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1 nt glucagon-like peptide-1 receptor (GLP-1R) noncompetitive antagonist.
2 s a nicotinic acetylcholine receptor (nAChR) noncompetitive antagonist.
3 nnel based on its prevention by proadifen, a noncompetitive antagonist.
4 to pH sensor of ASIC1a acting as orthosteric noncompetitive antagonist.
5 inistration of phencyclidine (PCP), an NMDAR noncompetitive antagonist.
6 rtial agonists), competitive antagonists, or noncompetitive antagonists.
7 ceptor (nAChR), in which barbiturates act as noncompetitive antagonists.
8 effects were observed for the binding of the noncompetitive antagonist [(3)H]ethidium when examined i
9 Based upon the inhibition of binding of the noncompetitive antagonist [(3)H]phencyclidine, azietomid
10 centrations, it inhibited the binding of the noncompetitive antagonists [(3)H]tetracaine and [(3)H]ph
11 more potent inhibitor of the binding of the noncompetitive antagonist [3H]phencyclidine (IC50 = 9 mi
12 s (IC50 = 600 microM) and the binding of the noncompetitive antagonist [3H]tetracaine to nAChR-rich m
13 ce, and a specific component, inhibitable by noncompetitive antagonists and localized to the M2 hydro
14 nct protein preparations, in the presence of noncompetitive antagonists, and over a broad range of io
16 sition 6, respectively, were the most potent noncompetitive antagonists at the NMDA receptor with IC5
17 ent nicotinic acetylcholine receptor (nAChR) noncompetitive antagonist, binds with higher affinity in
18 o- 5H-2,3-benzodiazepine (GYKI 53655) act as noncompetitive antagonists; both drugs act through allos
19 the lipid bilayer can be attenuated by other noncompetitive antagonists, but at concentrations substa
26 igh-affinity binding site for aromatic amine noncompetitive antagonists in the Torpedo nicotinic acet
28 he rate of blocking of NMDA responses by the noncompetitive antagonist MK-801 at the same synapses.
29 receptors was prevented by inclusion of the noncompetitive antagonists MK-801 (2 microM) and GYKI 53
31 ([(125)I]TID) has been shown to be a potent noncompetitive antagonist (NCA) of the nicotinic acetylc
32 fipronil, and the botanical picrotoxinin are noncompetitive antagonists (NCAs) for the GABA receptor.
33 and [(3)H]tetracaine, an aromatic amine, are noncompetitive antagonists (NCAs) of the Torpedo species
35 yl)-vinyl]-6-fluoro- 3H-quinazolin-4-one), a noncompetitive antagonist of AMPA-selective glutamate re
39 VSMC proliferation is inhibited by Mk-801, a noncompetitive antagonist of the N-methyl-D-aspartate (N
43 n for the fluorophor crystal violet (CrV), a noncompetitive antagonist of the nicotinic acetylcholine
46 tion of L-arginine, the effects of MK-801, a noncompetitive antagonist of the NMDA receptor and of LY
51 cluding long chain aliphatic alcohols act as noncompetitive antagonists of the nicotinic acetylcholin
52 dine and its potent congener dizocilpine are noncompetitive antagonists of the NMDA receptor complex,
54 this pattern of fluorescence change, but the noncompetitive antagonist picrotoxin failed to elicit op
55 receptor, as assessed by the effects of the noncompetitive antagonist proadifen on conotoxin binding
56 ors, CT32521 and CT32228, two small-molecule noncompetitive antagonists representing two different cl
59 Several compounds were found to bind to the noncompetitive antagonist site of the AChR as demonstrat
60 similar structure bind to the high-affinity noncompetitive antagonist site of the AChR associated wi
61 abeling experiments using well-characterized noncompetitive antagonists such as the phencyclidine ana
62 was reduced in the presence of proadifen, a noncompetitive antagonist that desensitizes the receptor
63 -(phenylethynyl)-pyridine (MPEP) is a potent noncompetitive antagonist that is selective for mGluR5.
64 ate that the steroid promegestone is an AChR noncompetitive antagonist that may alter AChR function b
66 Whereas cocaine itself is a general nAChR noncompetitive antagonist, we report here the characteri
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