ライフサイエンスコーパス: lysergic acid

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1 rompted us to devise an expeditious route to lysergic acid.

2 thwarted the completion of the synthesis of lysergic acid.

3 Lysergic acid amides were prepared from (R,R)-(-)-, (S,S

4 etanserin (100 nM), mesulergine (100 nM) and lysergic acid diethylamide (1 microM) significantly redu

5 Tissue receptor autoradiography with 3H-lysergic acid diethylamide (3H-LSD), 3H-8-hydroxy-2-[di-

6 inding affinities were determined using [3H]-lysergic acid diethylamide ([3H]-LSD) binding to cell me

7 Research on psychedelics such as lysergic acid diethylamide (LSD) and dissociative drugs

8 uestions were asked about: use of ayahuasca, lysergic acid diethylamide (LSD) and magic mushrooms; de

9 ng method for quantitation of (3)H-labeled d-lysergic acid diethylamide (LSD) binding to recombinant

10 40 years, there is renewed interest in using lysergic acid diethylamide (LSD) in clinical psychiatric

11 Lysergic acid diethylamide (LSD) is a non-selective sero

12 Lysergic acid diethylamide (LSD) is the prototypical psy

13 ies have started to elucidate the effects of lysergic acid diethylamide (LSD) on the human brain but

14 -)-2,5-dimethoxy-4-iodoamphetamine (DOI) and lysergic acid diethylamide (LSD) stimulated a head-twitc

15 Using the ergoline lysergic acid diethylamide (LSD), and a series of substi

16 However, other 5-HT2A receptor ligands like lysergic acid diethylamide (LSD), in which the amine nit

17 nogens, including mescaline, psilocybin, and lysergic acid diethylamide (LSD), profoundly affect perc

18 The hallucinogen lysergic acid diethylamide (LSD; 0.1 mg/kg, i.p.) caused

19 ne (selective for the 5-HT2C receptor) and d-lysergic acid diethylamide (selective for the 5-HT2A rec

20 pressed high affinity binding sites for 125I-lysergic acid diethylamide and [3H]mesulergine.

21 Classic hallucinogens such as lysergic acid diethylamide are thought to elicit their p

22 significantly higher risk of dependence than lysergic acid diethylamide users.

23 ed the PLC-IP pathway, whereas others (e.g., lysergic acid diethylamide) favored the PLA2-AA pathway.

24 ted by 33% of the sample, most commonly LSD (lysergic acid diethylamide), amphetamines, Ecstasy (meth

25 emical studies showing that the hallucinogen lysergic acid diethylamide, its precursor ergotamine (ER

26 The hallucinogens studied [d-lysergic acid diethylamide, psilocin, bufotenin, and (+/

27 hallucinogenic drugs, such as psilocybin and lysergic acid diethylamide, require the 2AR and resemble

28 le compared with the prototypic hallucinogen lysergic acid diethylamide.

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

30 ds of recent other drug use (eg, cocaine and lysergic acid diethylamide; odds ratio [OR], 1.73; 95% C

31 HT(2A) receptor, a primary site of action of lysergic acid diethylamine (LSD), appears to dominate ef

32 ential validation of this model by utilizing lysergic acid dimethylamide (DAM-57), an ergot derivativ

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