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Chemical compound
5-MAPB, also known as 5-(N-methyl-2-aminopropyl)benzofuran, as well as by nicknames such as "MDMA 2.0" and "Gas Station Molly", is an entactogen of the
5-MAPB
Designer drug combination mimicking MDMA
mixture of the entactogen 5-MAPB or MDAI, the stimulant 2-fluoromethamphetamine (2-FMA), and the serotonergic psychedelic 5-MeO-MiPT or 4-HO-MET, all
Borax_combo
Chemical compound
βk-5-MAPB, or BK-5-MAPB, is an entactogen of the benzofuran and cathinone groups which is related to both 5-MAPB and methylone. It was patented by Matthew
BK-5-MAPB
Class of psychoactive drugs that produce empathic experiences
MDMA, MDA, MDEA, MDOH, MBDB, and methylone, the benzofurans 5-APB, 5-MAPB, 6-APB, and 6-MAPB, the cathinone mephedrone, the 2-aminoindane MDAI, and the
Entactogen
Chemical compound
to produce similar effects. Substituted benzofuran 5-MAPB, 5-APB, and 6-APB BK-5-MAPB and BK-6-MAPB TACT411 and TACT833 Oeri HE (May 2021). "Beyond ecstasy:
6-MAPB
Psychoactive drug, often called ecstasy
MDEA, 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
MDMA
Chemical compound
described as the benzofuran-5-yl analogue of MBDB or the butanamine homologue of 5-MAPB, and is also a structural isomer of 5-EAPB and 6-EAPB. Anecdotal
5-MBPB
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
Chemical compound
2-MAPB is a recreational designer drug with empathogenic effects. As with other related substituted benzofuran derivatives such as 6-APB and 5-MAPB, 2-MAPB
2-MAPB
Chemical compound
structurally related to drugs like 5-APDB and 5-MAPB, which have similar effects to MDMA and have been used as recreational drugs. 5-MAPDB has been studied to
5-MAPDB
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
Central nervous system stimulant prodrug
earliest for d-MPH-ER at 0.5 hours, followed by d, l-MPH-LA at 1 to 2 hours, MCD at 1.5 hours, d, l-MPH-OR at 1 to 2 hours, MAS-XR at 1.5 to 2 hours, MTS at 2
Lisdexamfetamine
Class of chemical compounds
agents and as serotonin 5-HT2 receptor agonists. In addition, some benzofurans, including 5-MAPB, 6-MAPB, BK-5-MAPB, and BK-6-MAPB, have unexpectedly been
Substituted_benzofuran
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
Pharmaceutical compound
BK-5-MAPBT has been studied and patented by Matthew J. Baggott of Tactogen. Substituted benzothiophene Substituted cathinone 5-MAPBT BK-5-MAPB WO 2022010937A1
BK-5-MAPBT
Central nervous system stimulant
methamphetamine at doses 5–10 mg/day for ADHD in adults and children over six years of age, which may be increased at weekly intervals of 5 mg, up to 25 mg/day
Methamphetamine
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
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
Chemical compound
5-MAPDI (also known as Indanylmethylaminopropane or IMP) is an entactogenic amphetamine derivative which is structurally related to MDMA as well as to
5-MAPDI
Weight loss medication
inactive as a ligand or agonist of the serotonin 5-HT2 receptors, including of the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors. This is in contrast to the
Phentermine
Chemical compound
plasma is reached. The mean residence time is 5.2 ± 3.4 hours. The elimination half-life of cathinone is 1.5 ± 0.8 hours. A two-compartment model for absorption
Cathinone
Chemical compound
phenethylamine, amphetamine, and benzothiophene families. It is closely related to 5-MAPB, but with the oxygen atom replaced by sulfur, changing the core ring structure
5-MAPBT
Topical nasal decongestant
single intravenous doses of 0.25 to 0.5 mg/kg. The volume of distribution of levomethamphetamine is 288.5 to 315.5 L or 4.15 to 4.17 L/kg. The pharmacokinetics
Levomethamphetamine
