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Synthetic Drug Compound Table

Synthetic marijuana and synthetic cocaine, commonly known as “bath salts,” are comprised of compounds created in laboratories, often for scientific research or medicinal purposes, and repurposed for recreational use.

Some of these compounds were created decades ago and then forgotten about until recently when they were re-discovered by a new generation and put to use as recreational drugs.

This is a list of some of those synthetic compounds. Most of them are synthetic cannabinoids, meaning they react with the body’s two known cannabinoid receptors, which are the cells in your body that interact with the THC in marijuana to produce a “high” feeling. Some of the compounds on the list are synthetic stimulants similar to methamphetamine or cocaine. Not all of these compounds have been found in synthetic drugs and this list is not meant to be definitive, as new compounds are constantly being discovered or used in ways they were not intended for.

Each compound is listed under its most common name, along with other names it’s known by and some information about it, including if it has been found as an ingredient in synthetic drugs and if it is illegal or banned anywhere.

Again, it is not meant to be a definitive list, just a resource for people wanting to know the scope of synthetic substances that are available for potential abuse.

Drug Compound

Info

1-Butyl-3-(2-methoxybenzoyl)indole

A benzoylindole type synthetic cannabinoid.

1-Butyl-3-(4-methoxybenzoyl)indole

A benzoylindole type synthetic cannabinoid.

1-Pentyl-3-(2-methoxybenzoyl)indole

A benzoylindole type synthetic cannabinoid.

2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene

An analgesic compound which is a cannabinoid agonist.

3,4-Dimethylmethcathinone

Aka 3,4-DMMC, it is a stimulant drug first reported in 2010 as a designer drug analogue of mephedrone, apparently produced in response to the banning of mephedrone. It is illegal in some places.

5-Fluoropentyl-3-pyridinoylindole

A synthetic cannabinoid receptor agonist that has been found in synthetic marijuana smoking blends.

5F-PB-22

A synthetic cannabinoid receptor agonist that has been found in synthetic marijuana smoking blends.

9-nor-9β-Hydroxyhexahydrocannabinol

Aka HHC, it is a synthetic cannabinoid derivative which resulted from early modifications to the structure of THC. An obscure derivative (C8)-CP 47,497 was found to have been sold as the active ingredient in the synthetic marijuana product Spice.

A-40174

Aka SP-1, it is an analgesic drug which acts as a potent cannabinoid receptor agonist.

A-41988

Aka BW29Y, it is an analgesic drug which acts as a cannabinoid agonist.

A-42574

A classical synthetic cannabinoid.

A-796,260

A drug that acts as a potent and selective cannabinoid CB2 receptor agonist.

A-834,735

A drug that acts as a potent cannabinoid receptor full agonist at both the CB1 and CB2 receptors.

A-836,339

A drug that acts as a potent cannabinoid receptor full agonist. It is selective for CB2.

A-955,840

A synthetic cannabinoid receptor agonist.

AB-001

Aka 1-pentyl-3-(1-adamantoyl)indole, it is a designer drug that was found as an ingredient in synthetic cannabis smoking blends.

AB-005

Chemical name; [1-[(1-methyl-2-piperidinyl)methyl]-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-methanone, it is a designer drug offered by online vendors as a cannabimimetic agent.

AB-FUBINACA

A drug that acts as a potent agonist for the cannabinoid receptors. It has been identified as an ingredient in synthetic marijuana smoking products.

Abnormal cannabidiol

A synthetic regioisomer of cannabidiol, which unlike most other cannabinoids produces vasodilator effects, lowers blood pressure, and induces cell migration, cell proliferation and mitogen-activated protein kinase activation in microglia, but without producing any psychoactive effects.

AB-PINACA

A compound that has been identified as a component of synthetic marijuana products.

ACEA

A synthetic cannabinoid receptor agonist from the eicosanoid family.

ACPA

A synthetic cannabinoid receptor agonist from the eicosanoid family.

ADB-FUBINACA

A designer drug identified in synthetic marijuana blends.

ADBICA

A designer drug identified in synthetic marijuana blends.

