| dbo:abstract |
6-APB (6-(2-aminopropyl)benzofuran) is an empathogenic psychoactive compound of the substituted benzofuran and substituted phenethylamine classes. 6-APB and other compounds are sometimes informally called "Benzofury" in newspaper reports. It is similar in structure to MDA, but differs in that the 3,4-methylenedioxyphenyl ring system has been replaced with a benzofuran ring. 6-APB is also the unsaturated benzofuran derivative of 6-APDB. It may appear as a tan grainy powder. While the drug never became particularly popular, it briefly entered the rave and underground clubbing scene in the UK before its sale and import were banned. It falls under the category of research chemicals, sometimes called "legal highs." Because 6-APB and other substituted benzofurans have not been explicitly outlawed in some countries, they are often technically legal, contributing to their popularity. (en) Le 6-(2-aminopropyl)benzofurane ou 1-benzofuran-6-ylpropan-2-amine est un composé entactogène de la classe des phényléthylamines. Sa structure est similaire au MDA mais diffère par la présence d'un cycle benzofurane à la place du cycle . Cet agent fait partie des nouveaux produits de synthèse. Le 6-APB est également le dérivé insaturé du 6-APDB. (fr) La 6-APB (nome chimico 6-(2-amminopropil)benzofurano ma conosciuto colloquialmente anche col nome di benzofury) è una sostanza psicoattiva dagli effetti psicostimolanti ed e empatogeni sviluppata nel 1993 dal farmacologo americano David Nichols come analogo non neurotossico dell'MDMA (ecstasy) da utilizzare come adiuvante della terapia psicologica (attualmente l'MDMA è in sperimentazione nel trattamento di alcuni disturbi psichiatrici). Ad oggi non è stata ancora sperimentata in ambito clinico ma negli ultimi anni è divenuta popolare come stupefacente per i suoi effetti molto simili a quelli dell'ecstasy e per essere tecnicamente una sostanza non controllata e quindi legale in molti stati. In Italia è stata prontamente inserita nella tabella 1 delle sostanze controllate. (it) 6-(2-aminopropyl)benzofuran of 1-benzofuran-6-ylpropan-2-amine (6-APB, ook bekend als Benzo Fury en Benfamine) is een stimulerende empathogene designer drug die wordt gebruikt als partydrug. De stof is chemisch verwant aan amfetamine. De drug lijkt op mdma, alleen zou het effect van 6-APB langer duren. Benzo Fury is ontwikkeld in Engeland en wordt sinds 2010 via internet verkocht met de mededeling dat deze niet geschikt is voor menselijke consumptie. Benzo Fury is nog niet opgenomen in drugswetten. (nl) 6-(2-Aminopropylo)benzofuran, 6-APB – organiczny związek chemiczny, entaktogen, pochodna amfetaminy. Jest również analogiem 3,4-metylenodioksyamfetaminy (MDA) i . (pl) |
| dbo:casNumber |
286834-84-2 (HCl) 286834-85-3 |
| dbo:fdaUniiCode |
285VE60914 |
| dbo:pubchem |
9794343 |
| dbo:thumbnail |
wiki-commons:Special:FilePath/Benzofuran2DACSL.svg?width=300 |
| dbo:wikiPageExternalLink |
https://www.protestkit.eu/results/ |
| dbo:wikiPageID |
27704959 (xsd:integer) |
| dbo:wikiPageLength |
18918 (xsd:nonNegativeInteger) |
| dbo:wikiPageRevisionID |
1116845242 (xsd:integer) |
| dbo:wikiPageWikiLink |
dbr:Canadian_Institutes_of_Health_Research dbr:Potency_(pharmacology) dbr:Properties_of_water dbr:Psychoactive_drug dbr:Psychosis dbr:Benzofuran dbr:Anorectic dbr:Hydrogen_chloride dbr:Betäubungsmittelgesetz dbr:United_States dbr:Dopamine_transporter dbr:Structural_analog dbr:Liebermann_reagent dbr:1,3-benzodioxole dbc:Designer_drugs dbc:Entactogens_and_empathogens dbc:Serotonin-norepinephrine-dopamine_releasing_agents dbc:Serotonin_receptor_agonists dbr:Structural_isomer dbr:Monoamine_neurotransmitter dbr:Full_agonist dbr:Furan dbr:Germany dbr:Controlled_Drugs_and_Substances_Act dbr:Opium_Law