Effexor and other drugs like Tami-flu and Xanax (Larazapam) has 'angel dust' in it.
This is information from Dr. Fred Bell prior to his passing. It is
recorded in the archives of the bbsradio.com site.
PCP is well known for its primary action on
ionotropic
glutamate receptors, such as the
NMDA receptor in rats and in rat brain homogenate.[6][7]
As such, PCP is an NMDA receptor antagonist. NMDA receptors mediate
excitation,[8]
however, studies have shown that PCP unexpectedly produces substantial
cortical activation in humans[9]
and rodents.[10]
Research also indicates that PCP inhibits
nicotinic
acetylcholine (nACh) receptors. Analogues of PCP exhibit varying potency
at nACh receptors and NMDA receptors.[11]
In some brain regions, these effects are believed to act synergistically by
inhibiting excitatory activity.
PCP, like
ketamine,
also acts as a
D2 receptor
partial agonist in rat brain homogenate.[7]
This activity may be associated with some of the more psychotic features of
PCP intoxication, which is evidenced by the successful use of
D2 receptor antagonists (such as
haloperidol) in the treatment of PCP psychosis.[12]
The relative immunity to pain is likely produced by indirect interaction
with the endogenous
endorphin
and
enkephalin system, as has been suggested by studies involving rats.[13]
NOTE FROM DEE: People who take PCP have been known to fight
off 10 people without feeling any pain, and they are stronger throughout the
event than normal.
PCP may also work as a
dopamine reuptake inhibitor.[14]
Pharmacokinetics
PCP is metabolized into
PCHP,
PPC and PCAA.
When smoked, some of it is broken down by heat into
1-phenyl-1-cyclohexene (PC) and
piperidine.
Conversion of PCP into PC and piperidine by heat. (Image in
the PD)
Structural analogues
Possible Analogues of PCP
More than 30 different analogues of PCP were reported as being used on
the street during the 1970s and 1980s, mainly in the USA. The best known of
these are PCPy (rolicyclidine,
1-(1-phenylcyclohexyl)pyrrolidine); PCE (eticyclidine,
N-ethyl-1-phenylcyclohexylamine); and TCP (tenocyclidine,
1-(1-(2-Thienyl)cyclohexyl)piperidine). These compounds were never
widely-used and did not seem to be as well-accepted by users as PCP itself,
however they were all added onto Schedule I of the Controlled Substance Act
because of their putative similar effects.[15]
The generalized structural motif required for PCP-like activity is
derived from structure-activity relationship studies of PCP analogues, and
summarized below. All of these analogues would have somewhat similar effects
to PCP itself, although, with a range of potencies and varying mixtures of
anesthetic, dissociative and stimulant effects depending on the particular
substituents used. In some countries such as the USA, Australia, and New
Zealand, all of these compounds would be considered
controlled substance analogues of PCP, and are hence illegal drugs, even
though many of them have never been made or tested.[16][17]
Brain effects
Some studies found that, like other
NMDA receptor antagonists, phencyclidine can cause a certain kind of
brain damage called
Olney's lesions in rats.[18][19]
Studies conducted on rats showed that high doses of the NMDA receptor
antagonist
MK-801 caused reversible
vacuoles
to form in certain regions of the rats' brains. All studies of Olney's
lesions have only been performed on animals and may not apply to humans.
According to recent research, Olney's lesions only appear in the brains of
rodents. This is due to the fact that they lack a major metabolic enzyme
that is essential to breaking down NMDA receptor antagonists in the brain.
This enzyme is found in humans and makes humans essentially immune to
Olney's lesions as has been shown with ketamine.[20][21]
Phencyclidine has also been shown to cause
schizophrenia-like changes in N-acetylaspartate and N-acetylaspartylglutamate
in the rat brain, which are detectable both in living rats and upon necropsy
examination of brain tissue.[22]
It also induces symptoms in humans that mimic schizophrenia.[23]
The full extent of the pharmacology of this compound in the human CNS is
not fully understood; it binds to many different receptor sites. The primary
interactions are as a non-competitive antagonist at the 3A-subunit [epsilon
subunit] of the NMDA receptor. Phencyclidine is known to bind, with relatively high affinity, to the
D1 subunit of the human DAT (Dopamine Transporter), in
addition to displaying a positive antagonistic effect at the α7-subunit of
the Nicotinic Acetylcholine Receptor (nACh) It also binds to the mu-opioid receptor, which seems to be a central part of the mechanism of action
of drugs in this class. (For example, Dizocilpine [MK-801] shows little
appreciable analgesic effect despite having a high
specificity for the NMDA-3A and NMDA-3B subunits – this may well be mediated by the lack of related efficacy at
the mu-opioid receptor, though the NMDAR may play a role in transmission of pain signals).