AKB48

Aka APINACA, it is a drug that acts as a reasonably potent agonist for the cannabinoid receptors and has been identified as an ingredient in synthetic marijuana smoking blends. It is illegal in some countries.

AM-087

An analgesic CB1 agonist around 100x more potent than THC itself.

AM-251

An inverse agonist at the CB1 cannabinoid receptor.

AM-281

N-(morpholin-4-yl)-1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-1H-pyrazole-3-carboxamide

AM-356

Aka Methanandamide, it is a synthetically created stable chiral analog of anandamide and its effects have been observed to act on the cannabinoid receptors, specifically on CB1 receptors.

AM-374

Also known as palmitylsulfonyl fluoride.

AM-381

Also known as stearylsulfonyl fluoride.

AM-404

Also known as N-arachidonoylaminophenol.

AM-411

Produces similar effects to other cannabinoid agonists such as pain relief, sedation, and combatting anxiety.

AM-630

Aka (6-Iodopravadoline), it is a drug that acts as a potent and selective inverse agonist for the cannabinoid receptor CB2.

AM-661

1-(N-methyl-2-piperidine)methyl-2-methyl-3-(2-iodo)benzoylindole

AM-678

Aka JWH-018 (1-pentyl-3-(1-naphthoyl)indole), it is acts as a full agonist at both the CB1 and CB2 cannabinoid receptors and has been used in synthetic marijuana.

AM-679

A drug that acts as a moderately potent agonist for the cannabinoid receptors.

AM-694

Aka (1-(5-fluoropentyl)-3-(2-iodobenzoyl)indole) is a drug that acts as a potent and selective agonist for the cannabinoid receptor CB1.

AM-855

An analgesic drug which is a cannabinoid agonist.

AM-881

A chlorine-substituted stereoisomer of anandamide.

AM-883

A synthetic cannabinoid receptor agonist from the eicosanoid family.

AM-905

An analgesic drug which is a cannabinoid agonist.

AM-906

An analgesic drug which is a cannabinoid agonist.

AM-919

An analgesic drug which is a cannabinoid receptor agonist. It is a derivative of HU-210.

AM-926

A potent agonist at both the CB1 and CB2 cannabinoid receptors. It is a derivative of HU-210

AM-938

An analgesic drug which is a cannabinoid receptor agonist. It is a derivative of HU-210.

AM-1116

A dimethylated stereoisomer of anandamide.

AM-1172

An endocannabinoid analog specifically designed to be a potent and selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis.

AM-1220

A drug that acts as a potent and moderately selective agonist for the cannabinoid receptor CB1. Has been detected in synthetic marijuana.

AM-1221

A drug that acts as a potent and selective agonist for the cannabinoid receptor CB2.

AM-1235

Aka (1-(5-fluoropentyl)-3-(naphthalen-1-oyl)-6-nitroindole) is a drug that acts as a potent and reasonably selective agonist for the cannabinoid receptor CB1.

AM-1241

Aka(1-(methylpiperidin-2-ylmethyl)-3-(2-iodo-5-nitrobenzoyl)indole), it is a chemical from the aminoalkylindole family that acts as a potent and selective agonist for the cannabinoid receptor CB2

AM-1248

A drug that acts as a moderately potent agonist for both the cannabinoid receptors CB1 and CB2. The related compound 1-pentyl-3-(1-adamantoyl)indole has been sold as synthetic marijuana.

AM-1346

A synthetic cannabinoid receptor agonist from the eicosanoid family.

AM-1710

A CB2 selective cannabilactone.

AM-2201

AM-2201 (1-(5-fluoropentyl)-3-(1-naphthoyl)indole) is a research chemical that acts as a potent but nonselective full agonist for the cannabinoid receptor. Has reportedly been used as a recreational drug.

AM-2212

A potent agonist at both CB1 and CB2 cannabinoid receptors with dodecal selectivity for CB1.

AM-2213

A potent agonist at both CB1 and CB2 with 10x selectivity for CB1.

AM-2232

Aka (1-(4-cyanobutyl)-3-(naphthalen-1-oyl)indole) is a drug that acts as a potent but unselective agonist for the cannabinoid receptors.

