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1 le density is apparent only in S1 and S2 for antipain.
2 ation of a new analogue of antipain, deimino-antipain.
3 leupeptin (5 mM) and completely prevented by antipain (2.5 mM).
4  possesses interesting anti-inflammatory and antipain activities.
5                            The P1 arginyl of antipain also binds at this site, but the positive charg
6 e activity was most effectively inhibited by antipain and 4-(2-aminoethyl) benzenesulfonyl fluoride,
7                       The peptide aldehydes, antipain and chymostatin, form covalent adducts with the
8  Moreover, ColV-1 processing is inhibited by antipain and N-ethylmaleimide.
9 eptide ulleungdin, the non-ribosomal peptide antipain and the osmoprotectant ectoine.
10 in, pancreatic trypsin inhibitor, leupeptin, antipain, and EDTA could not prevent histatin 5, stather
11  candidate compounds, avoralstat, PCI-27483, antipain, and soybean trypsin inhibitor, inhibited TMPRS
12                                  The CPD-WII antipain arginine model has a standard crystallographic
13               Antiviral and antiinflammatory-antipain assays have targeted various classes of chemica
14 ing, peptidic protease inhibitors, including antipain, chymostatin, leupeptin, elastatinal, and micro
15 g to the identification of a new analogue of antipain, deimino-antipain.
16 ex with the oligopeptide, protease-inhibitor antipain, giving detailed information on the enzyme acti
17 nyl fluoride (3 mm), leupeptin (100 microm), antipain (IC(50) = 2 microm), HgCl(2) (IC(50) = 500 micr
18                              Pefabloc SC and antipain inhibited the proteolytic activity of both fI a
19 ntration-dependent and could be inhibited by antipain, N-ethylmaleimide, EDTA, and EGTA.
20                     Opioid receptors mediate antipain responses in both the peripheral nervous system
21                            The inhibition by antipain suggested the presence of cysteine or serine pr
22            The bacterial producer of deimino-antipain was sequenced and the responsible biosynthetic