History and
medicinal use
PCP was first synthesized in 1926 and later tested after
World War II as a surgical
anesthetic. Because of its adverse
side effects, such as
hallucinations,
mania,
delirium,
and
disorientation, it was shelved until the 1950s. In 1953, it was patented
by
Parke-Davis and named Sernyl (referring to serenity),[24]
but was only used in humans for a few years because of side-effects. In
1967, it was given the
trade
name Sernylan and marketed as a
veterinary anesthetic, but was again discontinued. Its side effects and
long
half-life in the human body made it unsuitable for medical applications.
Recreational uses
Illicit PCP seized by the DEA in several forms.
PCP began to emerge as a
recreational drug in major cities in the
United States in 1967.[25]
In 1978,
People magazine and
Mike Wallace of
60
Minutes called PCP the country's "number one" drug problem. Although
recreational use of the drug had always been relatively low, it began
declining significantly in the 1980s. In surveys, the number of
high
school students admitting to trying PCP at least once fell from 13% in
1979 to less than 3% in 1990.[26]
PCP comes in both powder and liquid forms (PCP base is dissolved most
often in
ether), but typically it is sprayed onto leafy material such as
cannabis,
mint,
oregano,
parsley,
or ginger
leaves, then smoked.
PCP is a
Schedule II substance in the United States, a Schedule I drug by the
Controlled Drugs and Substances act in Canada, a List I drug of the
Opium Law
in the
Netherlands and a
Class A substance in the United Kingdom.
Methods of
administration
In its pure (free
base) form, PCP is a yellow oil (usually dissolved in
petroleum,
diethyl ether, or
tetrahydrofuran). Upon treatment with
hydrogen chloride gas, or
isopropyl alcohol saturated with
hydrochloric acid, this oil precipitates into white-tan crystals or
powder (PCP hydrochloride). In this, the
salt form, PCP can be
insufflated, depending upon the purity. However, most PCP on the illicit
market often contains a number of
contaminants as a result of makeshift manufacturing, causing the color
to range from tan to brown, and the consistency to range from powder to a
gummy mass. These contaminants can range from unreacted
piperidine and other
precursors, to
carcinogens like
benzene
and cyanide-like
compounds such as PCC (piperidinocyclohexyl carbonitrile).
The term "embalming fluid" is often used to refer to the liquid PCP in
which a cigarette is dipped, to be ingested through smoking, commonly known
as "boat" or "water." The name most likely originated from the somatic
"numbing" effect and feelings of
dissociation induced by PCP, and has led to the widespread and
mistaken belief that the liquid is made up of or contains real
embalming fluid. Occasionally, however, some users and dealers could
have, believing this myth, used real embalming fluid mixed with, or in place
of, PCP.[27][28]
Smoking PCP is known as "getting wet", and a
cigarette
or
joint which has been dipped in PCP may be referred to on the street as a
"fry stick," "sherm," "leak," "amp," "lovely," "KJ (an abbreviation for
'Killer Joint')," "toe tag", "dipper", "happy stick," or "wet stick."
"Getting wet" may have once been a popular method of using PCP, especially
in the
western United States where it may have been sold for about $10 to $25
per cigarette.
Effects
Behavioral effects can vary by dosage. Low doses produce a numbness in
the extremities and intoxication, characterized by staggering, unsteady
gait, slurred speech, bloodshot eyes, and loss of balance. Moderate doses
(5–10 mg intranasal, or 0.01–0.02 mg/kg intramuscular or intravenous) will
produce
analgesia and
anesthesia. High doses may lead to
convulsions.[29]
Users frequently do not know how much of the drug they are taking due to the
tendency of the drug to be made illegally in uncontrolled conditions.[30]
Psychological effects include severe changes in
body
image,
loss of
ego boundaries,
paranoia
and
depersonalization.
Hallucinations,
euphoria,
suicidal impulses and aggressive behavior are reported.[29][31]
The drug has been known to alter mood states in an unpredictable fashion,
causing some individuals to become detached, and others to become animated.