Compounds that damage or destroy monoaminergic neurons
4-Chlorophenylisobutylamine (4-CAB; 4-chloro-α-desmethyl-α-ethylamphetamine; α-ethyl-PCA) 5-MAPB Fenfluramine Mephedrone Methamphetamine Methylbenzodioxolylbutanamine (MBDB)
Monoamine_neurotoxin
Medication used to treat dyskinesia
catecholamines and serotonin in the brain". Bioorg Med Chem. 9 (5): 1197–1212. doi:10.1016/s0968-0896(01)00002-5. PMID 11377178. Knoll J, Yoneda F, Knoll B, Ohde H
Amantadine
Heterocyclic compound consisting of fused benzene and furan rings
herbicides: ethofumesate and benfuresate. Several psychoactive drugs such as 5-MAPB and 6-APB are also derived from benzofuran. Benzofuran is extracted from
Benzofuran
Synthetic decongestant
average is 5.4 hours and ranges from 3 to 16 hours depending on urinary pH. At a pH of 5.6 to 6.0, the elimination half-life of pseudoephedrine was 5.2 to 8
Pseudoephedrine
Codrug of amphetamine and theophylline
captagon seizures estimated the drug's entire market to be worth at least $5.7bn. Smuggling of fenethylline became Syria's principal export, exceeding
Fenethylline
Naturally occurring psychedelic compound
agonist at serotonin 5-HT2A receptors, with varying affinity and efficacy across multiple other receptors and targets. The serotonin 5-HT2A receptor antagonist
Mescaline
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
Trace amine
effects of exercise?". British Journal of Sports Medicine. 35 (5): 342–343. doi:10.1136/bjsm.35.5.342. PMC 1724404. PMID 11579070. The 24 hour mean urinary
Phenethylamine
CNS stimulant and isomer of amphetamine
Retrieved 5 January 2017. "ProCentra (dextroamphetamine sulfate 5 mg/5 mL Oral Solution)". FSC Laboratories. Archived from the original on 5 October 2010
Dextroamphetamine
Subtype of serotonin receptor
The 5-HT2A receptor is a subtype of the 5-HT2 receptor that belongs to the serotonin receptor family and functions as a G protein-coupled receptor (GPCR)
5-HT2A_receptor
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
Decongestant medication
contraindication to phenylephrine use. As a mydriatic, it is available in 2.5% and 10% eye drops. Phenylephrine eye drops are applied to the eye after a
Phenylephrine
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
Recreational drug
significant affinity for various receptors, including the serotonin 5-HT2A, 5-HT2B, 5-HT2C, and α2-adrenergic receptors, as well as the trace amine-associated
Mephedrone
Chemical compound
structurally related to 5-MAPB and 5-APB. It might be predicted to show similar effects to these drugs in humans, but the pharmacology of 5-EAPB remains unstudied
5-EAPB
Pharmaceutical compound
profile of acting as full versus partial releasers. Unlike 5-MAPB, it is a relatively weak serotonin 5-HT1B receptor agonist. 6-MBPB partially substituted for
6-MBPB
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
Sympathomimetic agent
administration. Immediate-release forms of the drug reached peak levels about 1.5 hours (range 1.0 to 2.3 hours) following administration. Conversely, extended-release
Phenylpropanolamine
Chemical compound
acute overdosage. The LD50 for methylhexanamine is 39 mg/kg in mice and 72.5 mg/kg in rats, when administered intravenously. The FDA has stated that methylhexanamine
Methylhexanamine
American businessman
Transcend), which are all close psilocin analogues, as well as the entactogen 5-MAPB (Plür). According to Weiss, the United States Federal Analogue Act, which
Judd_Weiss
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
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, stimulant and decongestant
available over-the-counter in the form of 12.5 and 25 mg oral tablets for use as a bronchodilator and as a 0.5% concentration nasal spray for use as a decongestant
