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1 ress and by agents that deplete glutathione (ethacrynic acid).
2 at the indole of Trp38 is less than 4 A from ethacrynic acid.
3 ualitatively, for a second GSH conjugate, GS-ethacrynic acid.
5 tivity for the conjugation of glutathione to ethacrynic acid, a compound that is not recognized by ei
6 ne was inhibited in the presence of 1 microM ethacrynic acid (an inhibitor of glutathione S-transfera
7 nce was abolished when cells were exposed to ethacrynic acid (an inhibitor of GST-Pi), buthionine sul
9 a caspase inhibitor, both were sensitive to ethacrynic acid and CP-424,174, two pharmacological agen
11 1/B2 exhibited GSH-conjugating activity with ethacrynic acid and GSH peroxidase activity with cumene
13 ta unsaturated carbonyl containing compounds ethacrynic acid and parthenolide activated Nrf2 in norma
14 is provided by dinitrophenol, nitrobenzene, ethacrynic acid, and S-hexylglutathione, analogues of xe
15 isothiocyanatostilbene-2,2'-disulfonic acid, ethacrynic acid, and Zn(2+) revealed a pharmacological p
17 inhibitors of anion transport, glyburide and ethacrynic acid, blocked maturation of both caspase-1 an
20 d on an inverted microscope and treated with ethacrynic acid, colchicine, vinblastine, cytochalasin B
21 The crystal structure of the human GST pi-ethacrynic acid complex (2GSS) shows that the indole of
23 inal truncated (Delta209-222) rGST A1-1 with ethacrynic acid (EA) were measured in the presence of va
25 n with the substrate EA-SG, to yield GSH and ethacrynic acid (EA), nor the conjugation reaction betwe
26 either GSH or the conjugate between GSH and ethacrynic acid (EASG) causes this segment to become a s
27 ts, including cytochalasin D, latrunculin A, ethacrynic acid (ECA), a Rho kinase inhibitor (Y-27632),
29 is provided by the electrophilic substrate (ethacrynic acid), electrophilic substrate analogue (dini
30 nst inactivation provided by S-(hydroxyethyl)ethacrynic acid indicates that MOI reacts in the active
34 :protein interactions and also revealed that ethacrynic acid is a novel ligand and inhibitor of MAP2K
35 inomethyl benzoic acid, AMAB) to connect two ethacrynic acid moieties was prepared and decoded via it
36 enyl, dexamethasone, buthionine sulfoximine, ethacrynic acid, or N-acetylcysteine pretreatments, was
37 binding and dissociation of the glutathione-ethacrynic acid product conjugate (GS-EA) to wild-type,
39 the nucleophilic addition reaction of GSH to ethacrynic acid, the H107S substitution has no effect on
40 he loop diuretics furosemide, bumetanide and ethacrynic acid, which block the KCC1 potassium-chloride
41 HT+ formation was decreased 97% by 15 microM ethacrynic acid with no effect on the spontaneous reacti
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