Intoxicated individuals may act in an unpredictable fashion, possibly driven
by their delusions and hallucinations. PCP may induce feelings of strength,
power, and invulnerability as well as a numbing effect on the mind.[5]
Occasionally, this leads to bizarre acts of violence, such as in the case of
Big Lurch,
a former rapper who claimed his room mate was the devil and ate part of her
lung.
[32]
However, studies by the
Drug Abuse Warning Network in the 1970s show that media reports of
PCP-induced violence are greatly exaggerated and that incidents of violence
were unusual and often (but not always) limited to individuals with
reputations for aggression regardless of drug use.[33]
The reports in question often dealt with a supposed increase in strength
imparted by the drug; this could partially be explained by the anaesthetic
effects of the drug. The most commonly-cited types of incidents included
self-mutilation of various types, breaking handcuffs (a feat reportedly
requiring about 10,000 lbs of force to break a stainless steel chain of
typical diameter), inflicting remarkable property damage, and pulling one's
own teeth.[33][34][32]
Included in the portfolio of behavioral disturbances are acts of
self-injury including suicide, and attacks on others or destruction of
property. The analgesic properties of the drug can cause users to feel less
pain, and persist in violent or injurious acts as a result. Recreational
doses of the drug can also induce a psychotic state that resembles
schizophrenic episodes which can last for months at a time with toxic doses.[35]
Users generally report they feel detached from reality, or that one's
consciousness seems somewhat disconnected from reality.[36]
Symptoms are summarized by the
mnemonic
device RED DANES: rage,
erythema
(redness of skin), dilated pupils, delusions,
amnesia,
nystagmus
(oscillation of the eyeball when moving laterally), excitation, and skin
dryness.[37]
Management of
intoxication
Management of phencyclidine intoxication mostly consists of supportive
care — controlling breathing, circulation, and body temperature — and, in
the early stages, treating psychiatric symptoms.[38][39][40]
Benzodiazepines, such as
lorazepam,
are the
drugs of choice to control agitation and seizures (when present).
Typical antipsychotics such as
phenothiazines and
haloperidol have been used to control psychotic symptoms, but may
produce many undesirable side effects — such as
dystonia
— and their use is therefore no longer preferred; phenothiazines are
particularly risky, as they may lower the
seizure threshold, worsen
hyperthermia, and boost the
anticholinergic effects of PCP.[38][39]
If an antipsychotic is given,
intramuscular haloperidol has been recommended.[40][41][42]
Forced acid diuresis (with
ammonium chloride or, more safely,
ascorbic acid) may increase clearance of PCP from the body, and was
somewhat controversially recommended in the past as a
decontamination measure.[38][39][40]
However, it is now known that only around 10% of a dose of PCP is removed by
