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1 ticancer and anti-inflammatory properties of ursolic acid.
2 nt with PMA, an effect that was inhibited by ursolic acid.
3 COX-2 promoter, effects that were blocked by ursolic acid.
4 st to naturally occurring 3-beta(equatorial)-ursolic acid.
5  tannic acid, quercetin, oleanolic acid, and ursolic acid.
6 skeletal muscle strength, quality, and mass: ursolic acid (a pentacyclic triterpenoid found in apples
7               We investigated the effects of ursolic acid, a chemopreventive agent, on the expression
8                     Of these compounds, only ursolic acid, a naturally occurring pentacyclic triterpe
9                                              Ursolic acid, a pentacyclic triterpene acid, has been sh
10                                              Ursolic acid also blocked binding of Abeta to microglial
11                                              Ursolic acid also inhibited NF-kappaB-dependent reporter
12                                              Ursolic acid also suppressed the induction of COX-2 mRNA
13 pholide, 18beta-glycyrrhetinic acid, lupeol, ursolic acid and beta-sitosterol showed a strong Th2-inc
14             The naturally occurring compound ursolic acid and the licensed drug ursodeoxycholic acid
15          In addition, these results identify ursolic acid and tomatidine as potential agents and/or l
16                                We found that ursolic acid and tomatidine generate hundreds of small p
17 estingly, a subset of the mRNAs repressed by ursolic acid and tomatidine in aged muscle are positivel
18 stic insight into disease processes, we used ursolic acid and tomatidine to investigate the pathogene
19 scle strength, quality, and mass, similar to ursolic acid and tomatidine.
20                    We therefore propose both ursolic acid as a naturally occurring compound, and urso
21 terpenoids, all derivatives of oleanolic and ursolic acid, as potential anti-inflammatory and chemopr
22 n Illinois reveal theobromine, caffeine, and ursolic acid, biomarkers for species of Ilex (holly) use
23 rrence of abundant triterpenic acids such as ursolic acid but also low concentrated derivatives such
24 nolic acid, propyl gallate, sinapic acid and ursolic acid demonstrated significant inhibition of ABCG
25                                          The ursolic acid effect reached a plateau at ~20 mum, with a
26                         These compounds were ursolic acid, ellipticine, zoxazolamine, and homomoschat
27 riterpenoids such as oleanolic, maslinic and ursolic acids, erythrodiol, and uvaol.
28                          The active compound ursolic acid from HBMe was identified using various spec
29 -inflammatory LNP (NIF-LNP) by incorporating ursolic acid, identified from a natural product library,
30 de C, Zygophylloside G, Zygophylloside K and Ursolic acid), in addition to Oleanolic acid.
31 nhibitory effect of an RORgammat antagonist, ursolic acid, in RORgamma- or RORgammat-dependent cell-b
32                                              Ursolic acid inhibited DNA binding of NF-kappaB consisti
33                                              Ursolic acid inhibited IkappaBalpha degradation, IkappaB
34                                              Ursolic acid inhibited PMA-mediated activation of protei
35     Thus, overall, our results indicate that ursolic acid inhibits IkappaBalpha kinase and p65 phosph
36                   Our data also suggest that ursolic acid is a potential therapeutic agent for AD via
37 lated to ursocholanic acid and dehydro(11,12)ursolic acid lactone.
38  acid and the related compound dehydro(11,12)ursolic acid lactone.
39                             These actions of ursolic acid may mediate its antitumorigenic and chemose
40 s associated with tumorigenesis, but whether ursolic acid mediates its effects through suppression of
41 rocedure was developed for the extraction of ursolic acid, oleanolic acid and oridonin from Rabdosia
42 r CRISPR-KO mechanistic studies uncover that ursolic acid promote endosome acidification by activatin
43                 The 3-alpha(axial)-epimer of ursolic acid suppressed de novo formation of COX-2, in c
44 scribed in the present report, we found that ursolic acid suppressed NF-kappaB activation induced by
45                               Treatment with ursolic acid suppressed PMA-mediated induction of COX-2
46                  Furthermore, the effects of ursolic acid (UA) and oleanolic acid (OA) on the synthes
47                                  Among them, ursolic acid (UA) has attracted attention because of its
48                                              Ursolic acid (UA) has proved to have broad-spectrum anti
49                                              Ursolic acid (UA) is a natural triterpenoid possessing a
50                                              Ursolic acid (UA) is a naturally bioactive product that
51 resent report, we investigated the effect of ursolic acid (UA), a pentacyclic triterpenoid found in r
52 study, Wang et al. demonstrated that feeding ursolic acid (UA), a plant-derived compound, to Caenorha
53                            Here we show that ursolic acid (UA), a small molecule present in herbal me
54         Pentacyclic triterpenoids, including ursolic acid (UA), are bioactive compounds with multiple
55 d a novel combination nanosystem of LMWH and ursolic acid (UA), which is also an angiogenesis inhibit
56                                              Ursolic acid (up to 2.9 g/100 g DW) was the main TA, fol
57 5 mug/g DM) was determined in pear peel, and ursolic acid was predominant.
58 etulinic, corosolic, maslinic, oleanolic and ursolic acids was developed and applied to 38 different