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. 2020 May 8;10:7826. doi: 10.1038/s41598-020-64832-5

Table 1.

Percent change in PGE2 by the treatment of the inhibitors targeting Arachidonic acid cascade, ERK MAPK pathway, and p38 and JNK MAPK pathway.

Pathway Target Compound Percent change (%)
Arachidonic acid cascade (FDR = 0.086) COX-1 Sulindac sulphide −89.1
COX-1 Valeryl salicylate −55.4
COX-2 NS-398 −90.2
COX Sodium salicylate −8.7
PLA2 cPLA2inhibitor −78.9
PLA2 OBAA −29.9
lipoxygenase Nordihydroguaiaretic acid (NDGA) −28.7
12, 15-lipoxygenase ETYA −73.4
12-lipoxygenase Baicalein −68.0
MAPK (ERK) pathway (FDR = 0.067) MEK PD 98059 −76.3
MEK U0126 −69.1
MAPK ERK inhibitor II −50.0
MEK MEK inhibitor I −78.2
Raf RAF1 kinase inhibitor I −72.5
Raf ZM 336372 −48.2
Tpl2 Tpl2 kinase inhibitor 26.2
BRAF Vemurafenib −69.1
MAPK (p38 and JNK) pathway (FDR = 0.067) JNK SP600125 −53.9
p38 (MAPK) PD169316 −82.0
p38 (MAPK) SB 203580 −73.0
JNK JNK inhibitor VIII −12.4
p38 SB202190 −68.3
p38 SB239063 −57.6