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Chemical compound
MY400. Substituted benzothiophene 6-MAPBT BK-5-MAPBT 5-MAPDI BK-5-MAPB IBF5MAP MDMA Methamnetamine TDMA Mydecine (5 January 2024). "Novel short-acting
5-MAPBT
Pharmaceutical compound
BK-5-MAPBT, also known as β-keto-5-MAPBT, is a possible entactogen of the benzothiophene and cathinone families. It is a potent monoamine releasing agent
BK-5-MAPBT
Chemical compound
Substituted benzofuran Substituted cathinone βk-6-MAPB, 5-MAPB, and 6-MAPB TACT411 and TACT833 BK-5-MAPBT WO 2021/252538, Baggott M, "Advantageous benzofuran
BK-5-MAPB
Pharmaceutical compound
6-MAPBT, also known as 6-(2-(methylamino)propyl)-1-benzothiophene, is a possible entactogen of the phenethylamine, amphetamine, and benzothiophene families
6-MAPBT
Pharmaceutical compound
BK-5F-NM-AMT, or βk-5F-NM-αMT, also known as β-keto-5-fluoro-N-methyl-αMT or α,N-dimethyl-5-fluoro-β-ketotryptamine, is a monoamine releasing agent of
BK-5F-NM-AMT
Antidepressant medication
to the exceptionally high affinity of the drug for the histamine H1, 5-HT2A, and 5-HT2C receptors; exhibiting near exclusive occupation of these receptors
Mirtazapine
Class of psychoactive drugs that produce empathic experiences
entactogens, such as the benzofurans 5-MAPB, 6-MAPB, BK-5-MAPB, and BK-6-MAPB, have unexpectedly been found to be potent serotonin 5-HT1B receptor agonists. In
Entactogen
Psychedelic drug
5-MeO-NMT, 5-MeO-MET, 5-MeO-DET, 5-MeO-MPT, 5-MeO-EPT, 5-MeO-DPT, 5-MeO-MiPT, 5-MeO-EiPT, 5-MeO-PiPT, 5-MeO-DiPT, 5-MeO-MALT, 5-MeO-DALT, 5-MeO-pyr-T, 5-EtO-DMT
5-MeO-DMT
Monoamine releaser and entactogen
of BK-NM-AMT include α-methyltryptamine (AMT) and α,N-dimethyltryptamine (α,N-DMT; NM-AMT), among others. Several 5-halogenated derivatives of BK-NM-AMT
BK-NM-AMT
Mammalian protein found in Homo sapiens
5-HT2A agonist) 5-Carboxamidotryptamine (5-CT) 5-MAPB 5-MAPBT 6-MAPB 6-MAPBT Almotriptan Anpirtoline (D-16949) Avitriptan Batoprazine BK-5-MAPB BK-5-MAPBT
5-HT1B_receptor
American pharmaceutical company
include benzofurans like 5-MAPB, 6-MAPB, 5-MBPB, 6-MBPB, BK-5-MAPB, and BK-6-MAPB, benzothiophenes like 5-MAPBT, 6-MAPBT, and BK-5-MAPBT, α-alkyl- and β-ketotryptamines
Tactogen
Psychoactive drug, often called ecstasy
MDOH, MDMOH (FLEA), N-t-BOC-MDMA, methylone (MDMC), MBDB, 5-MAPB, 6-MAPB, 5-MAPBT, 6-MAPBT, SDMA, ODMA, SeDMA, TDMA, MDAI, and MDAT, among many others
MDMA
Pharmaceutical compound
βk-6-MAPB, or BK-6-MAPB, also known as NM-PrBF6 or as 6-[2-(methylamino)propanoyl]benzofuran, is a putative entactogen of the benzofuran and cathinone
BK-6-MAPB
Pharmaceutical compound
BK-5Br-NM-AMT, or βk-5Br-NM-αMT, also known as β-keto-5-bromo-N-methyl-αMT or α,N-dimethyl-5-bromo-β-ketotryptamine, is a monoamine releasing agent of
BK-5Br-NM-AMT
Pharmaceutical compound
concentration = 400 nM). 5-APBT was first described in the scientific literature by 2020. Substituted benzothiophene 5-MAPBT 6-APBT 5-APB 5-APDB 5-API 3-APBT Brandt
5-APBT
Medication to prevent nausea and vomiting
pregnancy but has not been well studied in this group. It is a serotonin 5-HT3 receptor antagonist. It does not have any effect on dopamine receptors
Ondansetron
Pharmaceutical compound
(MY400) 6-APBT 6-MAPBT (MY300) 7-APBT Cathinones: BK-5-MAPBT Benzothiazoles Amphetamines: 5-BZT-MDA 5-BZT-MDMA 6-BZT-MDA 6-BZT-MDMA Benzoxathioles Amphetamines:
