scholarly journals A new phenolic derivative with soluble epoxide hydrolase and nuclear factor-kappaB inhibitory activity from the aqueous extract of Acacia catechu

2015 ◽  
Vol 30 (18) ◽  
pp. 2085-2092 ◽  
Author(s):  
Ya Nan Sun ◽  
Wei Li ◽  
Seok Bean Song ◽  
Xi Tao Yan ◽  
Yan Zhao ◽  
...  
2012 ◽  
Vol 2 (4) ◽  
Author(s):  
Kuppusamy Asokkumar ◽  
Lokeswari Prathyusha Tangella ◽  
Muthusamy Umamaheshwari ◽  
Thirumalaisamy Shivashanmugam ◽  
Varadharajan Subhadradevi ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (47) ◽  
pp. 40706-40716 ◽  
Author(s):  
Hao-Yu Tang ◽  
Meng-Meng Bai ◽  
Jun-Mian Tian ◽  
Gennaro Pescitelli ◽  
Trpimir Ivšić ◽  
...  

22 compounds, including two rare cage chlorinated iridoids, bungosides A (1) and B (2), were isolated fromCatalpa bungei. of soluble epoxide hydrolase (sEH), acetylcholinesterase (AChE) and BChE, and NF-κB activity.


2014 ◽  
Vol 29 (12) ◽  
pp. 1139-1144 ◽  
Author(s):  
Hang Li ◽  
Zi-Zhe Cai ◽  
Long-Ping Zhu ◽  
Xin-Jun Xu ◽  
Shao-Rui Chen ◽  
...  

2015 ◽  
Vol 23 (20) ◽  
pp. 6659-6665 ◽  
Author(s):  
Ya Nan Sun ◽  
Jang Hoon Kim ◽  
Wei Li ◽  
A. Reum Jo ◽  
Xi Tao Yan ◽  
...  

2012 ◽  
Vol 341 (3) ◽  
pp. 725-734 ◽  
Author(s):  
Yingmei Liu ◽  
Heather K. Webb ◽  
Hisayo Fukushima ◽  
Janine Micheli ◽  
Svetlana Markova ◽  
...  

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
YN Sun ◽  
AR Jo ◽  
JH Kim ◽  
JS Kang ◽  
YH Kim

Molecules ◽  
2017 ◽  
Vol 22 (9) ◽  
pp. 1432 ◽  
Author(s):  
Jang Kim ◽  
Hyo Kim ◽  
Si Kang ◽  
Young Kim ◽  
Chang Jin

2009 ◽  
Vol 8 (8) ◽  
pp. 2193-2203 ◽  
Author(s):  
Jun-Yan Liu ◽  
See-Hyoung Park ◽  
Christophe Morisseau ◽  
Sung Hee Hwang ◽  
Bruce D. Hammock ◽  
...  

2021 ◽  
Vol 14 (12) ◽  
pp. 1323
Author(s):  
Juan Martín-López ◽  
Sandra Codony ◽  
Clara Bartra ◽  
Christophe Morisseau ◽  
María Isabel Loza ◽  
...  

The pharmacological inhibition of soluble epoxide hydrolase (sEH) has been suggested as a potential therapy for the treatment of pain and inflammatory diseases through the stabilization of endogenous epoxyeicosatrienoic acids. Numerous potent sEH inhibitors (sEHI) have been developed, however many contain highly lipophilic substituents limiting their availability. Recently, a new series of benzohomoadamantane-based ureas endowed with potent inhibitory activity for the human and murine sEH was reported. However, their very low microsomal stability prevented further development. Herein, a new series of benzohomoadamantane-based amides were synthetized, fully characterized, and evaluated as sEHI. Most of these amides were endowed with excellent inhibitory potencies. A selected compound displayed anti-inflammatory effects with higher effectiveness than the reference sEHI, TPPU.


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