ライフサイエンスコーパス: hallucinogenic

1 luding increased head-twitch response to the hallucinogenic 5-HT(2A) agonist DOI [1-(2,5-dimethoxy-4-

2 he psychosis-like effects induced in mice by hallucinogenic 5-HT(2A) agonists.

3 Administration of the hallucinogenic 5-HT(2A/2C) agonist 1-[2, 5-dimethoxy-4-i

4 FC and attenuates the in vivo actions of the hallucinogenic 5-HT(2A/2C) receptor agonist (-)2,5-dimet

5 investigated using central injections of the hallucinogenic 5-HT2 agonist DOI and the novel 5-HT2A an

6 Administration of a hallucinogenic 5-HT2A /2C receptor agonist, but not a 5-

7 bility that regulation of BDNF expression by hallucinogenic 5-HT2A receptor agonists leads to adaptat

8 ic serotonin(2A) receptors, the key site for hallucinogenic actions.

9 Although it is generally considered that hallucinogenic activity results from 5-HT(2A) receptor a

10 tionally constrained analogues of the potent hallucinogenic agent, N,N-diethyllysergamide, LSD-25.

11 n 5-HT(2A) receptor, the presumed target for hallucinogenic agents, and a receptor affinity profile i

12 s agonist, serotonin, to a synthetic 5-HT2AR hallucinogenic agonist, 2,5-dimethoxy-4-iodoamphetamine

13 Ibogaine, a hallucinogenic alkaloid proposed as a treatment for opia

14 Ibogaine, a hallucinogenic alkaloid with purported anti-addiction pr

15 xygen substituents that are found in typical hallucinogenic amphetamines such as 4b (DOB).

16 cal survey revealed that psychostimulant and hallucinogenic amphetamines, numerous ergoline derivativ

17 different mechanisms may underlie ibogaine's hallucinogenic and anti-addictive effects.

18 HT2A receptors, a proposed site of action of hallucinogenic and atypical antipsychotic drugs.

19 Hallucinogenic and nonhallucinogenic 2AR agonists both r

20 The molecular basis of ligand selectivity of hallucinogenic and nonhallucinogenic compounds of varyin

21 The hallucinogenic chemicals (+/-)-2,5-dimethoxy-4-iodoamphe

22 Ketamine, a mild hallucinogenic class C drug, is the fastest growing 'par

23 Salvinorin A is a naturally occurring hallucinogenic diterpenoid from the plant Salvia divinor

24 of group II mGlu receptor agonists to reduce hallucinogenic drug action in this region is believed to

25 rid" molecules of the two major prototypical hallucinogenic drug classes, the phenethylamines and the

26 oids represent one of the most commonly used hallucinogenic drug classes.

27 r-1, and egr-2 expression in response to the hallucinogenic drug DOI.

28 asing recreational use of this stimulant and hallucinogenic drug has raised concerns about its potent

29 tate, the aura of temporal lobe epilepsy and hallucinogenic drug states.

30 Because hallucinogenic drugs primarily have serotonin(2A) recept

31 The effects of hallucinogenic drugs resemble some of the core symptoms

32 ental evidence links both visual flicker and hallucinogenic drugs to upward and downward modulations

33 s unique cellular responses when targeted by hallucinogenic drugs, and activation of mGluR2 abolishes

34 the free press, an El Greco fallacy fallacy, hallucinogenic drugs, blue bananas, subatomic particles,

35 Like hallucinogenic drugs, full-field flickering visual stimu

36 The effects of hallucinogenic drugs, such as psilocybin and lysergic ac

37 g serotonergic system may mediate ibogaine's hallucinogenic effect; and (4) 18-MC probably has no aff

38 If hallucinogenic effects are correlated with arachidonic a

39 sion in the cerebral cortex in mediating the hallucinogenic effects of 5-HT2A agonists such as DOI is

40 In addition to marked hallucinogenic effects, LSD exerts methylenedioxymethamp

41 Ibogaine, a hallucinogenic indole alkaloid, has been proposed as a t

42 igin - were analysed for the presence of non-hallucinogenic indole compounds.

43 enous neurotransmitter and is not considered hallucinogenic, metabolites of serotonin also have high

44 norin A is the major active component of the hallucinogenic mint plant Salvia divinorum Epling and Ja

45 sure to psilocybin, the active ingredient of hallucinogenic mushrooms.

46 conformationally restricted analogues of the hallucinogenic phenethylamine 1 (2,5-dimethoxy-4-bromoph

47 This also implies, therefore, that the hallucinogenic phenethylamines cannot be directly superi

48 the aromatic methoxy groups in prototypical hallucinogenic phenylalkylamines 1 and 2.

49 he neoclerodane diterpene Salvinorin A, is a hallucinogenic plant in the mint family that has been us

50 etamine [MDMA]), is an amphetamine with some hallucinogenic properties at high doses.

51 Salvinorin A, the active component of the hallucinogenic sage Salvia divinorum, is an apparently s

52 The results indicate that fluorination of hallucinogenic tryptamines generally has little effect o

53 A series of fluorinated analogues of the hallucinogenic tryptamines N,N-diethyltryptamine (DET),