MDM1EA
Drug class
Wetsel WC, Irwin JJ, Skiniotis G, Shoichet BK, Roth BL, Ellman JA (October 2022). "Bespoke library docking for 5-HT2A receptor agonists with antidepressant
Serotonin 5-HT2A receptor agonist
Serotonin_5-HT2A_receptor_agonist
Chemical compound
related drugs. Substituted benzofuran Borax combo 6-MAPB, 5-APB, and 6-APB BK-5-MAPB and BK-6-MAPB TACT411 and TACT833 Oeri HE (May 2021). "Beyond ecstasy:
5-MAPB
Psychedelic drug
BK, Huidobro-Toro JP (June 2002). "Differences in potency and efficacy of a series of phenylisopropylamine/phenylethylamine pairs at 5-HT(2A) and 5-HT(2C)
2C-B
Species of psychoactive cactus
1007/978-3-642-70128-3_4. ISBN 978-3-642-70130-6. Retrieved 20 May 2025. Cassels BK, Sáez-Briones P (October 2018). "Dark Classics in Chemical Neuroscience: Mescaline"
Peyote
Naturally occurring psychedelic compound
BK, et al. (June 2007). "Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A
Mescaline
Chemical compound
5-Hydroxytryptophan (5-HTP), used medically as oxitriptan, is a naturally occurring amino acid and chemical precursor as well as a metabolic intermediate
5-Hydroxytryptophan
SSRI antidepressant
263–267. doi:10.1016/0002-9378(76)90154-x. PMID 2013. Koda-Kimble MA, Alldredge BK (2012). Applied therapeutics: the clinical use of drugs (10th ed.). Baltimore:
Fluoxetine
Psychedelic drug found in toads, mushrooms and plants
Bufotenin, also known as dimethylserotonin or as 5-hydroxy-N,N-dimethyltryptamine (5-HO-DMT), is a serotonergic psychedelic of the tryptamine family.
Bufotenin
Subtype of serotonin receptor
BK, et al. (June 2007). "Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A
5-HT2A_receptor
Chemical compound
5-Hydroxyindole (5-indolol or NSC 87503) is an indole alkaloid mood enhancer. It is a positive allosteric modulator of the serotonin 5-HT3 receptor. "5-Hydroxyindole
5-Hydroxyindole
Serotonergic psychoplastogen
5-MeO-isoDMT, or 5-OMe-isoDMT, also known as 5-methoxy-N,N-dimethylisotryptamine, is a prospective non-hallucinogenic serotonin 5-HT2A receptor agonist
5-MeO-isoDMT
Chemical compound
PMC 4211607. PMID 25193229. Reyes-Parada M, Iturriaga-Vasquez P, Cassels BK (2019). "Amphetamine Derivatives as Monoamine Oxidase Inhibitors". Front Pharmacol
5-Fluoro-AET
Medication
8 nM), where it is a receptor antagonist, and is also a mixed 5-HT3 receptor antagonist/5-HT4 receptor agonist. The antiemetic action of metoclopramide
Metoclopramide
Chemical compound
BIMU-8 is a drug which acts as a 5-HT4 receptor selective agonist. BIMU-8 was one of the first compounds of this class. The main action of BIMU-8 is to
BIMU8
Pharmaceutical compound
also known as 1-(5-methoxybenzofuran-3-yl)-2-aminopropane or 5-methoxy-3-(2-aminopropyl)benzofuran (5-MeO-3-APB) as well as 1-oxa-5-MeO-AMT, is a serotonin
Mebfap
Entactogen, stimulant, and psychedelic drug of the amphetamine family
agent (SNDRA) and a serotonin 5-HT2 receptor agonist, including of the serotonin 5-HT2A receptor. It has a duration of 5 to 8 hours or around 6 hours typically
3,4-Methylenedioxyamphetamine
Chemical compound
PMID 25547199. Toro-Sazo M, Brea J, Loza MI, Cimadevila M, Cassels BK (2019). "5-HT2 receptor binding, functional activity and selectivity in N-benzyltryptamines"
5-MeO-T-NBOMe
Tricyclic antidepressant