AM-2233

A drug that acts as a highly potent full agonist for the cannabinoid receptors.

AM-2389

A classical cannabinoid derivative which acts as a potent and reasonably selective agonist for the CB1 receptor.

AM-3102

An analog of oleoylethanolamide, it also acts as a weak cannabinoid agonist.

AM-4030

A potent agonist at both the CB1 and CB2 cannabinoid receptors, it is dodecally selective for CB1. It is a derivative of HU-210.

AM-4054

A potent but slow-onset cannabinoid receptor agonist with CB1 cannabinoid receptor affinity.

AM-4113

A CB1 cannabinoid receptor selective neutral antagonist.

AM-6545

A drug which acts as a peripherally selective silent antagonist for the CB1 cannabinoid receptor, and was developed for the treatment of obesity.

AMG-1

An analgesic drug which is a cannabinoid agonist. It is a potent agonist at both the CB1 and CB2 receptors with moderate selectivity for the CB1 receptor.

AMG-3

An analgesic drug which is a cannabinoid agonist. It is a potent agonist at both the CB1 and CB2 receptors.

AMG-36

An analgesic drug which is a cannabinoid agonist. It is a potent agonist at both the CB1 and CB2 receptors with moderate selectivity for CB1.

AMG-41

An analgesic drug which is a cannabinoid agonist. It is a potent agonist at both the CB1 and CB2.

APICA

Aka SDB-001 or 2NE1, it is a drug that acts as a potent agonist for the cannabinoid receptors and has been identified as an ingredient in synthetic cannabis smoking blends.

α-Pyrrolidinopentiophenone

Aka alpha-Pyrrolidinovalerophenone,α-PVP, O-2387 or alpha-PVP, it is a stimulant compound developed in the 1960s and related to pyrovalerone and is believed to act similarly to the designer drug MDPV, which acts as a norepinephrine-dopamine reuptake inhibitor.

α-Pyrrolidinopropiophenone

Aka α-PPP, it is a stimulant drug that has been detected by laboratories in Germany as an ingredient in "ecstasy" tablets seized by law enforcement authorities.

Arachidonyl-2'-chloroethylamide

A synthetic agonist of the CB1 receptor with low affinity for the CB2 receptor.

Arachidonylcyclopropylamide

A synthetic agonist of the CB1 receptor with low affinity for the CB2 receptor.

AZ-11713908

A peripherally selective cannabinoid agonist, acting as a potent agonist at the CB1 receptor and a partial agonist at CB2

BAY 38-7271

Aka KN 38-7271, it is a drug which is a cannabinoid receptor agonist used in scientific research, with proposed uses in the treatment of traumatic brain injury and has fairly high affinity for both CB1 and CB2 receptors

BAY 59-3074

A drug which is a cannabinoid receptor partial agonist used in scientific research. It has modest affinity for both CB1 and CB2 receptors.

Canbisol

Aka Nabidrox, it is a synthetic cannabinoid derivative that is a potent agonist at both the CB1 and CB2 receptors. It is mainly used in scientific research but has been made illegal in some countries.

Cannabipiperidiethanone

A synthetic cannabinoid from the phenylacetylindole family that has been found as an ingredient of synthetic marijuana blends.

CB-13

Aka SAB-378, it is a cannabinoid drug that acts as a potent agonist at both the CB1 and CB2 receptors.

CB-86

A resorcinol-anandamide hybrid compound that acts as a partial agonist for the CB1 receptor and a neutral antagonist for the CB2 receptor.

CBS-0550

A drug that acts as a potent and selective cannabinoid CB2 receptor agonist.

CP 47,497

Aka Cannabicyclohexanol, it is a cannabinoid receptor agonist drug. It has been used in synthetic marijuana and is illegal in a handful of countries.

CP 50,556-1

Aka Levonantradol, it is a synthetic cannabinoid analog of dronabinol. It is around 30x more potent than THC.

CP 55,244

A compound which is a cannabinoid receptor agonist. It has pain relieving effects and is used in scientific research. It is an extremely potent CB1 cannabinoid receptor full agonist.

