دورية أكاديمية

Sesquiterpene lactone derivatives of KSL-B targeting Arf1-Big1Sec7 interaction

التفاصيل البيبلوغرافية
العنوان: Sesquiterpene lactone derivatives of KSL-B targeting Arf1-Big1Sec7 interaction
المؤلفون: Sergio Ortiz, François Peurois, Euzébio Guimarães Barbosa, Mohamed Selkti, Pascale Lemoine, Jacqueline Cherfils, Raphaël Grougnet, Sabrina Boutefnouchet
المصدر: European Journal of Medicinal Chemistry Reports, Vol 6, Iss , Pp 100090- (2022)
بيانات النشر: Elsevier, 2022.
سنة النشر: 2022
المجموعة: LCC:Pharmacy and materia medica
LCC:Other systems of medicine
مصطلحات موضوعية: Pharmacy and materia medica, RS1-441, Other systems of medicine, RZ201-999
الوصف: The GDP/GTP conformational change of Arf GTPase proteins by different guanine exchange factor GEFs proteins (Big1Sec7, ARNOSec7, Brag1Sec7, etc.), modulates important eukaryotes cell functions, such as secretion, endocytosis, phagocytosis, cytokinesis and cell adhesion. The overproduction and overactivation of Arf1 (a member of the GTPase family) have been linked to tumour development and cancer cell proliferation. We herein report the identification of the natural sesquiterpene lactone ketopelenolide B (KSL-B, 1) as a moderate Arf1-Big1Sec7 inhibitor, evaluated by in silico (Inverse virtual screening) and in vitro (12.5 ​± ​1.3% of nucleotide exchange inhibition at 50 ​μM) approaches. Structural modifications by semisynthesis of 1 (2a-10) were then carried out and predicted in silico to retain the same binding mode. Biochemical assays in vitro detected an improvement in the nucleotide exchange inhibition by 8a to 32.0 ​± ​0.3% at 50 ​μM against Arf1-Big1Sec7 complex. In addition, 8a showed selectivity against others ArfGEF members (ARNOSec7 and BragSec7). This derivative may consequently be considered as a new hit targeting Arf1-Big1Sec7 complex with therapeutic potential, particularly in the field of parasitic diseases.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2772-4174
العلاقة: http://www.sciencedirect.com/science/article/pii/S2772417422000620Test; https://doaj.org/toc/2772-4174Test
DOI: 10.1016/j.ejmcr.2022.100090
الوصول الحر: https://doaj.org/article/49fd9101b00a4736b8b7e124c4f4cef8Test
رقم الانضمام: edsdoj.49fd9101b00a4736b8b7e124c4f4cef8
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:27724174
DOI:10.1016/j.ejmcr.2022.100090