ライフサイエンスコーパス: diethylamide

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1 eprotonating the parent nitrile with lithium diethylamide.

2 th the prototypic hallucinogen lysergic acid diethylamide.

3 5-HT2A receptors by using [3H]lysergic acid diethylamide.

4 nM), mesulergine (100 nM) and lysergic acid diethylamide (1 microM) significantly reduced or abolish

5 propanoyl and (Ru(II)b'(2)m)(2+) is bis(4,4'-diethylamide-2,2'-bipyridine)(4-methyl,4'-carboxylate,2,

6 ceptor autoradiography with 3H-lysergic acid diethylamide (3H-LSD), 3H-8-hydroxy-2-[di-N-propylamine]

7 ies were determined using [3H]-lysergic acid diethylamide ([3H]-LSD) binding to cell membranes of hum

8 the sample, most commonly LSD (lysergic acid diethylamide), amphetamines, Ecstasy (methylenedioxymeth

9 ffinity binding sites for 125I-lysergic acid diethylamide and [3H]mesulergine.

10 erivatives of the best active compounds, the diethylamide and the dipropylamide, were also prepared.

11 ctive forms of the 1-(ethyl)propylamide, the diethylamide, and the dipropylamide (all of the same con

12 Classic hallucinogens such as lysergic acid diethylamide are thought to elicit their psychotropic ac

13 The 1-ethylpropylamide, diethylamide, dipropylamide, and 4-morpholinylamide show

14 pathway, whereas others (e.g., lysergic acid diethylamide) favored the PLA2-AA pathway.

15 group on the bisoxazole system using lithium diethylamide, followed by alkylation with an allylic bro

16 in vivo study, the C-1' active isomer of the diethylamide from the 1-carboxy series was tested in inf

17 11g (R1 = meta-CF(3), Ar2 = 4'biphenyl, R3 = diethylamide) illustrated the potency of this series wit

18 showing that the hallucinogen lysergic acid diethylamide, its precursor ergotamine (ERG), and relate

19 search on psychedelics such as lysergic acid diethylamide (LSD) and dissociative drugs such as phency

20 asked about: use of ayahuasca, lysergic acid diethylamide (LSD) and magic mushrooms; demographics, cu

21 quantitation of (3)H-labeled d-lysergic acid diethylamide (LSD) binding to recombinant human 5-hydrox

22 e is renewed interest in using lysergic acid diethylamide (LSD) in clinical psychiatric research and

23 Lysergic acid diethylamide (LSD) is a non-selective serotonin-receptor

24 Lysergic acid diethylamide (LSD) is the prototypical psychedelic drug,

25 ed to elucidate the effects of lysergic acid diethylamide (LSD) on the human brain but the underlying

26 xy-4-iodoamphetamine (DOI) and lysergic acid diethylamide (LSD) stimulated a head-twitch behavioral r

27 Using the ergoline lysergic acid diethylamide (LSD), and a series of substituted tryptami

28 r 5-HT2A receptor ligands like lysergic acid diethylamide (LSD), in which the amine nitrogen is embed

29 ing mescaline, psilocybin, and lysergic acid diethylamide (LSD), profoundly affect perception, cognit

30 The hallucinogen lysergic acid diethylamide (LSD; 0.1 mg/kg, i.p.) caused a time-depend

31 the conformational selectivity of LSD's key diethylamide moiety.

32 ther drug use (eg, cocaine and lysergic acid diethylamide; odds ratio [OR], 1.73; 95% CI, 1.66-1.80)

33 Using the diethylamide of 3,5-dinitrobenzoic acid as a model compo

34 Replacing the p-diethylamide of the known potent delta opioid receptor s

35 The hallucinogens studied [d-lysergic acid diethylamide, psilocin, bufotenin, and (+/-)-1-(2,5-dime

36 chiral center), and the diastereomer of the diethylamide representing the active form at both C-1' a

37 drugs, such as psilocybin and lysergic acid diethylamide, require the 2AR and resemble some of the c

38 receptor selective agonist BW373U86 with a m-diethylamide resulted in a compound with agonist activit

39 Reactions with the N-based nucleophile diethylamide results in the formation of free diethylnit

40 for the 5-HT2C receptor) and d-lysergic acid diethylamide (selective for the 5-HT2A receptor), revers

41 higher risk of dependence than lysergic acid diethylamide users.

42 Phenylphosphonic acid ethyl ester N,N-diethylamide was subjected to a double modification of i

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