the kidneys, which would make increased urinary clearance of little
consequence; furthermore, urinary
acidification
is dangerous, as it may induce
acidosis
and worsen
rhabdomyolysis (muscle breakdown), which is not an unusual manifestation
of PCP toxicity.[38][39]
See also
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- Notes
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-
TCB-2
-
TFMFly
-
TMA
Piperazines:
pFPP
-
TMFPP
Tryptamines:
1-Methyl-5-methoxy-diisopropyltryptamine
-
2,N,N-TMT
-
4,N,N-TMT
-
4-HO-5-MeO-DMT
-
4-Acetoxy-DET
-
4-Acetoxy-DIPT
-
4-Acetoxy-DMT
-
4-Acetoxy-DPT
-
4-Acetoxy-MiPT
-
4-HO-DPT
-
4-HO-MET
-
4-Propionyloxy-DMT
-
4-HO-MPMI
-
5-Me-MIPT
-
5-N,N-TMT
-
5-AcO-DMT
-
5-MeO-2,N,N-TMT
-
5-MeO-4,N,N-TMT
-
5-MeO-α,N,N-TMT
-
5-MeO-α-ET
-
5-MeO-α-MT
-
5-MeO-DALT
-
5-MeO-DET
-
5-MeO-DIPT
-
5-MeO-DMT
-
5-MeO-DPT
-
5-MeO-EiPT
-
5-MeO-MET
-
5-MeO-MIPT
-
5-MeO-MPMI
-
7,N,N-TMT
-
α,N,N-TMT
-
α-ET
-
α-MT
-
AL-37350A
-
Baeocystin
-
Bufotenin
-
DALT
-
DBT
-
DCPT
-
DET
-
DIPT
-
DMT
-
DPT
-
EiPT
-
Ethocin
-
Ethocybin
-
Iprocin
-
MET
-
Miprocin
-
MIPT
-
Norbaeocystin
-
PiPT
-
Psilocin
-
Psilocybin
Others:
AL-38022A
-
Elemicin
-
Ibogaine
-
Myristicin
-
Noribogaine
-
Voacangine
|
|
Dissociatives
NMDAR
antagonists |
|
|
Deliriants
mAChR
antagonists |
|
|
Miscellaneous |
|
|
[show]
|
|
Adamantanes |
|
|
Adenosine antagonists |
|
|
Alkylamines |
|
|
Arylcyclohexylamines |
|
|
Benzazepines |
|
|
Cholinergics |
|
|
Convulsants |
|
|
Eugeroics |
|
|
Oxazolines |
|
|
Phenethylamines |
-
1-(4-Methylphenyl)-2-aminobutane
-
1-Phenyl-2-(piperidin-1-yl)pentan-3-one
-
1-Methylamino-1-(3,4-methylenedioxyphenyl)propane
-
2-Fluoroamphetamine
-
2-Fluoromethamphetamine
-
2-OH-PEA
-
2-Phenyl-3-aminobutane
-
2-Phenyl-3-methylaminobutane
-
2,3-MDA
-
3-Fluoroamphetamine
-
3-Fluoroethamphetamine
-
3-Fluoromethcathinone
-
3-Methoxyamphetamine
-
3-Methylamphetamine
-
3,4-DMMC
-
4-BMC
-
4-Ethylamphetamine
-
4-FA
-
4-FMA
-
4-MA
-
4-MMA
-
4-MTA
-
6-FNE
-
AL-1095
-
Alfetamine
-
a-Ethylphenethylamine
-
Amfecloral
-
Amfepentorex
-
Amfepramone
-
Amidephrine
-
2-Amino-1,2-dihydronaphthalene
-
2-Aminoindane
-
5-(2-Aminopropyl)indole
-
2-Aminotetralin
-
Amphetamine (Dextroamphetamine,
Levoamphetamine)
-
Amphetaminil
-
Arbutamine
-
ß-Methylphenethylamine
-
ß-Phenylmethamphetamine
-
Benfluorex
-
Benzedrone
-
Benzphetamine
-
BDB
-
BOH
-
3-Benzhydrylmorpholine
-
BPAP
-
Buphedrone
-
Bupropion
-
Butylone
-
Camfetamine
-
Cathine
-
Cathinone
-
Chlorphentermine
-
Cilobamine
-
Cinnamedrine
-
Clenbuterol
-
Clobenzorex
-
Cloforex
-
Clortermine
-
Cypenamine
-
D-Deprenyl
-
Denopamine
-
Dimethoxyamphetamine
-
Dimethylamphetamine
-
Dimethylcathinone
-
Dobutamine
-
DOPA (Dextrodopa,
Levodopa)
-
Dopamine
-
Dopexamine
-
Droxidopa
-
EBDB
-
Ephedrine
-
Epinephrine
-
Epinine
-
Etafedrine
-
Ethcathinone
-
Ethylamphetamine
-
Ethylnorepinephrine
-
Ethylone
-
Etilefrine
-
Famprofazone
-
Fenbutrazate
-
Fencamfamine
-
Fencamine
-
Fenethylline
-
Fenfluramine (Dexfenfluramine,