CP 55,940

A cannabinoid which mimics the effects of naturally occurring THC.

CP-945,598

Aka otenabant, it is a drug which acts as a potent and highly selective CB1 antagonist.

Desmethylprodine

Aka MPPP, it is an opioid analgesic drug developed in the 1940s that has been illegally manufactured for recreational drug use. It is an analog of Pethidine (Meperidine).

Dimethylheptylpyran

A synthetic analogue of THC.

Dronabinol

A pharmaceutical formulation of THC, it is available by prescription in the U.S. and Canada under the brand name Marinol.

EAM-2201

A Naphthoylindole type synthetic cannabinoid that is a hybrid of two known synthetic cannabinoid compounds: JWH-210 and AM-2201. It has been found as an ingredient in synthetic marijuana smoking products and has been banned in some countries.

GW-405,833

Aka L-768,242, it is a drug that acts as a potent and selective partial agonist for the CB2 cannabinoid receptor.

GW-842,166X

A drug which acts as a potent and selective cannabinoid CB2 receptor agonist, with a novel chemical structure based on a pyrimidine core.

HU-210

A synthetic cannabinoid that is 100 to 800 times more potent than natural THC. It has been implicated in preventing the inflammation caused by amyloid beta proteins involved in Alzheimer's disease, in addition to preventing cognitive impairment and loss of neuronal markers. It has been found in synthetic marijuana and is illegal in some countries.

HU-211

Aka Dexanabinol or ETS210, it is a synthetic cannabinoid derivative. Unlike other cannabinoid derivatives, HU-211 does not act as a cannabinoid receptor agonist.

HU-239

Aka ajulemic acid, AB-III-56 & IP-751, it is a synthetic cannabinoid derivative of the non-psychoactive THC metabolite 11-nor-9-carboxy-THC that shows useful analgesic and anti-inflammatory effects without causing a subjective "high".

HU-243

Aka AM-4056, it is a synthetic cannabinoid drug that is a potent agonist at both the CB1 and CB2 receptors.

HU-308

A drug that acts as a cannabinoid agonist. It is highly selective for the CB2 receptor.

HU-320

A drug related to cannabidiol, which has strong anti-inflammatory and immunosuppressive properties while demonstrating no psychoactive effects.

HU-331

An anticarcinogenic drug synthesized from cannabidiol.

HU-336

A strongly antiangiogenic compound.

HU-345

A strongly antiangiogenic compound.

HU-910

A nonclassical synthetic cannabinoid.

JTE 7-31

A selective cannabinoid receptor agonist.

JWH-007

An analgesic chemical from the naphthoylindole family, which acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It is illegal in some countries.

JWH-015

A chemical from the naphthoylindole family that acts as a subtype-selective cannabinoid agonist that has affinity for the CB2 receptor.

JWH-019

An analgesic chemical from the naphthoylindole family that acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It is illegal in some countries.

JWH-030

A research chemical which is a cannabinoid receptor agonist from the naphthoylpyrrole family that is used in scientific research. It is roughly half the potency of THC.

JWH-051

An analgesic drug which is a cannabinoid agonist. It retains high affinity for the CB1 receptor, but is a much stronger agonist for CB2.

JWH-057

A selective cannabinoid ligand.

JWH-073

An analgesic chemical from the naphthoylindole family that acts as a partial agonist at both the CB1 and CB2 cannabinoid receptors. It has been found in synthetic marijuana and is illegal in some countries.

JWH-081

An analgesic chemical from the naphthoylindole family, which acts as a cannabinoid agonist at both the CB1 and CB2 cannabinoid receptors.

JWH-098

A synthetic cannabinoid receptor agonist from the naphthoylindole family. It is illegal in some countries.

JWH-116

A synthetic cannabinoid receptor ligand from the naphthoylindole family.

JWH-120

A synthetic cannabimimetic from the naphthoylindole family.

JWH-122

A synthetic cannabimimetic from the naphthoylindole family.