1986). "Pharmacological differentiation and characterization of 5-HT1A, 5-HT1B, and 5-HT1C binding sites in rat frontal cortex". Journal of Neurochemistry
Amitriptyline
Type of medication
placebo-controlled trial". Archives of General Psychiatry. 56 (5): 431–7. doi:10.1001/archpsyc.56.5.431. PMC 1475805. PMID 10232298. Liebowitz MR, Quitkin FM
Monoamine_oxidase_inhibitor
Pharmaceutical compound
(MY400) 6-APBT 6-MAPBT (MY300) 7-APBT Cathinones: BK-5-MAPBT Benzothiazoles Amphetamines: 5-BZT-MDA 5-BZT-MDMA 6-BZT-MDA 6-BZT-MDMA Benzoxathioles Amphetamines:
3,4-Ethylenedioxymethcathinone
3,4-Ethylenedioxymethcathinone
Pharmaceutical compound
serotonin 5-HT1A, 5-HT2B, 5-HT6, and 5-HT7 receptors, and an agonist of the serotonin 5-HT1D and 5-HT2C receptors. Similarly to tryptamine and 5-MeO-T, but
5-Methyltryptamine
Chemical compound
LY-293284, also known as 4,α-methylene-5-acetyl-DPT, is a research chemical developed by the pharmaceutical company Eli Lilly and used for scientific
LY-293284
Class of compounds based upon the amphetamine structure
Synthesized Chemicals and Psychoactive Plants (First ed.). John Wiley & Sons. p. 5. ISBN 9781118106051. Retrieved 16 February 2019. PubChem. "Phenylpropanolamine"
Substituted_amphetamine
Serotonin receptor protein distributed mainly in the choroid plexus
The 5-HT2C receptor is a subtype of the 5-HT2 receptor that binds the endogenous neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). Like all 5-HT2
5-HT2C_receptor
Chemical compound
5,N-Dimethyl-N-isopropyltryptamine (5-Me-MiPT) is a tryptamine derivative that is thought to be a psychedelic drug. It was first made in 1989. In vitro
5-Me-MiPT
Weight loss medication
PMC 6623861. PMID 22114263. Reyes-Parada M, Iturriaga-Vasquez P, Cassels BK (2019). "Amphetamine Derivatives as Monoamine Oxidase Inhibitors". Frontiers
Phentermine
Drug class
A serotonin 5-HT2A receptor antagonist, or simply 5-HT2A antagonist, is a drug which acts as an antagonist of the serotonin 5-HT2A receptor. Aside from
Serotonin 5-HT2A receptor antagonist
Serotonin_5-HT2A_receptor_antagonist
Atypical antipsychotic
adjunctive therapy with an oral antidepressant. The most common adverse effects (≥5%) were somnolence and dry mouth. Lumateperone is associated with a low rate
Lumateperone
Chemical compound
into 5-hydroxytryptophan (5-HTP) which is then converted into the neurotransmitter serotonin, it has been proposed that consumption of tryptophan or 5-HTP
Tryptophan
Chemical compound of the cathinone class
5-Methoxymethylone (also known as 2-A1MP and βk-MMDMA) is a chemical compound of the cathinone class which has been sold online as a designer drug. It
5-Methoxymethylone
Designer drug combination mimicking MDMA
Yamamoto BK, Nash JF (November 1994). "Potentiation of 3,4-methylenedioxymethamphetamine-induced dopamine release and serotonin neurotoxicity by 5-HT2 receptor
Borax_combo
Colourless non-flammable greenhouse gas
America Journal. 75 (5): 1829. Bibcode:2011SSASJ..75.1829M. doi:10.2136/SSSAJ2010.0415. Molodovskaya M, Singurindy O, Richards BK, Warland JS, Johnson
Nitrous_oxide
Class of transmembrane proteins
Cassels BK, Huidobro-Toro JP (April 2004). "4-Bromo-2,5-dimethoxyphenethylamine (2C-B) and structurally related phenylethylamines are potent 5-HT2A receptor
5-HT_receptor
Chemical compound
5-MAPDB, also known as 5-(2-(methylamino)propyl)-2,3-dihydrobenzofuran, is an entactogen of the dihydrobenzofuran family. It is structurally related to