Levofenfluramine)
-
Fenmetramide
-
Fenproporex
-
Feprosidnine
-
Flephedrone
-
Fludorex
-
Furfenorex
-
G-130
-
Gepefrine
-
Hexapradol
-
HMMA
-
Hordenine
-
Hydroxyamphetamine
-
5-Iodo-2-aminoindane
-
Ibopamine
-
IMP
-
Indanylamphetamine
-
Iofetamine
-
Isoetarine
-
Isoethcathinone
-
Isoprenaline
-
L-Deprenyl (Selegiline)
-
Lefetamine
-
Lisdexamfetamine
-
Lophophine
-
Manifaxine
-
MBDB
-
MDA
-
MDBU
-
MDEA
-
MDMA
-
MDMPEA
-
MDOH
-
MDPR
-
MDPEA
-
Mefenorex
-
Mephedrone
-
Mephentermine
-
Metanephrine
-
Metaraminol
-
Mesocarb
-
Methamphetamine (Dextromethamphetamine,
Levomethamphetamine)
-
Methoxamine
-
Methoxyphenamine
-
MMA
-
Methcathinone
-
Methedrone
-
Methoxyphenamine
-
Methylone
-
MMDA
-
MMDMA
-
MMMA
-
Morazone
-
N-Benzyl-1-phenethylamine
-
N,N-Dimethylphenethylamine
-
Naphthylamphetamine
-
Nisoxetine
-
Norepinephrine
-
Norfenefrine
-
Norfenfluramine
-
Normetanephrine
-
L-Norpseudoephedrine
-
Octopamine
-
Orciprenaline
-
Ortetamine
-
Oxilofrine
-
PBA
-
PCA
-
PHA
-
Pargyline
-
Pentorex
-
Pentylone
-
Phenatine
-
Phendimetrazine
-
Phenmetrazine
-
Phenpromethamine
-
Phentermine
-
Phenylalanine
-
2-Phenyl-3,6-dimethylmorpholine
-
Phenylephrine
-
Phenylpropanolamine
-
Pholedrine
-
PIA
-
PMA
-
PMEA
-
PMMA
-
PPAP
-
Phthalimidopropiophenone
-
Prenylamine
-
Propylamphetamine
-
Pseudoephedrine
-
Pseudophenmetrazine
-
Radafaxine
-
Ropinirole
-
Salbutamol (Levosalbutamol)
-
Sibutramine
-
Synephrine
-
Theodrenaline
-
Tiflorex
-
Tranylcypromine
-
Tyramine
-
Tyrosine
-
Xylopropamine
-
Zylofuramine
|
|
Piperazines |
|
|
Piperidines |
|
|
Pyrrolidines |
|
|
Tropanes |
|
|
Others |
|
|
|
|
|
|
|
|
|
- Agonists:
77-LH-28-1
-
AC-42
-
AC-260,584
-
Aceclidine
-
Acetylcholine
-
AF30
-
AF150(S)
-
AF267B
-
AFDX-384
-
Alvameline
-
AQRA-741
-
Arecoline
-
Bethanechol
-
Butyrylcholine
-
Carbachol
-
CDD-0034
-
CDD-0078
-
CDD-0097
-
CDD-0098
-
CDD-0102
-
Cevimeline
-
Choline
-
cis-Dioxolane
-
Ethoxysebacylcholine
-
LY-593,039
-
L-689,660
-
LY-2,033,298
-
McNA343
-
Methacholine
-
Milameline
-
Muscarine
-
NGX-267
-
Ocvimeline
-
Oxotremorine
-
PD-151,832
-
Pilocarpine
-
RS86
-
Sabcomeline
-
SDZ 210-086
-
Sebacylcholine
-
Suberylcholine
-
Talsaclidine
-
Tazomeline
-
Thiopilocarpine
-
Vedaclidine
-
VU-0029767
-
VU-0090157
-
VU-0152099
-
VU-0152100
-
VU-0238429
-
WAY-132,983
-
Xanomeline
-
YM-796
Antagonists:
3-Quinuclidinyl Benzilate
-
4-DAMP
-
Aclidinium Bromide
-
Anisodamine
-
Anisodine
-
Atropine
-
Atropine Methonitrate
-
Benactyzine
-
Benzatropine/Benztropine
-
Benzydamine
-
BIBN 99
-
Biperiden
-
Bornaprine
-
CAR-226,086
-
CAR-301,060
-
CAR-302,196
-
CAR-302,282
-
CAR-302,368
-
CAR-302,537
-
CAR-302,668
-
CS-27349
-
Cyclobenzaprine
-
Cyclopentolate
-
Darifenacin
-
DAU-5884
-
Dimethindene
-
Dexetimide
-
DIBD
-
Dicyclomine/Dicycloverine
-
Ditran
-
EA-3167
-
EA-3443
-
EA-3580
-
EA-3834
-
Etanautine
-
Etybenzatropine/Ethylbenztropine
-
Flavoxate
-
Himbacine
-
HL-031,120
-
Ipratropium bromide
-
J-104,129
-
Hyoscyamine
-
Mamba Toxin 3
-
Mamba Toxin 7
-
Mazaticol
-
Mebeverine
-
Methoctramine
-
Metixene