JWH-133

A potent selective CB2 receptor agonist. It is implicated in preventing the inflammation caused by Amyloid beta proteins involved in Alzheimer's Disease, in addition to preventing cognitive impairment and loss of neuronal markers.

JWH-139

Chemical name; 3-(1,1-dimethylpropyl)-6,6,9-trimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromene

JWH-147

An analgesic drug used in scientific research, which acts as a cannabinoid agonist from the naphthoylpyrrole family at both the CB1 and CB2 receptors. It has been found in synthetic marijuana and has been banned in some countries.

JWH-148

A synthetic cannabimimetic.

JWH-149

A synthetic cannabimimetic from the naphthoylindole family.

JWH-161

A cannabinoid derivative that was designed as a hybrid between the dibenzopyran "classical" cannabinoid drugs and the novel indole derivatives.

JWH-164

A synthetic cannabinoid receptor agonist from the naphthoylindole family.

JWH-166

A potent and highly selective CB2 cannabinoid receptor agonist.

JWH-167

A synthetic cannabinoid from the phenylacetylindole family.

JWH-171

An analgesic drug which acts as a cannabinoid receptor agonist.

JWH-175

A drug from the naphthylmethylindole family which acts as a cannabinoid receptor agonist. It is illegal in some countries.

JWH-176

An analgesic drug which acts as a cannabinoid receptor agonist.

JWH-181

A potent cannabinoid agonist.

JWH-182

A potent cannabinoid agonist from the naphthoylindole family.

JWH-184

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-185

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-192

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-193

A drug from the aminoalkylindole family which acts as a cannabinoid receptor agonist.

JWH-194

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-195

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-196

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-197

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-198

A drug from the aminoalkylindole family which acts as a cannabinoid receptor agonist.

JWH-199

A synthetic cannabinoid receptor ligand from the naphthylmethylindole family.

JWH-200

Aka WIN 55,225, it’s an analgesic chemical from the aminoalkylindole family that acts as a cannabinoid receptor agonist.

JWH-203

A synthetic cannabinoid from the phenylacetylindole family.

JWH-205

Chemical name; 1-(2-methyl-1-pentylindol-3-yl)-2-phenylethanone

JWH-210

An analgesic chemical from the naphthoylindole family, which acts as a potent cannabinoid agonist at both the CB1 and CB2. It has been found in synthetic marijuana and is banned in some countries.

JWH-213

A potent and fairly selective CB2 agonist.

JWH-220

A cannabinoid agonist.

JWH-229

A potent CB2 agonist.

JWH-234

A cannabinoid agonist with CB2 selectivity.

JWH-249

A synthetic cannabinoid from the phenylacetylindole family.

JWH-250

A synthetic cannabinoid from the phenylacetylindole family. It has been found in synthetic marijuana.

JWH-251

A synthetic cannabinoid from the phenylacetylindole family.

JWH-253

A cannabinoid agonist.

JWH-258

A potent and mildly selective CB1 agonist.

JWH-300

A cannabinoid agonist.

JWH-302

A synthetic cannabinoid from the phenylacetylindole family.

JWH-307

An analgesic drug used in scientific research, which acts as a cannabinoid agonist from the naphthoylpyrrole family at both the CB1 and CB2 receptors. It has been found in synthetic marijuana.

JWH-336

A cannabinoid agonist.

JWH-350

A cannabinoid agonist with an affinity for the CB2 cannabinoid receptor.

JWH-359

A potent and selective CB2 receptor agonist.

JWH-369

A synthetic cannabinoid receptor agonist from the naphthoylpyrrole family.

JWH-370

A synthetic cannabinoid receptor agonist from the naphthoylpyrrole family.

JWH-387

Chemical name; 1-pentyl-3-(4-bromo-1-naphthoyl)indole, it’s an analgesic chemical from the naphthoylindole family, which acts as a potent cannabinoid agonist at both receptors.

JWH-398

An analgesic chemical from the naphthoylindole family, which acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It has been found in synthetic marijuana.

JWH-424

A drug from the naphthoylindole family, which acts as a cannabinoid agonist at both the CB1 and CB2 receptors, but with moderate selectivity for CB2.

