TY - JOUR
T1 - Soluble epoxide hydrolase inhibitory activity from Euphorbia supina rafin
AU - Luyen, Bui Thi Thuy
AU - Thao, Nguyen Phuong
AU - Tai, Bui Huu
AU - Dat, Le Duc
AU - Eun, Kim Ji
AU - Yang, Seo Young
AU - Kwon, Se Uk
AU - Lee, Young Mi
AU - Kim, Young Ho
N1 - Publisher Copyright:
© 2015, Korean Society of Pharmacognosy. All rights reserved.
PY - 2015
Y1 - 2015
N2 - In our search for natural soluble epoxide hydrolase (sEH) inhibitors from plants, an extract of the dried whole plants of Euphorbia supina Rafin was found to significantly inhibit sEH activity in vitro. Phytochemical investigation of E. supina resulted in isolation of 17 compounds (1 - 17), including triterpenes (1 - 4), phenolic compounds (5 - 8), and flavonoid derivatives (9 - 17). The structures of the isolated compounds were established mainly by extensive analysis of the 1D and 2D NMR, and MS data. All of the isolated compounds were evaluated for their sEH inhibitory activity. Among the isolated phenolic compounds, 8 was identified as a significant inhibitor of sEH, with an IC50 value of 15.4 ± 1.3 μM. Additionally, a kinetic analysis of isolated compounds (2, 5, 8 - 11, 13, and 17) indicated that the inhibitory effects of flavonoid derivatives 10 and 11 were of mixed-type, with inhibitory constants (Ki) ranging from 3.6 ± 0.8 to 21.8 ± 1.0 μM, whereas compounds 2, 5, 8, 9, 13, and 17 were non-competitive inhibitors with inhibition Ki values ranging from 3.3 ± 0.2 to 39.5 ± 0.0 μM.
AB - In our search for natural soluble epoxide hydrolase (sEH) inhibitors from plants, an extract of the dried whole plants of Euphorbia supina Rafin was found to significantly inhibit sEH activity in vitro. Phytochemical investigation of E. supina resulted in isolation of 17 compounds (1 - 17), including triterpenes (1 - 4), phenolic compounds (5 - 8), and flavonoid derivatives (9 - 17). The structures of the isolated compounds were established mainly by extensive analysis of the 1D and 2D NMR, and MS data. All of the isolated compounds were evaluated for their sEH inhibitory activity. Among the isolated phenolic compounds, 8 was identified as a significant inhibitor of sEH, with an IC50 value of 15.4 ± 1.3 μM. Additionally, a kinetic analysis of isolated compounds (2, 5, 8 - 11, 13, and 17) indicated that the inhibitory effects of flavonoid derivatives 10 and 11 were of mixed-type, with inhibitory constants (Ki) ranging from 3.6 ± 0.8 to 21.8 ± 1.0 μM, whereas compounds 2, 5, 8, 9, 13, and 17 were non-competitive inhibitors with inhibition Ki values ranging from 3.3 ± 0.2 to 39.5 ± 0.0 μM.
KW - Euphorbia supina
KW - Euphorbiaceae
KW - Soluble epoxide hydrolase
UR - http://www.scopus.com/inward/record.url?scp=84944602851&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:84944602851
SN - 1226-3907
VL - 21
SP - 176
EP - 184
JO - Natural Product Sciences
JF - Natural Product Sciences
IS - 3
ER -