-
N-Ethyl-3-Piperidyl Benzilate
-
N-Methyl-3-Piperidyl
Benzilate
-
Orphenadrine
-
Otenzepad
-
Oxybutynin
-
PBID
-
PD-102,807
-
PD-0298029
-
Phenglutarimide
-
Phenyltoloxamine
-
Pirenzepine
-
Piroheptine
-
Procyclidine
-
Profenamine
-
RU-47,213
-
SCH-57,790
-
SCH-72,788
-
SCH-217,443
-
Scopolamine/Hyoscine
-
Solifenacin
-
Telenzepine
-
Tiotropium bromide
-
Tolterodine
-
Trihexyphenidyl
-
Tripitamine
-
Tropatepine
-
Tropicamide
-
WIN-2299
-
Xanomeline
-
Zamifenacin; Others:
1st Generation Antihistamines (Brompheniramine
-
chlorphenamine
-
cyproheptadine
-
dimenhydrinate
-
diphenhydramine
-
doxylamine
-
mepyramine/pyrilamine
-
phenindamine
-
pheniramine
-
tripelennamine
-
triprolidine, etc)
-
Tricyclic Antidepressants (Amitriptyline
-
doxepin
-
trimipramine, etc)
-
Tetracyclic Antidepressants (Amoxapine
-
maprotiline, etc)
-
Typical Antipsychotics (Chlorpromazine
-
thioridazine, etc)
-
Atypical Antipsychotics (Clozapine
-
olanzapine
-
quetiapine, etc)
|
|
|
- Agonists:
5-HIAA
-
A-84,543
-
A-366,833
-
A-582,941
-
A-867,744
-
ABT-202
-
ABT-418
-
ABT-560
-
ABT-894
-
Acetylcholine
-
Altinicline
-
Anabasine
-
Anatoxin-a
-
AR-R17779
-
Butinoline
-
Butyrylcholine
-
Carbachol
-
Choline
-
Cotinine
-
Cytisine
-
Decamethonium
-
Desformylflustrabromine
-
Dianicline
-
Dimethylphenylpiperazinium
-
Epibatidine
-
Epiboxidine
-
Ethanol
-
Ethoxysebacylcholine
-
EVP-4473
-
EVP-6124
-
Galantamine
-
GTS-21
-
Ispronicline
-
Lobeline
-
MEM-63,908/RG-3487
-
Nicotine
-
NS-1738
-
PHA-543,613
-
PHA-709,829
-
PNU-120,596
-
PNU-282,987
-
Pozanicline
-
Rivanicline
-
RJR-2429
-
Sazetidine A
-
Sebacylcholine
-
SIB-1508Y
-
SIB-1553A
-
SSR-180,711
-
Suberylcholine
-
Suxamethonium/Succinylcholine
-
TC-1698
-
TC-1734
-
TC-1827
-
TC-2216
-
TC-5214
-
TC-5619
-
TC-6683
-
Tebanicline
-
Tropisetron
-
UB-165
-
Varenicline
-
WAY-317,538
-
XY-4083
Antagonists:
18-Methoxycoronaridine
-
α-Bungarotoxin
-
α-Conotoxin
-
Alcuronium
-
Amantadine
-
Anatruxonium
-
Atracurium
-
Bupropion
-
Chandonium
-
Chlorisondamine
-
Cisatracurium
-
Coclaurine
-
Coronaridine
-
Dacuronium
-
Decamethonium
-
Dextromethorphan
-
Dextropropoxyphene
-
Dextrorphan
-
Diadonium
-
DHβE
-
Dimethyltubocurarine/Metocurine
-
Dipyrandium
-
Dizocilpine/MK-801
-
Doxacurium
-
Duador
-
Esketamine
-
Fazadinium
-
Gallamine
-
Hexafluronium
-
Hexamethonium/Benzohexonium
-
Ibogaine
-
Isoflurane
-
Ketamine
-
Kynurenic acid
-
Laudexium/Laudolissin
-
Levacetylmethadol
-
Malouetine
-
Mecamylamine
-
Memantine
-
Methadone (Levomethadone)
-
Methorphan/Racemethorphan
-
Methyllycaconitine
-
Metocurine
-
Mivacurium
-
Morphanol/Racemorphan
-
Neramexane
-
Nitrous Oxide
-
Pancuronium
-
Pempidine
-
Pentamine
-
Pentolinium
-
Phencyclidine
-
Pipecuronium
-
Radafaxine
-
Rapacuronium
-
Rocuronium
-
Surugatoxin
-
Thiocolchicoside
-
Toxiferine
-
Trimethaphan
-
Tropeinium
-
Tubocurarine
-
Vecuronium
-
Xenon
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
-
Cymserine * Many
of the acetylcholinesterase
inhibitors listed above act
as butyrylcholinesterase
inhibitors.
