Flavonoids from Acacia pennata and their Cyclooxygenase (COX-1 and COX-2) Inhibitory Activities

Planta Medica ◽  
2007 ◽  
Vol 73 (11) ◽  
pp. 1202-1207 ◽  
Author(s):  
Alain Dongmo ◽  
Tomofumi Miyamoto ◽  
Kazuko Yoshikawa ◽  
Shigenobu Arihara ◽  
Marie-Aleth Lacaille-Dubois
Keyword(s):  
Cox 2 ◽  
2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Isabela Francisca Borges Costa ◽  
Sanderson Dias Calixto ◽  
Marlon Heggdorne de Araujo ◽  
Tatiana Ungaretti Paleo Konno ◽  
Luzineide Wanderley Tinoco ◽  
...  

The genusOcotea(Lauraceae) is distributed mainly in tropical and subtropical regions. Some species of this genus asO. puberulaandO. quixoshave been described in the literature, showing antibacterial activity. AndOcotea macrophyllashowed anti-inflammatory activity with inhibition of COX-1, COX-2, and LOX-5. The purpose of this study was the phytochemical investigation of the plant speciesOcotea notatafrom Restinga Jurubatiba National Park, Macaé, RJ, Brazil, and the search for antimycobacterial fractions and compounds. The crude extract was evaluated for antimycobacterial activity and presented95.75±2.53% of growth inhibition at 100 µg/mL. Then, it was subjected to a liquid-liquid partition and subsequently was chemically investigated by HPLC, revealing the major presence of flavonoids. In this process the partition fractions hexane, ethyl acetate, and butanol are shown to be promising in the antimycobacterial assay. In addition, ethyl acetate fraction was chromatographed and afforded two flavonoids identified by MS and NMR as afzelin and isoquercitrin. The isolated flavonoids afzelin and isoquercitrin were evaluated for their antimycobacterial activity and for their ability to inhibit NO production by macrophages stimulated by LPS; both flavonoids isoquercitrin (Acet22) and afzelin (Acet32) were able to inhibit the production of NO by macrophages. The calculated IC50of Acet22 and Acet32 was 1.03 and 0.85 µg/mL, respectively.


Planta Medica ◽  
2012 ◽  
Vol 78 (18) ◽  
pp. 1942-1948 ◽  
Author(s):  
M. Ramírez-Cisneros ◽  
María Rios ◽  
Ramiro Ríos-Gómez ◽  
A. Aguilar-Guadarrama
Keyword(s):  
Cox 2 ◽  

2015 ◽  
Vol 25 (12) ◽  
pp. 2469-2472 ◽  
Author(s):  
Yong-Ming Yan ◽  
Li-Ji Li ◽  
Xiao-Chu Qin ◽  
Qing Lu ◽  
Zheng-Chao Tu ◽  
...  
Keyword(s):  
Cox 2 ◽  

2019 ◽  
Vol 9 (1) ◽  
pp. 19 ◽  
Author(s):  
Paul Olotu ◽  
Abubakar Ahmed ◽  
Oluyemisi Kunle ◽  
Ijeoma Olotu ◽  
Francis Agwom ◽  
...  

Molecules ◽  
2015 ◽  
Vol 20 (9) ◽  
pp. 15589-15596 ◽  
Author(s):  
Juan Lu ◽  
Qin Sun ◽  
Zheng-Chao Tu ◽  
Qing Lv ◽  
Pi-Xian Shui ◽  
...  

2010 ◽  
Vol 5 (3) ◽  
pp. 1934578X1000500
Author(s):  
Ericsson David Coy Barrera ◽  
Luis Enrique Cuca Suárez

The in vitro anti-inflammatory effect of eight aporphine alkaloids isolated from the leaves of two Lauraceae plants (Pleurothyrium cinereum and Ocotea macrophylla) was evaluated through inhibition of two isozymes of cyclooxygenase (COX-1 and COX-2), 5-lipoxygenase (5-LOX), and platelet aggregation induced by PAF, AA and ADP. All alkaloids exhibited inhibitory activities against COX-2 (IC50 25.9-116 μM range) and PAF- and AA-induced platelet aggregation, while only four and three of them were good COX-1 and 5-LOX inhibitors, respectively. (+)-N-acetyl-nornantenine 6 was the most potent COX-2, 5-LOX, AA and PAF inhibitor.


