Title : Anti-inflammatory compounds parthenolide and Bay 11-7082 are direct inhibitors of the inflammasome.

Pub. Date : 2010 Mar 26

PMID : 20093358






4 Functional Relationships(s)
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1 Additional investigations of other NF-kappaB inhibitors revealed that the synthetic I kappaB kinase-beta inhibitor Bay 11-7082 and structurally related vinyl sulfone compounds selectively inhibit NLRP3 inflammasome activity in macrophages independent of their inhibitory effect on NF-kappaB activity. 3-(4-methylphenylsulfonyl)-2-propenenitrile NLR family pyrin domain containing 3 Homo sapiens
2 In vitro assays of the effect of parthenolide and Bay 11-7082 on the ATPase activity of NLRP3 demonstrated that both compounds inhibit the ATPase activity of NLRP3, suggesting that the inhibitory effect of these compounds on inflammasome activity could be mediated in part through their effect on the ATPase activity of NLRP3. 3-(4-methylphenylsulfonyl)-2-propenenitrile NLR family pyrin domain containing 3 Homo sapiens
3 In vitro assays of the effect of parthenolide and Bay 11-7082 on the ATPase activity of NLRP3 demonstrated that both compounds inhibit the ATPase activity of NLRP3, suggesting that the inhibitory effect of these compounds on inflammasome activity could be mediated in part through their effect on the ATPase activity of NLRP3. 3-(4-methylphenylsulfonyl)-2-propenenitrile NLR family pyrin domain containing 3 Homo sapiens
4 In vitro assays of the effect of parthenolide and Bay 11-7082 on the ATPase activity of NLRP3 demonstrated that both compounds inhibit the ATPase activity of NLRP3, suggesting that the inhibitory effect of these compounds on inflammasome activity could be mediated in part through their effect on the ATPase activity of NLRP3. 3-(4-methylphenylsulfonyl)-2-propenenitrile NLR family pyrin domain containing 3 Homo sapiens