PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23250922-0	2013	beta-Sitosterol oxidation products attenuate vasorelaxation by increasing reactive oxygen species and cyclooxygenase-2.	gamma-sitosterol	0-15	prostaglandin-endoperoxide synthase 2	Homo sapiens	102-118	
23640957-5	2014	Also, beta-sitosterol attenuated the phosphorylation of AKT, mammalian target of rapamycin and S6K, and the expression of cyclooxygenase-2 and VEGF in U266 cells.	gamma-sitosterol	6-21	prostaglandin-endoperoxide synthase 2	Homo sapiens	122-138	
34754315-10	2021	Molecular docking results showed that quercetin, luteolin, kaempferol, tanshinone IIa, wogonin, naringenin, nobiletin, dihydrotanshinlactone, beta-sitosterol, and salviolone have good affinity with core target proteins IL6, PTGS2, MAPK1, MAPK3, and CGRP1.	gamma-sitosterol	142-157	prostaglandin-endoperoxide synthase 2	Homo sapiens	224-229	
35510223-13	2022	The molecular docking results showed that there was a certain affinity between the main compounds (kaempferol, quercetin, beta-sitosterol, naringenin) and core target genes (PTGS2, CASP3, MAPK1, MAPK3, TP53).	gamma-sitosterol	122-137	prostaglandin-endoperoxide synthase 2	Homo sapiens	174-179	
32854331-9	2020	In our network, GO and KEGG results yielded two compounds (beta-sitosterol (BS) and pelargonidin (PG)), targets (PTGS1 (COX-1) and PTGS2 (COX-2)), and pathways (nitric oxide, TNF) were involved in the inhibitory effects of FT on influenza-associated inflammation.	gamma-sitosterol	59-74	prostaglandin-endoperoxide synthase 2	Homo sapiens	131-136	
32854331-9	2020	In our network, GO and KEGG results yielded two compounds (beta-sitosterol (BS) and pelargonidin (PG)), targets (PTGS1 (COX-1) and PTGS2 (COX-2)), and pathways (nitric oxide, TNF) were involved in the inhibitory effects of FT on influenza-associated inflammation.	gamma-sitosterol	76-78	prostaglandin-endoperoxide synthase 2	Homo sapiens	131-136	
34149863-13	2021	SCDP key active ingredients are mainly quercetin, wogonin, baicalein, acacetin, oroxylin A, and beta-sitosterol, which function mainly by regulating targets, such as PTGS2, CASP3, TP53, IL-6, TNF, and AKT1, and are associated with multiple signaling pathways as pathways in cancer, PI3K-Akt signaling pathway, apoptosis, IL-17 signaling pathways.	gamma-sitosterol	96-111	prostaglandin-endoperoxide synthase 2	Homo sapiens	166-171