|
|
|
|
|
|
|
|
|
|
|
|
- Adamantanes:
Amantadine
-
Memantine
-
Rimantadine; Aminotetralins:
7-OH-DPAT
-
8-OH-PBZI
-
Rotigotine
-
UH-232; Benzazepines:
6-Br-APB
-
Fenoldopam
-
SKF-38,393
-
SKF-77,434
-
SKF-81,297
-
SKF-82,958
-
SKF-83,959; Ergolines:
Bromocriptine
-
Cabergoline
-
Dihydroergocryptine
-
Epicriptine
-
Lisuride
-
LSD
-
Pergolide; Dihydrexidine
derivatives:
2-OH-NPA
-
A-86,929
-
Ciladopa
-
Dihydrexidine
-
Dinapsoline
-
Dinoxyline
-
Doxanthrine; Others:
A-68,930
-
A-77636
-
A-412,997
-
ABT-670
-
ABT-724
-
Aplindore
-
Apomorphine
-
Aripiprazole
-
Bifeprunox
-
BP-897
-
CY-208,243
-
Dizocilpine
-
Etilevodopa
-
Flibanserin
-
Ketamine
-
Melevodopa
-
Modafinil
-
Pardoprunox
-
Phencyclidine
-
PD-128,907
-
PD-168,077
-
PF-219,061
-
Piribedil
-
Pramipexole
-
Propylnorapomorphine
-
Pukateine
-
Quinagolide
-
Quinelorane
-
Quinpirole
-
RDS-127
-
Ro10-5824
-
Ropinirole
-
Rotigotine
-
Roxindole
-
Salvinorin A
-
SKF-89,145
-
Sumanirole
-
Terguride
-
Umespirone
-
WAY-100,635
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Ionotropic |
|
|
|
|
- Agonists: Glutamate/acite site
competitive agonists:
Aspartate
-
Glutamate
-
Homoquinolinic acid
-
Ibotenic acid
-
NMDA
-
Quinolinic acid
-
Tetrazolylglycine; Glycine site
agonists:
ACBD
-
ACPC
-
ACPD
-
Alanine
-
CCG
-
Cycloserine
-
DHPG
-
Fluoroalanine
-
Glycine
-
HA-966
-
L-687,414
-
Milacemide
-
Sarcosine
-
Serine
-
Tetrazolylglycine; Polyamine site
agonists:
Acamprosate
-
Spermidine
-
Spermine
Antagonists: Competitive
antagonists:
AP5 (APV)
-
AP7
-
CGP-37849
-
CGP-39551
-
CGP-39653
-
CGP-40116
-
CGS-19755
-
CPP
-
LY-233,053
-
LY-235,959
-
LY-274,614
-
MDL-100,453
-
Midafotel (d-CPPene)
-
NPC-12,626
-
NPC-17,742
-
PBPD
-
PEAQX
-
Perzinfotel
-
PPDA
-
SDZ-220581
-
Selfotel; Noncompetitive antagonists:
ARR-15,896
-
Caroverine
-
Dexanabinol
-
FPL-12495
-
FR-115,427
-
Hodgkinsine
-
Magnesium
-
MDL-27,266
-
NPS-1506
-
Psychotridine
-
Zinc; Uncompetitive pore blockers:
2-MDP
-
3-MeO-PCP
-
8A-PDHQ
-
Alaproclate
-
Amantadine
-
Aptiganel
-
ARL-12,495
-
ARL-15,896-AR
-
ARL-16,247
-
Budipine
-
Delucemine
-
Dexoxadrol
-
Dextrallorphan
-
Dieticyclidine
-
Dizocilpine
-
Endopsychosin
-
Esketamine
-
Etoxadrol
-
Eticyclidine
-
Gacyclidine
-
Ibogaine
-
Indantadol
-
Ketamine
-
Ketobemidone
-
Loperamide
-
Memantine
-
Meperidine (Pethidine)
-
Methadone (Levomethadone)
-
Methorphan (Dextromethorphan
-
Levomethorphan)
-
Methoxetamine
-
Milnacipran
-
Morphanol (Dextrorphan
-
Levorphanol)
-
NEFA
-
Neramexane
-
Nitrous oxide
-
Noribogaine
