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1 ceptor agonists (salbutamol, procaterol, and fenoterol).
2 GP-12177A as did the addition of the agonist fenoterol.
3 s like morphine, metformin, sumatriptan, and fenoterol.
4 s like metformin, sumatriptan, trospium, and fenoterol.
5 bation of bovine tracheal smooth muscle with fenoterol (10(-7) M) for 2 h increased H(1) receptor mRN
6  relative to epinephrine (100%) were 42% for fenoterol, 4.9% for albuterol, 2.5% for dobutamine, and
7 uterol (5.83 +/- 0.06 and 4.71 +/- 0.16) and fenoterol (6.33 +/- 0.07 and 5.67 +/- 0.05) were less se
8 1 (ISO-beta(1)-AR stimulation) or 0.1 microM fenoterol, a beta(2)-AR agonist (FEN-beta(2)-AR stimulat
9 onists activate both G(s) and G(i) proteins, fenoterol, a full agonist of beta(2)-adrenoceptor, selec
10 8551, but not by CGP 20712A, indicating that fenoterol acts via beta(2)-adrenoceptors.
11 the receptor, and K(i) values determined for fenoterol analogs model much better the cAMP activity of
12 ter understand the molecular interactions of fenoterol analogs with the beta(2)-adrenergic receptor,
13         It is noteworthy that although (R,R)-fenoterol and (R,R)-methoxyfenoterol preferentially acti
14 0 times more potent than L-isoproterenol and fenoterol and 100 times more potent than albuterol.
15                          Some ligands (e.g., fenoterol and cimaterol) were more readily inhibited by
16 ave synthesized a series of stereoisomers of fenoterol and its derivatives and characterized their re
17             We found that the R,R isomers of fenoterol and methoxyfenoterol exhibited more potent eff
18 ible for the species-specific differences in fenoterol and trospium uptake.
19 dobutamine, 0.148 with albuterol, 0.194 with fenoterol, and 0.212 with epinephrine.
20 ency, with ephedrine, dobutamine, albuterol, fenoterol, and epinephrine giving 0, 7, 17, 48, and 55%
21 cluding the single enantiomers of verapamil, fenoterol, and isoproterenol.
22 haled short-acting beta2-agonists albuterol, fenoterol, and terbutaline provide rapid as-needed sympt
23                                 In contrast, fenoterol, another beta2-AR agonist, induced a full posi
24                 The Y361A mutant transported fenoterol but not pirbuterol or other beta(2)-adrenergic
25 d a reversal of the affinity and capacity of fenoterol but not trospium uptake.
26 ther beta2-agonists (salbutamol, formoterol, fenoterol, clenbuterol, or adrenaline).
27 ino group, as essential for the affinity for fenoterol conferred by Cys36.
28 ificantly to the left after 18-h exposure to fenoterol, consistent with the increase in receptor numb
29                                              Fenoterol contains two chiral centers and may exist as f
30 trast to zinterol, stimulation of I(Ca,L) by fenoterol (fen-beta(2)-AR), a beta(2)-AR agonist that ac
31 as coupling efficiency, i.e. epinephrine >/= fenoterol > albuterol > dobutamine > ephedrine.
32 lase, namely epinephrine > or = formoterol = fenoterol > terbutaline = zinterol = albuterol > salmete
33                                              Fenoterol increased both the stability and the transcrip
34                                        Thus, fenoterol increases the expression of airway smooth musc
35                          L-Isoproterenol and fenoterol induced > 90% relaxation (percentage of maxima
36                         Alprenolol inhibited fenoterol-induced beta3-adrenoceptor responses while act
37                                          The fenoterol-induced increase in H(1) receptor mRNA was con
38 tion of H(1) receptor mRNA and augmented the fenoterol-induced increase in H(1) receptor mRNA.
39 treatment with dexamethasone did not prevent fenoterol-induced up-regulation of H(1) receptor mRNA.
40 mation, being purely entropy-driven for each fenoterol isomer, rather than a mixture of entropy and e
41 n a mixture of entropy and enthalpy when the fenoterol isomers binding was determined using [(3)H]CGP
42 effects of the beta(2)-adrenoceptor agonist, fenoterol, on the expression of H(1) receptors at the mR
43 week) administration of the beta2AR agonists fenoterol or zinterol, starting at 2 weeks after MI, red
44      The extent of internalization caused by fenoterol over a 1000-fold range of occupancy was propor
45 hrine and the beta(2) adrenoreceptor agonist fenoterol potently inhibited LPS-induced TNF-alpha and I
46  The two strongest agonists, epinephrine and fenoterol, provoked 11-13-fold increases in the level of
47 ive activation of beta2-AR/G(s) signaling by fenoterol restores the blunted beta2-AR contractile resp
48 s and natural products, such as terbutaline, fenoterol, resveratrol, and catechin.
49 o probe the binding affinity for a series of fenoterol stereoisomers and derivatives.
50  differential G protein selectivities of the fenoterol stereoisomers were further confirmed by photoa
51 occupancy and with various concentrations of fenoterol that gave occupancies from 0.93 to 0.001.
52 ed with the low concentrations (0.2 and 2 nM fenoterol), these concentrations did cause significant d
53 to Leu32 caused reversal of trospium but not fenoterol uptake kinetics. Comparison of the uptake of s
54      We found that the beta2-adrenergic drug fenoterol was transported with eightfold higher affinity