5-MAPDB
Serotonin modulator antidepressant
agonist of the serotonin 5-HT1A receptor, partial agonist of the 5-HT1B receptor, and antagonist of the serotonin 5-HT1D, 5-HT3, and 5-HT7 receptors, as well
Vortioxetine
Pharmaceutical compound
4-F-5-MeO-pyr-T, also known as 4-fluoro-5-methoxy-N,N-pyrrolidinyltryptamine, is a serotonin 5-HT1A receptor agonist of the tryptamine and pyrrolidinylethylindole
4-F-5-MeO-pyr-T
Monoamine neurotransmitter
serotonin 5-HT1 (1A, 1B, 1D, 1E, 1F), 5-HT2 (2A, 2B, 2C), 5-HT3, 5-HT4, 5-HT5 (5A, 5B), 5-HT6, and 5-HT7 receptors. Except for the serotonin 5-HT3 receptor
Serotonin
Medication used for the treatment of migraine headaches
taken by mouth. It can also be applied on the tongue. It is a serotonin (5-HT) 1B/1D receptor agonist (triptan). Common side effects include chest pain
Rizatriptan
Muscle relaxant medication
serotonin–norepinephrine reuptake inhibition, serotonin 5-HT2A, 5-HT2B, 5-HT2C, 5-HT6, and 5-HT7 receptor antagonism, α1- and α2-adrenergic receptor antagonism
Cyclobenzaprine
Chemical compound
1-Aminomethyl-5-methoxyindane (AMMI), is a drug developed by a team led by David E. Nichols at Purdue University, which acts as a selective serotonin
1-Aminomethyl-5-methoxyindane
Chemical compound
moderately selective full agonist at the 5-HT3 receptor. 5-Carboxamidotryptamine 5-Methoxytryptamine α-Methyl-5-hydroxytryptamine Elz S, Zimmermann H, Rehse
2-Methyl-5-hydroxytryptamine
Serotonin receptor protein distributed in the cerebrum and raphe nucleus
receptor (or 5-HT1A receptor) is a subtype of serotonin receptors, or 5-HT receptors, that binds serotonin, also known as 5-HT, a neurotransmitter. 5-HT1A is
5-HT1A_receptor
Atypical antipsychotic medication
Serotonin 5-HT1A receptor partial agonist, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT3, 5-HT6, and 5-HT7 receptor antagonist, and 5-HT1B, 5-HT1D, 5-HT1E, and 5-HT1F receptor
Quetiapine
Pharmacodynamics and pharmacokinetics of ethanol
Voltage-gated calcium channel Dihydropyridine-sensitive L-type Ca2+ channels BK channel modulation G-protein-activated inwardly rectifying K+ channels Brain
Pharmacology_of_ethanol
Serotonin antagonist
AZ10419369 Benzofurans (e.g., 5-MAPB, 6-MAPB, BK-5-MAPB, BK-6-MAPB) Benzothiophenes (e.g., 5-MAPBT, 6-MAPBT, BK-5-MAPBT) CGS-12066 (CGS-12066A, CGS-12066B)
Tipindole
Pharmaceutical compound
BK-5Cl-NM-AMT, or βk-5Cl-NM-αMT, also known as β-keto-5-chloro-N-methyl-αMT or α,N-dimethyl-5-chloro-β-ketotryptamine, is a monoamine releasing agent
BK-5Cl-NM-AMT
Antidepressant medication
Side Effects. John Wiley & Sons. pp. 149–. ISBN 978-3-527-62147-7. Logan BK, Costantino AG, Rieders EF, Sanders D (November 2010). "Trazodone,
Trazodone
Pharmaceutical compound
5-Allyloxy-AMT, also known as 5-allyloxy-α-methyltryptamine, is a serotonin 5-HT2 receptor agonist of the tryptamine, 5-alkyloxytryptamine, and α-alkyltryptamine
5-Allyloxy-AMT
Medication mainly used for depression and smoking cessation
by as much as 5.5 times (with a half-life of 12–30 hours), while the effective doses of hydroxybupropion may differ by as much as 7.5 times (with a half-life
Bupropion
Chemical compound
5-(Nonyloxy)tryptamine (5-NOT) is a tryptamine derivative which acts as a selective agonist at the 5-HT1B receptor. Increasing the O-alkoxy chain length
5-(Nonyloxy)tryptamine