-
Orphenadrine
-
PCPr
-
Phencyclamine
- Phencyclidine
-
Propoxyphene
-
Remacemide
-
Rhynchophylline
-
Riluzole
-
Rimantadine
-
Rolicyclidine
-
Sabeluzole
-
Tenocyclidine
-
Tiletamine
-
Tramadol
-
Xenon; Glycine site antagonists:
ACEA-1021
-
ACEA-1328
-
ACPC
-
Carisoprodol
-
CGP-39653
-
CKA
-
DCKA
-
Felbamate
-
Gavestinel
-
GV-196,771
-
Kynurenic acid
-
L-689,560
-
L-701,324
-
Lacosamide
-
Licostinel
-
LU-73,068
-
MDL-105,519
-
Meprobamate
-
MRZ 2/576
-
PNQX
-
ZD-9379; NR2B subunit antagonists:
Besonprodil
-
CO-101,244 (PD-174,494)
-
CP-101,606
-
Eliprodil
-
Haloperidol
-
Ifenprodil
-
Isoxsuprine
-
Nylidrin
-
Ro8-4304
-
Ro25-6981
-
Traxoprodil; Polyamine site
antagonists:
Arcaine
-
Co 101676
-
Diaminopropane
-
Acamprosate
-
Diethylenetriamine
-
Huperzine A
-
Putrescine
-
Ro 25-6981; Unclassified/unsorted
antagonists:
Chloroform
-
Diethyl ether
-
Enflurane
-
Ethanol (Alcohol)
-
Halothane
-
Isoflurane
-
Methoxyflurane
-
Toluene
-
Trichloroethane
-
Trichloroethanol
-
Trichloroethylene
-
Xylene
|
|
|
|
|
|
Metabotropic |
|
|
Transporter
inhibitors |
|
|
Others |
|
|
Receptor
Ligands
Agonists
3-PPP
4-IBP
4-PPBP
Afobazole
AllylnormetazocineAmitriptyline
Amphetamine
Berberine
Citalopram
Clorgyline
Cocaine
Cyclazocine
Dextrallorphan
Dextromethorphan
Dextrorphan
DTG
BD-1,008
Desipramine
DHEA
Dimethyltryptamine
Dimemorfan
Ditolylguanidine
EMD-57,445
Escitalopram
Fluoxetine
Fluvoxamine
Heroin
Igmesine
Imipramine
JO-1,784
L-687,384
Lamotrigine
Lu 28-179
MDMA
Methamphetamine
Morphine
Naluzotan
Noscapine
OPC-14,523
Opipramol
PB-28
PD-144,415
Pentazocine
Pentoxyverine
Phencyclidine
PRE-084
Pregnenolone
RTI-55
SA-4503
Sertraline
Siramesine
Venlafaxine
Antagonists
BD-1,047
BD-1,063
BMY-14,802
E-5,842
Haloperidol
NE-100
Progesterone
Rimcazole
SM-21
Unknown
Clocapramine
Gevotroline
HERE IS MORE PROOF:
http://search.aol.com/aol/search?q=Phencyclidine&s_it=spelling&v_t=wscreen-smallbusiness-w
www.greatdreams.com/drugs.htm
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Undo
Mar 11, 2010 –
ecstasy, heroin, opium, methamphetamines, LSD, psylocibin, peyote, PCP,
amphetamines, uppers and downers. Some are happy about their ...
HERE ARE MORE ATICLES ABOUT DRUGS AND THEIR USE
http://www.google.com/#sclient=psy-ab&hl=en&rlz=1R2ACGW_enUS361&q=site:greatdreams.com++DRUGS&rlz=1R2ACGW_enUS361&oq=site:greatdreams.com++DRUGS&gs_l=hp.3...60198.63319.1.64308.8.8.0.0.0.0.355.2145.2-6j2.8.0.les%3B..0.0...1c.1.V5KyYw2YhO4&pbx=1&bav=on.2,or.r_gc.r_pw.&fp=ae4598fbef7967ce&biw=1280&bih=754