2015 ◽  
Vol 25 (20) ◽  
pp. 4505-4508 ◽  
Author(s):  
M. Ángeles Ramírez-Cisneros ◽  
María Yolanda Rios ◽  
A. Berenice Aguilar-Guadarrama ◽  
Praveen P.N. Rao ◽  
Rola Aburto-Amar ◽  
...  
Keyword(s):  
Cox 2 ◽  

2020 ◽  
Vol 102 ◽  
pp. 103890
Author(s):  
Nermeen A. Qandeel ◽  
Ashraf K. El-Damasy ◽  
Maha H. Sharawy ◽  
Said M. Bayomi ◽  
Nadia S. El-Gohary

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Vanisree Mulabagal ◽  
Ruby L. Alexander-Lindo ◽  
David L. DeWitt ◽  
Muraleedharan G. Nair

Tea prepared from the aerial parts ofAntigonon leptopusis used as a remedy for cold and pain relief in many countries. In this study,A. leptopustea, prepared from the dried aerial parts, was evaluated for lipid peroxidation (LPO) and cyclooxygenase (COX-1 and COX-2) enzyme inhibitory activities. The tea as a dried extract inhibited LPO, COX-1 and COX-2 enzymes by 78%, 38% and 89%, respectively, at 100 g/mL. Bioassay-guided fractionation of the extract yielded a selective COX-2 enzyme inhibitory phenolic aldehyde, 2,3,4-trihydroxy benzaldehyde. Also, it showed LPO inhibitory activity by 68.3% at 6.25 g/mL. Therefore, we have studied other hydroxy benzaldehydes and their methoxy analogs for LPO, COX-1 and COX-2 enzymes inhibitory activities and found that compound1gave the highest COX-2 enzyme inhibitory activity as indicated by a 50% inhibitory concentration (IC50) at 9.7 g/mL. The analogs showed only marginal LPO activity at 6.25 g/mL. The hydroxy analogs6,7and9showed 55%, 61% and 43% of COX-2 inhibition at 100 g/mL. However, hydroxy benzaldehydes3and12showed selective COX-1 inhibition while compounds4and10gave little or no COX-2 enzyme inhibition at 100 g/mL. At the same concentration, compounds14,21and22inhibited COX-1 by 83, 85 and 70%, respectively. Similarly, compounds18,19and23inhibited COX-2 by 68%, 72% and 70%, at 100 g/mL. This is the first report on the isolation of compound1fromA. leptopustea with selective COX-2 enzyme and LPO inhibitory activities.


2020 ◽  
Vol 17 ◽  
Author(s):  
Deepak Kumar Singh ◽  
Mayank Kulshreshtha ◽  
Yogesh Kumar ◽  
Pooja A Chawla ◽  
Akash Ved ◽  
...  

Background: The pyrazolines give the reactions of aliphatic derivatives, resembling unsaturated compounds in their behavior towards permanganate and nascent hydrogen. This nucleus has been associated with various biological activities including inflammatory. Thiazolinone is a heterocyclic compound that contains both sulfur and nitrogen atom with a carbonyl group in their structure.Thiazolinone and their derivatives have attracted continuing interest because of their various biological activities, such as anti-inflammatory, antimicrobial, anti-proliferative, antiviral, anticonvulsant etc. The aim of the research was to club pyrazoline nucleus with thiazolinone in order to have significantanti-inflammatory activity. The synthesized compounds were chemically characterized for the establishment of their chemical structures and to evaluate as anti-inflammatory agent. Method: In the present work, eight derivatives of substituted pyrazoline (PT1-PT8) were synthesized by a three step reaction.The compounds were subjected to spectral analysis by Infrared, Mass and Nuclear magnetic resonance spectroscopy and elemental analysis data. All the synthesized were evaluated for their in vivo anti-inflammatory activity. The synthesized derivatives were evaluated for their affinity towards target COX-1 and COX-2, using indomethacin as the reference compound molecular docking visualization through AutoDock Vina. Results: Compounds PT-1, PT-3, PT-4 and PT-8 exhibited significant anti-inflammatory activity at 3rd hour being 50.7%, 54.3%, 52.3% and 57% respectively closer to that of the standard drug indomethacin (61.9%).From selected anti-inflammatory targets, the synthesized derivatives exhibited better interaction with COX-1 and COX-2 receptor, where indomethacin showed docking score of -6.5 kJ/mol, compound PT-1 exhibited highest docking score of -9.1 kJ/mol for COX-1 and compound PT-8 having docking score of 9.4 kJ/mol for COX-2. Conclusion: It was concluded that synthesized derivatives have more interaction with COX-2 receptors in comparison to the COX-1 receptors because the docking score with COX-2 receptors were very good. It is concluded that the synthesized derivatives (PT-1 to PT-8) are potent COX-2 inhibitors.


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