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1 e hydrogenation of alpha-keto esters such as ethyl pyruvate.
3 ts to possible adsorption changes induced by ethyl pyruvate, a common reactant in chiral hydrogenatio
4 te pancreatitis, the same dosing regimen for ethyl pyruvate also ameliorated bacterial translocation
7 Lipid A analog, phospholipid emulsion, and ethyl pyruvate are currently being evaluated for potenti
8 y providing a compelling basis to reposition ethyl pyruvate as a low-cost immunochemotherapy for clin
9 potential were hepatocyte growth factor and ethyl pyruvate, because they seem to protect against or
10 bility to interfere with NF-kappaB function, ethyl pyruvate blocks IDO induction both in vitro and in
12 e that the low-cost, anti-inflammatory agent ethyl pyruvate elicits a potent immune-based antitumor r
15 to evaluate the anti-inflammatory effect of ethyl pyruvate (EP) in a mouse model of lipopolysacchari
19 f this study was to test the hypothesis that ethyl pyruvate (EP), a soluble pyruvate derivative, is e
22 oxidative and ageing aroma compounds such as ethyl pyruvate, furfural or dioxanes in higher concentra
23 so been promising research results involving ethyl pyruvate, glycogen synthase kinase-3 inhibitors an
29 rent that certain pyruvate esters, including ethyl pyruvate, have pharmacological effects, such as su
30 ory formulated a derivative of pyruvic acid, ethyl pyruvate, in a calcium- and potassium-containing b
33 en mice were treated with a 40 mg/kg dose of ethyl pyruvate just before the first dose of cerulein an
35 r volumes of either pyruvate (n = 6 each) or ethyl pyruvate (n = 9) solution made up exactly like lac
36 ansfection or inhibition of HMGB1 release by ethyl pyruvate or other small molecules led predominantl
37 1,2-addition of an alphaC-lithiated O-silyl ethyl pyruvate oxime to benzoquinone, which is followed
38 n mice with a noncytotoxic dosing regimen of ethyl pyruvate shown previously to protect against letha
41 quent studies, we showed that treatment with ethyl pyruvate solution could improve survival in rodent
42 ent with either Ringer's lactate solution or ethyl pyruvate solution on several physiologic and bioch
43 ent of rats with either pyruvate solution or ethyl pyruvate solution significantly ameliorated the de
46 findings that IDO is effectively blocked by ethyl pyruvate treatment deepen emerging links between I
50 ht to determine whether a simple derivative, ethyl pyruvate, would be protective in an animal model o
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