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1 eITC being almost 100 times more potent than papaverine.
2 mixtures of morphine-papaverine and acridine-papaverine.
3 guinarine and berberine, and the vasodilator papaverine.
4 to berberine and (S)-tetrahydropapaverine to papaverine.
5 l compounds codeine, morphine, noscapine and papaverine.
6 asodilation mediated by ACh and VEGF but not papaverine.
7 GF), and an endothelium-independent agonist, papaverine.
8 usate: PGE1, trifluoperazine, verapamil, and papaverine.
9                                Intracoronary papaverine (20 mg) was used to induce hyperemia.
10                                              Papaverine (30 or 40 microg/kg/min), isoproterenol (0.06
11                   Intracoronary infusions of papaverine (8 mg) and SP were administered before and 20
12                                              Papaverine (a nonnarcotic alkaloid that has been used fo
13                   Responses to 10 micromol/L papaverine, a direct smooth muscle dilator, were impaire
14                         Here, we report that papaverine, a vasodilator, shows inhibitory action again
15 on in sanguinarine, dihydrosanguinarine, and papaverine accumulation in opium poppy roots in support
16  transcript levels also caused a decrease in papaverine accumulation, confirming the selective roles
17 renol (IPNE), arginine vasopressin (AVP), or papaverine, all of which are known to increase tissue cA
18 osphodiesterase (PDE) inhibitors rolipram or papaverine also increased expression of CREB mRNA in hip
19                               Interestingly, papaverine also inhibited paramyxoviruses parainfluenza
20 responses to adenosine were not inhibited by papaverine, an uptake blocker, or by removal of extracel
21 ieved for two component mixtures of morphine-papaverine and acridine-papaverine.
22 ids (morphine, codeine, thebaine, noscapine, papaverine and narceine) in poppy seeds and bakery produ
23 450 potentially involved in the formation of papaverine and noscapine.
24 ient cell lines and that the PDE10 inhibitor papaverine and PDE10A siRNA restored cAMP/PKA signaling.
25  also converted (RS)-tetrahydropapaverine to papaverine and several protoberberine alkaloids to oxidi
26                                              Papaverine and some derivatives were previously shown to
27 use model of mitochondrial optic neuropathy, papaverine and zolpidem provided significant protection
28                                              Papaverine and zolpidem were recently shown to be protec
29               Tetrahydropapaverine (THP) and papaverine are plant natural products with clinically si
30               This study explores the use of papaverine as an effective inhibitor of both influenza v
31 copy (SERS) with microfluidics for detecting papaverine at low concentrations and show that its SERS
32                                            A papaverine based pharmacophore model for PDE10A inhibiti
33                              We propose that papaverine can be a potential candidate to be used as an
34 avernosal injection of the vasorelaxant drug papaverine cause rapid increases in phosphorylated (acti
35         Heterologous biosynthesis of THP and papaverine could play a role in ensuring a stable supply
36 B, undergoes enzymatic hydrolysis to release papaverine derivative P4H and butyrate, collectively inh
37                      It is also inhibited by papaverine, dipyridamole, and SCH51866 at higher doses.
38 sors for the alkaloids tetrahydropapaverine, papaverine, glaucine, rotundine and noscapine.
39                      Biosynthesis of THP and papaverine has not been achieved to date, in part becaus
40                  The weak acid properties of papaverine hydrochloride were investigated, and Raman ba
41    Exact concentrations of nortriptyline and papaverine in donor solution, acceptor solution, and fre
42 (nortriptyline, haloperidol, loperamide, and papaverine) in physiological solutions, urine, and dried
43 alkaloids including morphine, noscapine, and papaverine, in the specialized cytoplasm of laticifers,
44                                     Although papaverine increased total mesenteric blood flow in norm
45                                              Papaverine-induced pial artery vasodilation was unchange
46            Kinetic studies demonstrated that papaverine inhibited influenza virus infection at a late
47 riptyline into aqueous acceptor (96%) and of papaverine into organic FLM (95%) was achieved based on
48                                              Papaverine is a non-narcotic alkaloid found endemically
49                                              Papaverine is a well-known phosphodiesterase inhibitor a
50                  Penile erection elicited by papaverine is reduced profoundly in mice with targeted d
51                                              Papaverine is typically used as a vasorelaxant due to it
52  the drugs atracurium and cisatracurium, and papaverine is used as an antispasmodic during vascular s
53 eatment with the phosphodiesterase inhibitor papaverine led to a mass shift of 80 Da.
54 odulation of host cell signaling pathways by papaverine may be associated with the nuclear retention
55                      A significant effect of papaverine on the influenza virus morphology was observe
56 ssively (2-3 levels) in resting muscles with papaverine or sodium nitroprusside.
57 vasomotor responses to estradiol alone or to papaverine or SP before versus after estradiol.
58 , rolipram, 3-isobutyl-1-methylxanthine, and papaverine) or mimic cAMP (8-bromo-cAMP); the 2- to 4-fo
59                                              Papaverine, phenylephrine, and doxycycline competitively
60       Finally, we demonstrate a strategy for papaverine semisynthesis using hydrogen peroxide as an o
61 rated the ability to produce semisynthesized papaverine through oxidation of biosynthesized THP.
62                                              Papaverine treatment of influenza-virus-infected cells r
63 P) localization was observed as an effect of papaverine treatment.
64    The desired separation for ketoprofen and papaverine was established based on a single experiment.
65 s 25+/-7%; P<0.05, n=6), whereas dilation to papaverine was unchanged.
66 protonated forms of the isoquinoline ring of papaverine were identified.
67 ential of VSMCs to shear stress, H2O2, or to papaverine were recorded with videomicroscopy.
68               Angioplasty and intra-arterial papaverine were used in patients with vasospasm resistan
69 ytes and experimental data of ketoprofen and papaverine were used to test the proposed methodology.
70 gland tumors and found to be as effective as papaverine with an improved safety profile.
71 ke multifunctional modulators by conjugating papaverine with butyrate, a short-chain fatty acid (SCFA
72             Treatment of Ndufs4 KO mice with papaverine, zolpidem, and rapamycin-suppressed inflammat