dbr:Luxembourg dbr:Silica_gel dbr:Column_chromatography dbr:Froehde_reagent dbr:Functional_group dbr:Australia dbr:BW-723C86 dbc:6-Benzofuranethanamines dbr:UK dbr:Drug_metabolism dbr:Drugs_controlled_by_the_German_Betäubungsmittelgesetz dbr:Drugs_controlled_by_the_UK_Misuse_of_Drugs_Act dbr:Safe_Streets_Act dbr:3,4-Methylenedioxyamphetamine dbr:5-APB dbr:6-APDB dbr:Acetal dbr:Alcohol_(chemistry) dbr:Amphetamine dbr:5-HT2A_receptor dbr:5-HT2B_receptor dbr:5-HT2C_receptor dbr:Fenfluramine dbr:Folin's_reagent dbr:France dbr:Carboxylic_acid dbr:Benzofury_(disambiguation) dbr:Glucuronidation dbr:Research_chemical dbc:5-HT2B_agonists dbc:Substituted_amphetamines dbr:Italy dbr:Hydrochloride dbr:Hydroxylation dbr:Federal_Analog_Act dbr:Simon's_reagent dbr:Chloroform dbr:Aldehyde dbr:Affinity_(pharmacology) dbr:Binding_selectivity dbr:Biological_target dbr:Sweden dbr:Ehrlich's_reagent dbr:3,4-methylenedioxyamphetamine dbr:Sodium_hydride dbr:Controlled_Drug_in_United_Kingdom dbr:Empathogen-entactogen dbr:Netherlands dbr:New_Zealand dbr:Serotonergic dbr:Serotonin dbr:Serotonin-norepinephrine-dopamine_releasing_agent dbr:Serotonin–norepinephrine–dopamine_reuptake_inhibitor dbr:Marquis_reagent dbr:Mecke_reagent dbr:Serotonin_transporter dbr:Substituted_phenethylamine dbr:Pharmacokinetics dbr:Reuptake dbr:Substituted_benzofuran dbr:Mandelin_reagent dbr:Monoamine_transporter dbr:Norepinephrine_transporter dbr:Releasing_agent dbr:Ion_pair dbr:Temporary_class_drug dbr:Transporter_blocker dbr:Polyphosphoric_acid dbr:Chemical_reduction dbr:3-bromophenol dbr:Cardiotoxic dbr:Α2C-adrenergic_receptor dbr:Withdrawn_drug dbr:3-carboxymethyl-4-hydroxyamphetamine dbr:4-carboxymethyl-3-hydroxyamphetamine dbr:Bromoacetaldehyde dbr:File:Synthesis_of_6-APB_and_its_structural_isomer_4-APB.png |
| dbp:alt |
Ball-and-stick model of the 6-APB molecule (en) |
| dbp:atcPrefix |
none (en) |
| dbp:c |
11 (xsd:integer) |
| dbp:casNumber |
286834 (xsd:integer) |
| dbp:casSupplemental |
286834 (xsd:integer) |
| dbp:chemspiderid |
7970110 (xsd:integer) |
| dbp:h |
13 (xsd:integer) |
| dbp:image |
6 (xsd:integer) |
| dbp:iupacName |
1 (xsd:integer) |
| dbp:legalCa |
Schedule III (en) |
| dbp:legalDe |
Anlage II (en) |
| dbp:legalUk |
Class B (en) |
| dbp:n |
1 (xsd:integer) |
| dbp:o |
1 (xsd:integer) |
| dbp:pubchem |
9794343 (xsd:integer) |
| dbp:smiles |
NCCC1=CC=C2C=C1 (en) |
| dbp:stdinchi |
1 (xsd:integer) |
| dbp:stdinchikey |
FQDAMYLMQQKPRX-UHFFFAOYSA-N (en) |
| dbp:unii |
285 (xsd:integer) |
| dbp:verifiedfields |
changed (en) |
| dbp:verifiedrevid |
477225566 (xsd:integer) |
| dbp:watchedfields |
changed (en) |
| dbp:wikiPageUsesTemplate |
dbt:Citation_needed dbt:Drugbox dbt:Entactogens dbt:Hallucinogens dbt:Phenethylamines dbt:Reflist dbt:Short_description dbt:Unreliable_source? dbt:Not_in_citation dbt:Cascite dbt:Chemspidercite dbt:Fdacite dbt:Stdinchicite |
| dcterms:subject |
dbc:Designer_drugs dbc:Entactogens_and_empathogens dbc:Serotonin-norepinephrine-dopamine_releasing_agents dbc:Serotonin_receptor_agonists dbc:6-Benzofuranethanamines dbc:5-HT2B_agonists dbc:Substituted_amphetamines |
| gold:hypernym |
dbr:Compound |
| rdf:type |
owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q8386 yago:WikicatAmphetamines yago:WikicatSerotonin-norepinephrine-dopamineReuptakeInhibitors yago:Agent114778436 yago:Amphetamine102704153 yago:CausalAgent100007347 yago:DesignerDrug103179489 yago:Drug103247620 yago:DrugOfAbuse103248958 yago:Inhibitor114724436 yago:Matter100020827 yago:PhysicalEntity100001930 yago:PsychoactiveDrug104017137 dbo:ChemicalCompound dbo:Drug yago:Stimulant104320126 yago:Substance100020090 yago:WikicatDesignerDrugs |
| rdfs:comment |
