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Mescaline and

Proposed Synthesis of MMDA and Mescaline by Rhodium and Osmium 980519... [Pg.172]

It is elear from these results that, in MDMA- or MBDB-trained rats, complete generalization of the training cue to the typical hallucinogenic drugs LSD, DOM, and mescaline does not occur. Furthermore, transfer of the training stimulus does not oecur to MDMA or MBDB in animals trained to diseriminate LSD from saline (Nichols et al. 1986). Although MDMA has been shown to substitute for mescaline (Callahan and Appel 1987). [Pg.8]

The answer is b. (Kn.lzu.ng, p 5.38.) Crack is the free-base (nonsalt) form of the alkaloid cocaine. It is called crack because, when heated, it makes a crackling sound. Heating crack enables a person to smoke it the drug is readily absorbed through the lungs and produces an intense euphoric effect in seconds Use has led to seizures and cardiac arrhythmias. Some of cocaine s effects (sympathomimetic) are due to blockade of norepinephrine reuptake into presynaptic terminals it does not block receptors. Flashbacks can occur with use of LSD and mescaline but have not been associated with the use of cocaine. [Pg.160]

Altura, B. T., and Altura, B. M. (1981) Phencyclidine, lysergic acid diethyl amide and mescaline Cerebral artery spasms and hallucinogenic activity. Science, 2 1051-1052. [Pg.23]

The possibility of cerebrovascular action of PCP was raised by the development of focal seizures and hemiparesis in a 6-year-old boy who had ingested what was presumed to be PCP (18). Hypertensive encephalopathy with a blood pressure of260/160 occurred in an 18-year-old woman who used PCP (43). These clinical findings are compatible with in vitro studies indicating that cerebral artery spasms can be produced by PCP as well as by LSD and mescaline (4). Whether such cerebrovascular actions are pertinent to the mental effects of these drugs is questionable. [Pg.144]

Bridger, W. H., and Mandel, I. J. (1967) The effects of dimethoxyphenylethylamine and mescaline on classical conditioning in rats as measured by the potentiated startle response. Life Sci., 6 775-781. [Pg.163]

As discussed, PCP, ditran, and scopolamine exert anticholinergic action. This property apparently is not linked to the hallucinogenic action of these molecules, however, since other hallucinogens, such as LSD and mescaline, do not affect cholinergic systems in doses sufficient to provoke hallucinatory-like behaviors in animals (67). Nevertheless, Revuelta et al. (96) noted a decreased turnover... [Pg.206]

The amphetamine and mescaline analogs which can be obtained by replacing carbon atoms with O, N, or S atoms may also be active, but little work has been done on this. For the synthesis of thienyl analogs see JACS 64,477(1942). [Pg.107]

Late 60 European LSD on sugar cubes and candy (left) and mescaline (right). [Pg.191]

Murray TF, Craigmill AL, Fischer GJ. (1977). Pharmacological and behavioral components of tolerance to LSD and mescaline in rats. Pharmacol Biochem Behav. 7(3) 239-44. [Pg.547]

Hallucinogenic activity Most classical" hallucinogens such as LSD and mescaline are antagonists at 5-HT2 receptors... [Pg.143]

An alkaloid is a complex organic chemical substance found in plants, which characteristically combines nitrogen with other elements, has a bitter taste, and typically has some toxic, stimulant, analgesic effects. There are many different alkaloids, 30 of which are found in the opium plant. While morphine is the most important alkaloid in opium—for its natural narcotic qualities as well as providing the chemical structure for heroin—another alkaloid, codeine, is also sought after for its medicinal attributes. Other alkaloids include papaverine, narcotine, nicotine, atropine, cocaine, and mescaline. While the concentration of morphine in opium varies depending on where and how the plant is cultivated, it typically ranges from 3 percent to 20 percent. [Pg.17]

Cross tolerance has been demonstrated between LSD and mescaline, psilocybin, and psilocin. There seems to be no cross tolerance between LSD and marijuana or amphetamine. These observations are indicative of the structural similarites of the compounds. [Pg.161]


See other pages where Mescaline and is mentioned: [Pg.1044]    [Pg.241]    [Pg.74]    [Pg.35]    [Pg.46]    [Pg.51]    [Pg.52]    [Pg.52]    [Pg.54]    [Pg.76]    [Pg.84]    [Pg.101]    [Pg.105]    [Pg.119]    [Pg.157]    [Pg.164]    [Pg.174]    [Pg.197]    [Pg.222]    [Pg.227]    [Pg.239]    [Pg.80]    [Pg.4]    [Pg.77]    [Pg.328]    [Pg.2]    [Pg.2]    [Pg.10]    [Pg.54]    [Pg.625]    [Pg.661]    [Pg.255]   
See also in sourсe #XX -- [ Pg.290 , Pg.291 , Pg.292 , Pg.293 ]

See also in sourсe #XX -- [ Pg.290 , Pg.291 , Pg.292 , Pg.293 ]




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Mescaline

Psilocybin and Mescaline

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