PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 25213465-8 2014 Ursolic acid also suppressed TNBS-induced COX-2 and iNOS expression as well as NF-kappaB activation in colon tissues. ursolic acid 0-12 cytochrome c oxidase II, mitochondrial Mus musculus 42-47 25168399-11 2015 Importantly, silence of LKB1, AMPK, or iNOS/Cox-2 by small interference RNA transfection reversed UA-induced effects in cultured cells. ursolic acid 98-100 cytochrome c oxidase II, mitochondrial Mus musculus 44-49 26100520-4 2015 The combination of ursolic acid + resveratrol inhibited TPA-induced signaling pathways, including EGFR, STAT3, Src, Akt, Cox-2, Fas, NF-kappaB, p38 MAPK, c-Jun, and JNK1/2 while increasing levels of tumor suppressors, such as p21 and PDCD4, to a greater extent compared with the groups treated with the individual compounds. ursolic acid 19-31 cytochrome c oxidase II, mitochondrial Mus musculus 121-126 24727148-7 2014 Furthermore, western blot analysis showed that UA significantly decreased CYP2E1 expression levels and production of pro-inflammatory markers including TNF-alpha, IL-1beta and COX-2 in CCl(4)-treated mouse liver. ursolic acid 47-49 cytochrome c oxidase II, mitochondrial Mus musculus 176-181 22427843-7 2012 In addition, UA significantly down-regulated the expression levels of cyclin D1 and COX-2 but up-regulated the levels of caspase-3 as revealed by immunohistochemical analysis of tumor tissue sections. ursolic acid 13-15 cytochrome c oxidase II, mitochondrial Mus musculus 84-89 20133359-7 2010 Furthermore, the results also showed that UA significantly reduced the number of activated microglia cells and astrocytes, decreased the expression of CD11b and glial fibrillary acidic protein, downregulated the expression of iNOS and COX-2, and decreased interleukin (IL)-1beta, IL-6, and tumor necrosis factor-alpha levels in the prefrontal cortex of D-gal-treated mice. ursolic acid 42-44 cytochrome c oxidase II, mitochondrial Mus musculus 235-240 31083310-9 2019 Conclusions: 18beta glycyrrhetinic acid, isoliquiritigenin, and ursolic acid inhibited the gene expressions of ICAM-1, TNF-alpha, COX-2, and iNOS, partly through inhibiting NF-kappaB expression and attenuating NF-kappaB nuclear translocation. ursolic acid 64-76 cytochrome c oxidase II, mitochondrial Mus musculus 130-135 16636478-2 2006 In this study, we found that topical applications of UA to mouse skin twice a week for 2 weeks significantly enhanced mRNA expression of cyclooxygenase (COX)-1, COX-2, and tumor necrosis factor-alpha, whereas its effect on tumor promotion was unclear. ursolic acid 53-55 cytochrome c oxidase II, mitochondrial Mus musculus 161-166 9485026-6 1998 The 3-alpha(axial)-epimer of ursolic acid suppressed de novo formation of COX-2, in contrast to naturally occurring 3-beta(equatorial)-ursolic acid. ursolic acid 29-41 cytochrome c oxidase II, mitochondrial Mus musculus 74-79