ライフサイエンスコーパス: papaverine

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1 mixtures of morphine-papaverine and acridine-papaverine.

2 guinarine and berberine, and the vasodilator papaverine.

3 to berberine and (S)-tetrahydropapaverine to papaverine.

4 l compounds codeine, morphine, noscapine and papaverine.

5 asodilation mediated by ACh and VEGF but not papaverine.

6 GF), and an endothelium-independent agonist, papaverine.

7 eITC being almost 100 times more potent than 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 Responses to 10 micromol/L papaverine, a direct smooth muscle dilator, were impaire

13 on in sanguinarine, dihydrosanguinarine, and papaverine accumulation in opium poppy roots in support

14 transcript levels also caused a decrease in papaverine accumulation, confirming the selective roles

15 renol (IPNE), arginine vasopressin (AVP), or papaverine, all of which are known to increase tissue cA

16 osphodiesterase (PDE) inhibitors rolipram or papaverine also increased expression of CREB mRNA in hip

17 responses to adenosine were not inhibited by papaverine, an uptake blocker, or by removal of extracel

18 ieved for two component mixtures of morphine-papaverine and acridine-papaverine.

19 ids (morphine, codeine, thebaine, noscapine, papaverine and narceine) in poppy seeds and bakery produ

20 450 potentially involved in the formation of papaverine and noscapine.

21 ient cell lines and that the PDE10 inhibitor papaverine and PDE10A siRNA restored cAMP/PKA signaling.

22 also converted (RS)-tetrahydropapaverine to papaverine and several protoberberine alkaloids to oxidi

23 use model of mitochondrial optic neuropathy, papaverine and zolpidem provided significant protection

24 Papaverine and zolpidem were recently shown to be protec

25 copy (SERS) with microfluidics for detecting papaverine at low concentrations and show that its SERS

26 A papaverine based pharmacophore model for PDE10A inhibiti

27 avernosal injection of the vasorelaxant drug papaverine cause rapid increases in phosphorylated (acti

28 It is also inhibited by papaverine, dipyridamole, and SCH51866 at higher doses.

29 The weak acid properties of papaverine hydrochloride were investigated, and Raman ba

30 Exact concentrations of nortriptyline and papaverine in donor solution, acceptor solution, and fre

31 Although papaverine increased total mesenteric blood flow in norm

32 Papaverine-induced pial artery vasodilation was unchange

33 riptyline into aqueous acceptor (96%) and of papaverine into organic FLM (95%) was achieved based on

34 Papaverine is a non-narcotic alkaloid found endemically

35 Penile erection elicited by papaverine is reduced profoundly in mice with targeted d

36 eatment with the phosphodiesterase inhibitor papaverine led to a mass shift of 80 Da.

37 ssively (2-3 levels) in resting muscles with papaverine or sodium nitroprusside.

38 vasomotor responses to estradiol alone or to papaverine or SP before versus after estradiol.

39 , rolipram, 3-isobutyl-1-methylxanthine, and papaverine) or mimic cAMP (8-bromo-cAMP); the 2- to 4-fo

40 Papaverine, phenylephrine, and doxycycline competitively

41 The desired separation for ketoprofen and papaverine was established based on a single experiment.

42 s 25+/-7%; P<0.05, n=6), whereas dilation to papaverine was unchanged.

43 protonated forms of the isoquinoline ring of papaverine were identified.

44 ential of VSMCs to shear stress, H2O2, or to papaverine were recorded with videomicroscopy.

45 Angioplasty and intra-arterial papaverine were used in patients with vasospasm resistan

46 ytes and experimental data of ketoprofen and papaverine were used to test the proposed methodology.

47 Treatment of Ndufs4 KO mice with papaverine, zolpidem, and rapamycin-suppressed inflammat

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