Results 151 to 160 of about 30,843 (202)
Some of the next articles are maybe not open access.
Clinical Toxicology, 1976
The results of the animal experiment demonstrate that oxidative hydroxylation is the major mode of metabolism of phencyclidine. It is evident that this process takes place in all three rings of the molecule. Hydroxylation of the piperidyl moiety probably also accounts for the formation of the N-dealkylated metabolites.
L K, Wong, K, Biemann
openaire +2 more sources
The results of the animal experiment demonstrate that oxidative hydroxylation is the major mode of metabolism of phencyclidine. It is evident that this process takes place in all three rings of the molecule. Hydroxylation of the piperidyl moiety probably also accounts for the formation of the N-dealkylated metabolites.
L K, Wong, K, Biemann
openaire +2 more sources
Phencyclidine and phenylcyclohexene disposition after smoking phencyclidine
Clinical Pharmacology and Therapeutics, 1982Five men who smoked parsley cigarettes containing 100 micrograms of [3H]-phencyclidine hydrochloride (PCP.HCl) inhaled 69 +/- 5(SEM) % of the total radioactivity in the cigarette. Both PCP and its pyrolysis product, 1-phenylcyclohexene (PC), were found and measured in plasma. Calculations based on the assumption that the ratio of these two products was
C E, Cook +4 more
openaire +2 more sources
2000
Abstract Phencyclidine (PCP) is an odorless, white, crystalline sub stance. Pure PCP has a MW of 243.9, a MP of 234°-236°C, and is highly insoluble in water. The most frequently encountered form of PCP is the hydrochloride salt, which has a MW of 279.9 and is soluble in both water and ethanol.
openaire +1 more source
Abstract Phencyclidine (PCP) is an odorless, white, crystalline sub stance. Pure PCP has a MW of 243.9, a MP of 234°-236°C, and is highly insoluble in water. The most frequently encountered form of PCP is the hydrochloride salt, which has a MW of 279.9 and is soluble in both water and ethanol.
openaire +1 more source