AI Article Synopsis

  • - Propolis from Cameroon was studied, leading to the discovery of a new isoflavonol and other compounds, some of which had not been previously identified from propolis.
  • - The compounds were tested for their effects on oxidative stress, with one (2-hydroxy-8-prenylbiochanin A) showing significant inhibition of nitric oxide production and others demonstrating higher reactive oxygen species inhibition than ibuprofen.
  • - Cytotoxicity and antifungal activities were also assessed, revealing moderate cytotoxicity for some extracts and lower antifungal efficacy compared to standard treatments like fluconazole.

Article Abstract

Propolis is rich in diverse bioactive compounds. Propolis samples were collected from three localities of Cameroon and used in the study. Column chromatography separation of propolis MeOH:DCM (50:50) extracts yielded a new isoflavonol, 2-hydroxy-8-prenylbiochanin A (1) alongside 2',3'-dihydroxypropyltetraeicosanoate (2) and triacontyl -coumarate (3) isolated from propolis for first time together with seven compounds: β-amyrine (4), oleanolic acid (5), β-amyrine acetate (6), lupeol (7), betulinic acid (8), lupeol acetate (9) and lupenone (10). These compounds were tested for their inhibitory effect on oxidative burst where intracellular reactive oxygen species (ROS) were produced from zymosan stimulated human whole blood phagocytes and on production of nitric oxide (NO) from lipopolysaccharide (LPS) stimulated J774.2 mouse macrophages. The cytotoxicity of these compounds was evaluated on NIH-3 T3 normal mouse fibroblast cells, antiradical potential on 2,2-diphenyl-1-picrylhydrazylhydrazyl (DPPH·) as well as their anti-yeast potential on four selected candida species. Compound 1 showed higher NO inhibition (IC = 23.3 ± 0.3 µg/mL) than standard compound L-NMMA (IC = 24.2 ± 0.8 µg/mL). Higher ROS inhibition was shown by compounds 6 (IC = 4.3 ± 0.3 µg/mL) and 9 (IC = 1.1 ± 0.1 µg/mL) than Ibuprofen (IC = 11.2 ± 1.9 µg/mL). Furthermore, compound displayed moderate level of cytotoxicity on NIH-3 T3 cells, with IC = 5.8 ± 0.3 µg/mL compared to the cyclohexamide IC = 0.13 ± 0.02 µg/mL. Compound 3 showed lower antifungal activity on and , MIC of 125 μg/mL on each strain compared to 50 μg/mL for fuconazole. The extracts showed low antifungal activities ranging from 250 to 500 μg/mL on and and the values of MIC on were 500 μg/mL and above. DPPH* scavenging activity was exhibited by compounds 1 (IC = 15.653 ± 0.335 μg/mL) and 3 (IC = 89.077 ± 24.875 μg/mL) compared to Vitamin C (IC = 3.343 ± 0.271 μg/mL) while extracts showed moderate antiradical activities with IC values ranging from 309.31 ± 2.465 to 635.52 ± 11.05 µg/mL. These results indicate that compounds 1, 6 and 9 are potent anti-inflammatory drug candidates while 1 and 3 could be potent antioxidant drugs.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254033PMC
http://dx.doi.org/10.1016/j.sjbs.2019.11.035DOI Listing

Publication Analysis

Top Keywords

compounds
7
propolis
5
isoflavonol constituents
4
constituents cameroonian
4
cameroonian propolis
4
propolis evaluation
4
evaluation anti-inflammatory
4
anti-inflammatory antifungal
4
antifungal antioxidant
4
antioxidant potential
4

Similar Publications

New cinnamic acid sugar esters as potential UVB filters: Synthesis, cytotoxicity, and physicochemical properties.

Carbohydr Res

January 2025

Department of Biomolecular Sciences, University of Urbino "Carlo Bo", Campus Scientifico E. Mattei, via Ca' Le Suore 2, 61029, Urbino, PU, Italy. Electronic address:

Cinnamic Acid Sugar Ester Derivatives (CASEDs) are a class of natural compounds that exhibit several interesting biological activities. However, to date, no examples of their use in sunscreen formulations have been reported. Here, we describe the synthesis of a series of novel cinnamic acid esters of glucose (4a-g), ribose (4h) and lactose (4i) starting from the respective acetals 3.

View Article and Find Full Text PDF

Relativistic CASPT2/RASPT2 Program along with DIRAC Software.

J Chem Theory Comput

January 2025

Department of Chemistry, Graduate School of Advanced Science and Engineering, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima City, Hiroshima 739-8526, Japan.

Exploring electronic states in actinide compounds is a critical aspect of nuclear science. However, considering relativistic effects and electron correlation in theoretical calculations poses a complex challenge. To tackle this, we developed the CASPT2/RASPT2 program along with the DIRAC program, enabling calculations of electron correlation methods using multiconfigurational perturbation theory with various relativistic Hamiltonians.

View Article and Find Full Text PDF

T-cell prolymphocytic leukemia (T-PLL) is an aggressive lymphoid malignancy with limited treatment options. To discover new treatment targets for T-PLL, we performed high-throughput drug sensitivity screening on 30 primary patient samples ex-vivo. After screening over 2'800 unique compounds, we found T-PLL to be more resistant to most drug classes, including chemotherapeutics, compared to other blood cancers.

View Article and Find Full Text PDF

A novel ternary boride, NiPtB ( = 0.5), was obtained by argon-arc melting of the elements followed by annealing at 750 °C. It exhibits a new structure type with the space group ( = 2.

View Article and Find Full Text PDF

The global dental implant market is projected to reach $9.5 billion by 2032, growing at a 6.5% compound annual growth rate due to the rising prevalence of dental diseases.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!