Torez's profile

August 18th, 2006
January 5th, 2015
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?Walken Evens The Score 3,171 32 (3.94)  2011-03-20
?Tommy Gavin makes it Baked 1,821 9 (3.89)  2010-10-17
?(nsfw) Isn't it beautiful? 1,539 9 (3.11)  2010-10-10
?Tommy Gavin makes it rain 2,750 30 (3.93)  2010-10-10
?Yolanda Won't Shut Up 13,035 127 (4.31)  2010-09-12

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?Humanity™ 21,192 191 (4.43)  2010-09-11
?Yolanda Won't Shut Up 13,035 127 (4.31)  2010-09-12
?(nsfw) Nigga Stole The Wrong Guy's Bike (... 20,307 496 (3.97)  2007-06-30
?Nintendo fan says brb FBI 14,868 421 (3.96)  2006-08-18
?Walken Evens The Score 3,171 32 (3.94)  2011-03-20

recent comments

February 27th, 2011
Winception
November 14th, 2010
I'll bite...Your bag and everything else
October 24th, 2010
On on the site ?My cat on PcP
Phencyclidine
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This article needs attention from an expert on the subject. See the talk page for details. WikiProject Pharmacology or the Pharmacology Portal may be able to help recruit an expert. (January 2010)
Phencyclidine
Systematic (IUPAC) name
1-(1-phenylcyclohexyl)piperidine
Identifiers
CAS number 77-10-1
ATC code None
PubChem CID 6468
DrugBank DB03575
ChemSpider 6224
Chemical data
Formula C17H25N
Mol. mass 243.387 g/mol
Pharmacokinetic data
Half-life 7-46 hours
Therapeutic considerations
Pregnancy cat. ?
Legal status Schedule I (CA) ? (UK) Schedule II (US)
Routes Smoked, Insufflated, Oral
YesY(what is this?) (verify)

Phencyclidine (a complex clip of the chemical name 1-(1-phenylcyclohexyl)piperidine, commonly initialized as PCP), also known as angel dust and other street names, is a recreational, dissociative drug formerly used as an anesthetic agent, exhibiting hallucinogenic and neurotoxic effects.[1] Developed in 1926,[2] it was first patented in 1952 by the Parke-Davis pharmaceutical company and marketed under the brand name Sernyl. In chemical structure, PCP is an arylcyclohexylamine derivative, and, in pharmacology, it is a member of the family of dissociative anesthetics. PCP works primarily as an NMDA receptor antagonist, which blocks the activity of the NMDA receptor and, like most antiglutamatergic hallucinogens, is significantly more dangerous than other categories of hallucinogens.[3][4] Other NMDA receptor antagonists include ketamine, tiletamine, and dextromethorphan. Although the primary psychoactive effects of the drug lasts for a few hours, the total elimination rate from the body typically extends eight days or longer.
Contents
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* 1 Biochemistry and pharmacology
o 1
October 24th, 2010
On on the site ?Go! Bwaaah!
Funny site. Bwaaah!