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1 ilable APIs: piroxicam, naproxen sodium, and benzocaine.
2 ously m/z and drift-time-resolved species of benzocaine.
3 ; however, external QX314 and the neutral LA benzocaine (100 microM) did not.
4                One exception to this rule is benzocaine, a neutral LA that fails to produce appreciab
5 brafish (Danio rerio), the use of MS-222 and benzocaine also appears to induce avoidance behaviours i
6                             We conclude that benzocaine and 4-hydroxybenzoate interact with the open
7                           The combination of benzocaine and intubation provides an experimental platf
8 thod involves application of the anaesthetic benzocaine and intubation to maintain ventilation and ox
9                We found that the anaesthetic benzocaine at 50 mg l(-1) was an effective and safe anae
10       A homology model for how lidocaine and benzocaine bind in the closed and open/inactivated chann
11                   Compared with mu1, resting benzocaine block did not change at F1579K, decreased at
12 X-314 (by 17-fold) and much less for neutral benzocaine (by 2-fold).
13 on adulterants, such as procaine, lidocaine, benzocaine, caffeine, and levamisole.
14       The fact that the N-protonated form of benzocaine can be found in the gas phase is owed to kine
15  limit of approximately 0.9 x 10(-6) g/cm(2) benzocaine could be achieved.
16                        Permanently uncharged benzocaine could be docked in the closed conformation as
17 cytes, whereas the neutral local anesthetic, benzocaine, does not, suggesting that a titratable amine
18        Ethyl 4-hydroxybenzoate at 1 mM, like benzocaine, elicited little use-dependent inhibition of
19 by the use of topical anesthetics, such as a benzocaine-gel preparation (BGP).
20 esence and absence of use-dependent block by benzocaine homologs during repetitive pulses.
21 amined the use-dependent phenomenon of three benzocaine homologs: ethyl 4-diethylaminobenzoate, ethyl
22  by cocaine by up to 27-fold and reduced the benzocaine-induced leftward shift in the h(infinity) cur
23  clear separation of action of lidocaine and benzocaine into 2 components that can be related to chan
24 hannel block by the neutral local anesthetic benzocaine is unaffected by the distribution of pi elect
25 gineered site and the covalent attachment of benzocaine-methanethiosulfonate to a cysteine introduced
26 d avoidance behaviours to etomidate, but not benzocaine or MS-222; and rainbow trout (Oncorhynchus my
27  Our plasmene nanosheets were able to detect benzocaine overdose down to a parts-per-billion (ppb) le
28 ion of some of the test compounds over time (benzocaine, phenacetin, metribuzin, phenytoin, thiaclopr
29 6%), with products including pharmaceuticals benzocaine, procainamide and mesalazine, and 4-aminophen
30 dy at early life-stages (before 28 hpf); for benzocaine the TPs comprised >90% of the initial amount
31                                              Benzocaine, the ethyl ester of para-aminobenzoic acid th
32 ons of NavAb reveal high-affinity binding of benzocaine to F203 that is a surrogate for FS6, conserve
33                                          For benzocaine, valproic acid and phenacetin several transfo
34 tivity to lidocaine, QX-314, etidocaine, and benzocaine was assayed under whole-cell, voltage-clamp c