In silico investigation of potential interleukin-8 (IL-8) and Cathelicidin (LL-37) inhibitors for rosacea treatment

被引:1
作者
Fakih, Taufik Muhammad [1 ,2 ]
Hikmawati, Deis [3 ]
Sutedja, Endang [4 ]
Dwiyana, Reiva Farah [4 ]
Atik, Nur [5 ]
Muchtaridi, Muchtaridi [1 ,6 ]
机构
[1] Univ Padjadjaran, Dept Pharmaceut Anal & Med Chem, Fac Pharm, Jalan Raya Bandung Sumedang KM 21, Jatinangor 45363, Indonesia
[2] Univ Islam Bandung, Fac Math & Nat Sci, Dept Pharm, Jl Ranggagading 8, Bandung 40116, Indonesia
[3] Univ Islam Bandung, Fac Med, Dept Dermatol, Jl Tamansari 20, Bandung 40116, Indonesia
[4] Univ Padjadjaran, Dr Hasan Sadikin Hosp, Fac Med, Dept Dermatol & Venereol, Jl Pasteur 38, Bandung 40161, Indonesia
[5] Univ Padjadjaran, Fac Med, Dept Biomed Sci, Jalan Raya Bandung-Sumedang KM 21, Sumedang 45363, Indonesia
[6] Natl Res & Innovat Agcy BRIN, Res Collaborat Ctr Theranost Radiopharmaceut, Jl Raya Bandung Sumedang KM 21, Sumedang 45363, Indonesia
关键词
interleukin-8; rosacea treatment; ZINC molecules; in silico study; structure drug design;
D O I
10.3897/pharmacia.71.e124099
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Emerging clinical observations underscore the correlation between interleukin-8 (IL-8) and rosacea. Increased IL-8 expression has been detected in rosacea samples, particularly in moderate to severe manifestations. This phenomenon has prompted the exploration of IL-8 as a prospective therapeutic target for rosacea treatment. To this end, a selection of compounds sourced from the ZINC database, encompassing six small molecules, was made with the intent of identifying promising lead candidates that exhibit drug-like characteristics against IL-8. Through an integrated in silico approach involving structure-guided drug design, encompassing molecprotein-peptide docking, and scrutiny of toxicity profiles, it was ascertained that the small molecule ZINC000022339916 effectively inhibits IL-8 activity. These findings present a novel lead compound that warrants further validation through in vitro, in vivo, and ongoing clinical investigations to confirm its potential for therapeutic management of rosacea.
引用
收藏
页码:1 / 12
页数:12
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