KM-233

A drug which is an analogue of THC. It has high binding affinity for both the CB1 and CB2 receptors, with a selectivity for CB2.

LASSBio-881

A drug which acts as both a non-selective partial agonist of the CB1 and CB2 cannabinoid receptors, and also as an antagonist of the TRPV1 receptor.

LBP-1

A drug that acts as a potent and selective cannabinoid receptor agonist, with high potency at both the CB1 and CB2 receptors.

Leelamine

A weak CB1 receptor agonist and PDK inhibitor.

L-759,633

An analgesic drug that is a cannabinoid agonist. It is a fairly selective agonist for the CB2 receptor, with selectivity for CB2.

L-759,656

An analgesic drug that is a cannabinoid agonist. It is a highly selective agonist for the CB2 receptor.

MAM-2201

A Naphthoylindole type synthetic cannabinoid that is a hybrid of two known synthetic cannabinoid compounds: JWH-122 and AM-2201. It has been found as an ingredient in synthetic marijuana smoking products and has been banned in some countries.

MDA-7

A synthetic cannabinoid agonist.

MDA-19

A drug that acts as a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor.

MDPPP

Aka 3',4'-Methylenedioxy-α-pyrrolidinopropiophenone, it is a stimulant designer drug. It was sold in Germany in the late 1990s and early 2000s as an ingredient in imitation ecstasy (MDMA) pills

Menabitan

Aka SP-204, or menabitan hydrochloride, it is a synthetic drug which acts as a potent cannabinoid receptor agonist. It is closely related to natural cannabinoids

Mephedrone

A synthetic stimulant drug of the amphetamine and cathinone classes, it is chemically similar to the cathinone compounds found in the khat plant of eastern Africa. It comes in the form of tablets or a powder, which users can swallow, snort or inject, producing similar effects to MDMA, amphetamines and cocaine. It has been found as an ingredient in “bath salts” drugs.

Methylenedioxypyrovalerone

A psychoactive drug with stimulant properties, which acts as a norepinephrine-dopamine reuptake inhibitor (NDRI). First developed in 1969, it has been found to be an ingredient in “bath salts” drugs.

Methylone

Aka M1, it is an entactogen and stimulant of the phenethylamine, amphetamine and cathinone classes. It has been found to be an ingredient in designer drugs similar to “bath salts” drugs and is illegal in some countries.

Nabazenil

Aka SP-175, it is a synthetic cannabinoid receptor agonist, which has anticonvulsant properties.

Nabilone

A synthetic cannabinoid with therapeutic use as an antiemetic and as an adjunct analgesic for neuropathic pain. In Canada, the United States, the United Kingdom and Mexico, nabilone is marketed as Cesamet.

Nabitan

Aka Nabutam, Benzopyranoperidine, SP-106 or Abbott 40656, it is a synthetic cannabinoid analog of dronabinol (Marinol).

Naboctate

Aka SP-325, it is a synthetic cannabinoid receptor agonist.

Naphyrone

Aka O-2482 and naphthylpyrovalerone. it is a drug derived from pyrovalerone that acts as a triple reuptake inhibitor, producing stimulant effects and has been reported as a novel designer drug.

NMP-7

A drug which acts as both a non-selective agonist of the CB1 and CB2 cannabinoid receptors, and also as a blocker of T-type calcium channels.

Nonabine

Aka BRL-4664, it is a cannabinoid derivative, which was developed for the prevention of nausea and vomiting associated with cancer chemotherapy.

O-224

A classical synthetic cannabinoid.

O-581

A classical synthetic cannabinoid.

O-585

A synthetic cannabinoid receptor agonist from the eicosanoid family.

O-689

A synthetic cannabinoid receptor agonist from the eicosanoid family.

O-774

A classical cannabinoid derivative which acts as a potent agonist for the cannabinoid receptors,

O-806

A drug which is a cannabinoid derivative that is used in scientific research. It is described as a mixed agonist/antagonist at the cannabinoid receptor CB1, meaning that it acts as an antagonist when co-administered alongside a more potent CB1 agonist, but exhibits weak partial agonist effects when administered by itself.

