyoung Hee Jang, Bo Ko Yeon, Seul Ki Kim, Hyeon Ji Lee, Ye Rim Seo, Ran Lee, Wok-Joo Kim, Yoowon Lee, Elijah Hwejin Lee, Dong-Gi Lee, Han-Seung Park, Jong-Hyun Shim, Won-Sik Lee, Jong-Seung Choi, Ji Won Park, Ki Duk 2026-01-15T10:00:52Z 2026-01-15T10:00:52Z 2026-01-12 2026-01 0022-2623 https://pubs.kist.re.kr/handle/201004/154055 Atopic dermatitis (AD) is a chronic inflammatory skin disease driven by immune dysregulation, in which thymic stromal lymphopoietin (TSLP) plays a critical role by triggering type 2 inflammation and exacerbating disease progression. In this study, a screening of our in-house library for inhibition of CCL17 mRNA expression led to identification of hit compound 6a. Based on this scaffold, benzyloxy benzylamide derivatives were systematically designed and synthesized, followed by the evaluation of their anti-inflammatory potential. Among them, compound 14o exhibited the most potent inhibition of CCL17 and IL-1B mRNA expression in HaCaT keratinocytes, along with favorable drug-like properties. 14o interfered with TSLP receptor dimerization and suppressed the TSLP-induced signal transducer and activator of transcription 5 phosphorylation. Furthermore, 14o significantly attenuated TSLP-induced calcium influx and effectively alleviated pruritus and AD-like symptoms in a house dust mite (HDM)-induced AD mouse model. Collectively, these findings highlight 14o as a promising topical therapeutic candidate targeting TSLP signaling for the treatment of AD. English American Chemical Society Synthetic Strategy and Evaluation of the Benzyloxy Benzylamide Derivatives as Thymic Stromal Lymphopoietin Modulators for the Treatment of Atopic Dermatitis Article 10.1021/acs.jmedchem.5c02461 1 Journal of Medicinal Chemistry, v.69, no.2, pp.1154 - 1177 Journal of Medicinal Chemistry 69 2 1154 1177 N scie 001651478100001 Chemistry, Medicinal Pharmacology & Pharmacy Article EPITHELIAL-CELLS TSLP CYTOKINE EXPRESSION INDUCE