Le 6-(2-aminopropyl)benzofurane ou 1-benzofuran-6-ylpropan-2-amine est un composé entactogène de la classe des phényléthylamines. Sa structure est similaire au MDA mais diffère par la présence d'un cycle benzofurane à la place du cycle . Cet agent fait partie des nouveaux produits de synthèse. Le 6-APB est également le dérivé insaturé du 6-APDB. (fr) 6-(2-aminopropyl)benzofuran of 1-benzofuran-6-ylpropan-2-amine (6-APB, ook bekend als Benzo Fury en Benfamine) is een stimulerende empathogene designer drug die wordt gebruikt als partydrug. De stof is chemisch verwant aan amfetamine. De drug lijkt op mdma, alleen zou het effect van 6-APB langer duren. Benzo Fury is ontwikkeld in Engeland en wordt sinds 2010 via internet verkocht met de mededeling dat deze niet geschikt is voor menselijke consumptie. Benzo Fury is nog niet opgenomen in drugswetten. (nl) 6-(2-Aminopropylo)benzofuran, 6-APB – organiczny związek chemiczny, entaktogen, pochodna amfetaminy. Jest również analogiem 3,4-metylenodioksyamfetaminy (MDA) i . (pl) 6-APB (6-(2-aminopropyl)benzofuran) is an empathogenic psychoactive compound of the substituted benzofuran and substituted phenethylamine classes. 6-APB and other compounds are sometimes informally called "Benzofury" in newspaper reports. It is similar in structure to MDA, but differs in that the 3,4-methylenedioxyphenyl ring system has been replaced with a benzofuran ring. 6-APB is also the unsaturated benzofuran derivative of 6-APDB. It may appear as a tan grainy powder. While the drug never became particularly popular, it briefly entered the rave and underground clubbing scene in the UK before its sale and import were banned. It falls under the category of research chemicals, sometimes called "legal highs." Because 6-APB and other substituted benzofurans have not been explicitly outlawe (en) La 6-APB (nome chimico 6-(2-amminopropil)benzofurano ma conosciuto colloquialmente anche col nome di benzofury) è una sostanza psicoattiva dagli effetti psicostimolanti ed e empatogeni sviluppata nel 1993 dal farmacologo americano David Nichols come analogo non neurotossico dell'MDMA (ecstasy) da utilizzare come adiuvante della terapia psicologica (attualmente l'MDMA è in sperimentazione nel trattamento di alcuni disturbi psichiatrici). (it) |
| rdfs:label |
6-APB (en) 6-APB (it) 6-(2-Aminopropyl)benzofurane (fr) 6-APB (nl) 6-(2-Aminopropylo)benzofuran (pl) |
| owl:sameAs |
freebase:6-APB yago-res:6-APB wikidata:6-APB dbpedia-fr:6-APB dbpedia-it:6-APB dbpedia-nl:6-APB dbpedia-pl:6-APB dbpedia-sh:6-APB dbpedia-sr:6-APB https://global.dbpedia.org/id/2WLi1 |
| prov:wasDerivedFrom |
wikipedia-en:6-APB?oldid=1116845242&ns=0 |
| foaf:depiction |
wiki-commons:Special:FilePath/6-APB_molecule_ball.png wiki-commons:Special:FilePath/Benzofuran2DACSL.svg wiki-commons:Special:FilePath/Synthesis_of_6-APB_and_its_structural_isomer_4-APB.png |
| foaf:isPrimaryTopicOf |
wikipedia-en:6-APB |
| is dbo:wikiPageDisambiguates of |
dbr:APB |
| is dbo:wikiPageRedirects of |
dbr:6-apb dbr:6-(2-Aminopropyl)benzofuran dbr:6-(2-aminopropyl)benzofuran dbr:Eric-7 dbr:NRG-7 |
| is dbo:wikiPageWikiLink of |
dbr:6-apb dbr:Psychoactive_drug dbr:List_of_designer_drugs dbr:David_E._Nichols dbr:Substituted_amphetamine dbr:Liebermann_reagent dbr:List_of_psychedelic_drugs dbr:TAAR1 dbr:Empathogen–entactogen dbr:Froehde_reagent dbr:2-MAPB dbr:BW-723C86 dbr:6-MAPDB dbr:Drugs_controlled_by_the_German_Betäubungsmittelgesetz dbr:6-APDB dbr:6-EAPB dbr:6-MAPB dbr:5-HT2B_receptor dbr:5-HT_receptor dbr:Benzofury dbr:APB dbr:C11H13NO dbr:Substituted_benzofuran dbr:Substituted_methylenedioxyphenethylamine dbr:Serotonin–norepinephrine–dopamine_releasing_agent dbr:6-(2-Aminopropyl)benzofuran dbr:6-(2-aminopropyl)benzofuran dbr:Temporary_class_drug dbr:Eric-7 dbr:NRG-7 |
| is foaf:primaryTopic of |
wikipedia-en:6-APB |