O-823

A drug which is a cannabinoid derivative that is used in scientific research described as a mixed agonist/antagonist at the cannabinoid receptor CB1, meaning that it acts as an antagonist when co-administered alongside a more potent CB1 agonist, but exhibits weak partial agonist effects when administered by itself.

O-889

A synthetic cannabinoid receptor agonist.

O-1057

An analgesic cannabinoid derivative created for use in scientific research. It is water soluble and has moderate affinity for both CB1 and CB2 receptors.

O-1125

A drug which is a cannabinoid derivative. It has analgesic effects and is used in scientific research. It is a potent CB1 full agonist.

O-1191

A classical synthetic cannabinoid.

O-1238

A drug which is a cannabinoid derivative that is used in scientific research. It is a partial agonist at the cannabinoid receptor CB1.

O-1269

A drug that is a diarylpyrazole derivative and a cannabinoid receptor agonist.

O-1270

A synthetic cannabinoid receptor agonist.

O-1376

A nonclassical synthetic cannabinoid.

O-1399

A synthetic cannabinoid receptor agonist.

O-1422

A nonclassical synthetic cannabinoid.

O-1601

A nonclassical synthetic cannabinoid.

O-1602

A synthetic compound most closely related to abnormal cannabidiol, and more distantly related in structure to cannabinoid drugs such as THC. It does not bind to the classical cannabinoid receptors CB1 or CB2 with any significant affinity, but instead is an agonist at several other receptors which appear to be related to the cannabinoid receptors, particularly GPR18 and GPR55.

O-1656

A nonclassical synthetic cannabinoid.

O-1657

A nonclassical synthetic cannabinoid.

O-1811

A synthetic cannabinoid receptor agonist.

O-1812

An eicosanoid derivative related to anandamide that acts as a potent and highly selective agonist for the CB1 receptor.

O-1839

A synthetic cannabinoid receptor agonist.

O-1856

A synthetic cannabinoid receptor agonist.

O-1860

A synthetic cannabinoid receptor agonist from the eicosanoid family.

O-1861

A "hybrid" agonist of the CB1 and VR1 vanilloid receptors and a compound with potential therapeutic importance. It is from the eicosanoid family.

O-1895

A synthetic cannabinoid receptor agonist.

O-1918

A synthetic compound related to cannabidiol, which is an antagonist at two former orphan receptors GPR18 and GPR55, that appear to be related to the cannabinoid receptors.

O-2048

A classical synthetic cannabinoid.

O-2050

A drug that is a classical cannabinoid derivative, which acts as a silent antagonist for the CB1 receptor.

O-2113

A drug that is a classical cannabinoid derivative, which acts as a potent agonist for cannabinoid receptors.

O-2220

A synthetic cannabinoid receptor agonist.

O-2365

A classical synthetic cannabinoid.

O-2372

An analgesic cannabinoid derivative created for use in scientific research. It has high affinity for both CB1 and CB2 receptors. It is moderately water soluble.

O-2373

A classical synthetic cannabinoid.

O-2383

A classical synthetic cannabinoid.

O-2426

A classical synthetic cannabinoid.

O-2484

A classical synthetic cannabinoid.

O-2545

An analgesic cannabinoid derivative created for use in scientific research. It is water soluble and has high affinity for both CB1 and CB2 receptors.

O-2694

A drug that is a cannabinoid derivative. It has analgesic effects and is used in scientific research. It is highly water-soluble and has high affinity for both CB1 and CB2 receptors.

O-2715

A classical synthetic cannabinoid.

O-2716

A classical synthetic cannabinoid.

O-3223

A classical synthetic cannabinoid.

O-3226

A classical synthetic cannabinoid.

Org 28312

A drug which acts as a potent cannabinoid receptor full agonist at both the CB1 and CB2 receptors.

Org 28611

Aka SCH-900,111, it is a drug which acts as a potent cannabinoid receptor full agonist at both the CB1 and CB2 receptors.

Parahexyl

A synthetic homologue of THC. It is illegal in some countries.