Drug class
5-HT2C receptor agonists are a class of drugs that activate 5-HT2C receptors. They have been investigated for the treatment of a number of conditions
5-HT2C_receptor_agonist
Pharmaceutical compound
It is the 5-chloro derivative of tryptamine. The drug shows affinity for the serotonin 5-HT1A, 5-HT2A, 5-HT6, and 5-HT7 receptors (Ki = 5.5–16 nM, 317–889 nM
5-Chlorotryptamine
Transmembrane protein
5-HT2B receptor 5-HT2C receptor 5-HT1 receptor 5-HT3 receptor 5-HT4 receptor 5-HT5 receptor 5-HT6 receptor 5-HT7 receptor Category:5-HT2 antagonists Hoyer
5-HT2_receptor
Pharmaceutical compound
synthesis of 5-MeO-MBT has been described. 5-MeO-MBT has several possible positional isomers, including 5-MeO-MiBT, 5-MeO-MsBT, and 5-MeO-MtBT. 5-MeO-MBT was
5-MeO-MBT
Common name for more than 1,000 species of flowering plants in the family Convolvulaceae
related species, are significantly more potent, typically requiring only 5–10 seeds. For optimal effects, seeds from any species should ideally be ground—rather
Morning_glory
Pharmaceutical compound
5-Fluorotryptamine (5-fluoro-T, 5-FT, or 5-F-T; code name PAL-284) is a serotonin receptor agonist and monoamine releasing agent of the tryptamine family
5-Fluorotryptamine
DMT-infused smoking blend
caapi vine and/or leaf 20% mullein 20% passionflower 20% peppermint 5% calendula 5% blue lotus Palmer has noted that while many herbs can be used, the
Changa_(drug)
Phytocannabinoid discovered in 1940
4/unsworks_50076. PMID 29511052. Elliott J, DeJean D, Clifford T, Coyle D, Potter BK, Skidmore B, et al. (February 2020). "Cannabis-based products for pediatric
Cannabidiol
Medication used for migraines & cluster headaches
Sumatriptan is a serotonin (5-HT1B/1D) receptor agonist (triptan). The drug acts as a serotonin 5-HT1B, 5-HT1D, and 5-HT1F receptor agonist and its
Sumatriptan
Medication mainly used to treat gout
cardiovascular diseases. As an anti-inflammatory drug, Lodoco in a dose of 0.5 mg per day reduced the rate of cardiovascular events by 31% in people with
Colchicine
Chemical class of organic compounds
glaucine, and nuciferine Others like 6-AB, 2-ADN, 2C-B-PYR, 2C-B-5-hemiFLY-α6 (BNAP), 2CB7 (2C-B-5-hemiFLY-β7), 2CBecca, 2CJP, 2CLisaB, 2CLisaH, 2-naphthylamine
Substituted_phenethylamine
Chemical compound
MEAI, also known as 5-methoxy-2-aminoindane (5-MeO-AI) and by its developmental code name CMND-100, is an entactogen-like psychoactive drug of the 2-aminoindane
MEAI
Pharmaceutical compound
1-Methylmedmain, also known as 1,2-dimethyl-3-ethyl-5-dimethylaminoindole, is a serotonin receptor modulator and indole derivative related to the neurotransmitter
1-Methylmedmain
Anti-nausea group of medications
The 5-HT3 antagonists, informally known as "setrons", are a class of drugs that act as receptor antagonists at the 5-HT3 receptor, a subtype of serotonin
5-HT3_antagonist
Dopamine agonist medication
224. Washington, D.C.: American Chemical Society. pp. 201–222. doi:10.1021/bk-1983-0224.ch009. ISBN 978-0-8412-0781-3. The situation seems further confounded
Ropinirole
Beta blocker drug
relatively weak antagonist of certain serotonin receptors, namely the 5-HT1A, 5-HT1B, and 5-HT2B receptors. The latter may be involved in the effectiveness
Propranolol
Designer drug of the cathinone class
