دورية أكاديمية

Leishmanicidal and Cholinesterase Inhibiting Activities of Phenolic Compounds from Allanblackia monticola and Symphonia globulifera

التفاصيل البيبلوغرافية
العنوان: Leishmanicidal and Cholinesterase Inhibiting Activities of Phenolic Compounds from Allanblackia monticola and Symphonia globulifera
المؤلفون: Bruno Ndjakou Lenta, Catherine Vonthron-Sénécheau, Bernard Weniger, Krishna Prasad Devkota, Joseph Ngoupayo, Marcel Kaiser, Qamar Naz, Muhammad Iqbal Choudhary, Etienne Tsamo, Norbert Sewald
المصدر: Molecules; Volume 12; Issue 8; Pages: 1548-1557
بيانات النشر: Molecular Diversity Preservation International
سنة النشر: 2007
المجموعة: MDPI Open Access Publishing
مصطلحات موضوعية: Allanblackia monticola, Symphonia globulifera, Phenolic compounds, Leishmanicidal, Anticholinesterase
جغرافية الموضوع: agris
الوصف: In a preliminary antiprotozoal screening of several Clusiaceae species, the methanolic extracts of Allanblackia monticola and Symphonia globulifera showed high in vitro leishmanicidal activity. Further bioguided phytochemical investigation led to the isolation of four benzophenones: guttiferone A (1), garcinol (2), cambogin (3) and guttiferone F (4), along with three xanthones: allanxanthone A (5), xanthone V1 (6) and globulixanthone C (7) as active constituents. Compounds 1 and 6 were isolated from S. globulifera leaves, while compounds 2-5 were obtained from A. monticola fruits. Guttiferone A (1) and F (4) showed particulary strong leishmanicidal activity in vitro, with IC50 values (0.2 μM and 0.16 μM, respectively) comparable to that of the reference compound, miltefosine (0.46 μM). Although the leishmanicidal activity is promising, the cytotoxicity profile of these compounds prevent at this state further in vivo biological evaluation. In addition, all the isolated compounds were tested in vitro for their anticholinesterase properties. The four benzophenones showed potent anticholinesterase properties towards acetylcholinesterase (AChE) and butylcholinesterase (AChE). For AChE, the IC50 value (0.66 μM) of garcinol (2) was almost equal to that of the reference compound galanthamine (0.50 μM). Furthermore, guttiferone A (1) and guttiferone F (4) (IC50 = 2.77 and 3.50 μM, respectively) were more active than galanthamine (IC50 = 8.5) against BChE.
نوع الوثيقة: text
وصف الملف: application/pdf
اللغة: English
العلاقة: Natural Products Chemistry; https://dx.doi.org/10.3390/12081548Test
DOI: 10.3390/12081548
الإتاحة: https://doi.org/10.3390/12081548Test
حقوق: https://creativecommons.org/licenses/by/3.0Test/
رقم الانضمام: edsbas.8BCAA565
قاعدة البيانات: BASE