Pentedrone

Aka 2-(methylamino)-1-phenylpentan-1-one or α-methylamino-valerophenone, it is a designer drug with presumably stimulant effects, which has been found since 2010 as an ingredient in a number of "bath salt" mixes sold as legal highs.

PF-03550096

A drug that acts as a potent agonist for the CB2 cannabinoid receptor.

Pirnabine

Aka SP-304, it is a synthetic cannabinoid receptor ligand, which was developed for the treatment of glaucoma.

Pravadoline

Aka WIN 48,098, it is an antiinflammatory and analgesic developed in the 1980s as a new antiinflammatory and prostaglandin synthesis inhibitor. It was eventually discovered that pravadoline represented the first compound from a novel class of cannabinoid agonists, the aminoalkylindoles.

QUCHIC

Aka BB-22, it is a designer drug offered by online vendors as a cannabimimetic agent and has been detected as an ingredient in synthetic marijuana products.

QUPIC

Aka PB-22, it is a designer drug offered by online vendors as a cannabimimetic agent and has been detected as an ingredient in synthetic marijuana products.

RCS-4

RCS-4, or 1-pentyl-3-(4-methoxybenzoyl)indole, is a synthetic cannabinoid drug sold under the names SR-19, BTM-4, or Eric-4 (later shortened to E-4), but originally, OBT-199. It has been found in synthetic marijuana and is illegal in some countries.

RCS-8

Aka SR-18, BTM-8 or 1-(2-cyclohexylethyl)-3-(2-methoxyphenylacetyl), it is a synthetic cannabinoid from the phenylacetylindole family that has been found as an ingredient of synthetic marijuana blends.

S-444,823

A cannabinoid agonist that has moderate selectivity for the CB2 cannabinoid receptor.

SER-601

Aka COR-167, it is a drug that acts as a potent and selective cannabinoid CB2 receptor agonist.

SPA-239

A synthetic nonclassical cannabinoid.

STS-135

A designer drug offered by online vendors as a cannabimimetic agent.

Tedalinab

Aka GRC-10693, it is a drug which acts as a potent and selective cannabinoid CB2 receptor agonist.

THC-O-acetate

Aka THC acetate ester, it is a derivative of THC apparently made by extracting and purifying THC from cannabis plant material using a soxhlet extractor, followed by reaction with acetic anhydride similar to how heroin is made from morphine.

THC-O-phosphate

A water-soluble phosphate ester derivative of THC invented in 1978 and made by reacting THC with phosphoryl chloride using pyridine as a solvent, followed by quenching with water to produce THC phosphate ester.

Tinabinol

Aka SP-119 it is a synthetic cannabinoid drug and analogue of dronabinol.

UR-12

Aka MN-25, it is a drug that acts as a reasonably selective agonist of peripheral cannabinoid receptors. It has moderate affinity for CB2 receptors with a lower affinity for the psychoactive CB1 receptors.

UR-144

Aka TMCP-018, KM-X1, MN-001 or YX-17, it isa drug that acts as a selective full agonist of the peripheral cannabinoid receptor CB2. It has been found in synthetic marijuana and has been banned in some countries.

URB-447

A synthetic cannabinoid receptor agonist.

URB-754

A synthetic designer drug that has been found in synthetic marijuana products that acts by inhibiting an endocannabinoid deactivating enzyme.

VSN-16

A novel water-soluble cannabinoid agonist.

WIN 54,461

Aka 6-Bromopravadoline, it is a drug that acts as a potent and selective inverse agonist for the cannabinoid receptor CB2.

WIN 55,212-2

A chemical described as an aminoalkylindole derivative, which produces effects similar to those of cannabinoids like THC.

WIN 55,225

Aka JWH-200, it’s an analgesic chemical from the aminoalkylindole family that acts as a cannabinoid receptor agonist.

WIN 56,098

A chemical that is considered to be an aminoalkylindole derivative. It is a tricyclic aryl derivative that acts as a competitive antagonist at the CB2 cannabinoid receptor.

XLR-11

A synthetic designer drug that has been found in synthetic marijuana products. It has been banned in some countries


 
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