Eutylone (also known as β-keto-1,3-benzodioxolyl-N-ethylbutanamine, bk-EBDB, and N-ethylbutylone) is a stimulant and empathogenic drug of the phenethylamine
Eutylone
Chemical compound
CJ-033466 is a drug which acts as a potent and selective 5-HT4 serotonin receptor partial agonist. In animal tests it stimulated gastrointestinal motility
CJ-033466
Synthetic opioid pain medication
α2-adrenergic receptor antagonists such as yohimbine, the 5-HT3 receptor antagonist ondansetron, and the 5-HT7 receptor antagonists SB-269970 and SB-258719. Pharmacologically
Tramadol
Pharmaceutical compound
ISSN 0009-2665. Retrieved 9 January 2026. Gornez-Jeria JS, Morales-Lagos D, Cassels BK, Saavedra-Aguilar JC (1986). "Electronic Structure and Serotonin Receptor
S-DMT
Chemical compound
(MY400) 6-APBT 6-MAPBT (MY300) 7-APBT Cathinones: BK-5-MAPBT Benzothiazoles Amphetamines: 5-BZT-MDA 5-BZT-MDMA 6-BZT-MDA 6-BZT-MDMA Benzoxathioles Amphetamines:
MDAT
Antihistamine medication
Diphenhydramine is not known to bind to the 5-HT2A receptor, though it is a weak antagonist of the related 5-HT2C receptor, which is another target of antidepressant
Diphenhydramine
Protein-coding gene in the species Homo sapiens
5-hydroxytryptamine (serotonin) 1E receptor (5-HT1E) is a highly expressed human G-protein coupled receptor that belongs to the 5-HT1 receptor family
5-HT1E_receptor
Pharmaceutical compound
chemical structure of MYCO-006 does not yet appear to have been disclosed. 5-BZT-MDMA and 6-BZT-MDMA were described in Mydecine's patent for short-acting
MYCO-006
Chemical compound
5-Methyl-MDA, also known as 5-methyl-3,4-methylenedioxyamphetamine, is an entactogen and psychedelic designer drug of the amphetamine class. It is a ring-methylated
5-Methyl-MDA
Pharmaceutical compound
5-Methoxyharmalan, also known as 5-methoxy-1-methyl-4,9-dihydro-3H-β-carboline, is a serotonin receptor modulator of the β-carboline family. It is a cyclized
5-Methoxyharmalan
Pharmaceutical compound
5-DM-25B-NBOMe, also known as 5-O-desmethyl-25B-NBOMe, is a serotonin receptor modulator of the phenethylamine family related to the NBOMe psychedelic
5-DM-25B-NBOMe
Ionotropic serotonin receptor
The 5-HT3 receptors are a subclass of serotonin (5-HT) receptors. They belong to the Cys-loop superfamily of ligand-gated ion channels (LGICs) and differ
5-HT3_receptor
Medication for nausea, psychosis, and anxiety
[104-16-5] (2) in the presence of sodamide gives Prochlorperazine (3); or by alkylation of 2-Chloro-10-(3-chloropropyl)phenothiazine [2765-59-5] (4) and
Prochlorperazine
Species of amphibian
Incilius alvarius. The Colorado River toad can grow to about 190 millimetres (7.5 in) long and is the largest toad in the United States apart from the non-native
Colorado_River_toad
MDMA analogue
they are less potent and efficacious in activating the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors than MDMA and show differing and potentially improved
SeDMA
Pharmaceutical compound
Transporter Activities (Abstract ID: 228967)". The Journal of Pharmacology and Experimental Therapeutics. 393 (5) 104084. doi:10.1016/j.jpet.2026.104084.
D2-MDMA
Chemical compound
5-APDB, also known as 5-(2-aminopropyl)-2,3-dihydrobenzofuran or as 3-desoxy-MDA, is an entactogen of the phenethylamine, amphetamine, and dihydrobenzofuran
5-APDB
travel, tourism, insurance
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
BK 5-MAPBT
travel, tourism, insurance