Ephedrine
Pharmaceutical compound
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
Isocyclamine
Antipsychotic medication
basis. It has actions at several 5-HT (serotonin) receptor subtypes. These are 5-HT2C, linked to weight gain, and 5-HT2A, linked to its antipsychotic
Risperidone
Drug class
genetic polymorphism of the enzyme CYP450 2D6. Under normal conditions, around 5 to 30% of amphetamine is excreted unchanged in the urine. However, the urinary
Norepinephrine–dopamine releasing agent
Norepinephrine–dopamine_releasing_agent
Substituted cathinone designer drug
properties compared to mephedrone or MDMA. 3-MMC binds to serotonin 5-HT1A, 5-HT2A, and 5-HT2C receptors, although it is unknown what impact this activity
3-Methylmethcathinone
Chemical compound
5-Methoxytryptamine (5-MT, 5-MeO-T, or 5-OMe-T), also known as serotonin methyl ether or O-methylserotonin and as mexamine, is a tryptamine derivative
5-Methoxytryptamine
Withdrawn anti-obesity drug combination
it only temporarily reduced weight. A 1984 study found a weight loss of 7.5 kg on average in 24 weeks, as compared to 4.4 kg under placebo. It sold modestly
Fenfluramine/phentermine
Chemical compound
intravenous use. It is supposedly active at doses of 3 to 5 mg, with typical doses ranging between 5 and 20 mg. The long-term effects of MDPV on humans have
Methylenedioxypyrovalerone
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
Class of compounds
(MDMA) 5-(2-Aminopropyl)benzofuran (5-APB) 5-(2-Aminopropyl)-2,3-dihydrobenzofuran (5-APDB) 5-Indanyl-2-aminopropane (IAP) 5-MABB 5-MAPB 6-(2-Aminopropyl)benzofuran
Serotonin_releasing_agent
Psychoactive substance found in plants in the family Apocynaceae
blocked by the serotonin 5-HT2 receptor antagonist metergoline. The preceding findings suggest that serotonin 5-HT2A and 5-HT2C receptor activation are
Ibogaine
Typical antipsychotic medication
associated with extrapyramidal side effects. Doses of haloperidol greater than 5 mg increased the risk of side effects without improving efficacy. Patients
Haloperidol
Pharmaceutical compound
4-Dimethylamylamine (1,4-DMAA), also known as 1,4-dimethylpentylamine or as 5-methylhexan-2-amine, is a stimulant drug of the alkylamine family related
1,4-Dimethylamylamine
Chemical compound
N-Ethyl-5-trifluoromethyl-2-aminoindane (ETAI) is a drug of the 2-aminoindane family with putative entactogenic effects. It functions as a serotonin releasing
Ethyltrifluoromethylaminoindane
Ethyltrifluoromethylaminoindane
Chemical compound
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
Cypenamine
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
Type of drug
methamphetamine (in high doses), certain substituted benzofurans such as 5-APB and 6-APB, naphthylisopropylamine; cathinones such as mephedrone and methylone;
Serotonin–norepinephrine–dopamine releasing agent
Serotonin–norepinephrine–dopamine_releasing_agent
Chemical compound
α-methylserotonin (5-HO-AMT), 5-EtO-AMT, 5-AlO-AMT, 5-fluoro-AMT, 5-chloro-AMT, α,N,O-TMS (5-MeO-N-Me-AMT), α,N,N,O-TeMS (5-MeO-α,N,N-TMT), 5-MeO-DMT, 5-MeO-DPT, 5-MeO-DiPT
5-MeO-AMT
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
Atypical antipsychotic medication
as a partial agonist at dopamine D3 and D4 receptors and at serotonin 5-HT1A and 5-HT2C receptors. It is a third-generation antipsychotic and its introduction
Aripiprazole
Atypical antipsychotic medication
gradually increased over a number of weeks. Initial doses may range from 6.5 to 12.5 mg/d, increasing stepwise typically, to doses in the range of 250–350 mg
Clozapine
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 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 found in some species of mushrooms
serotonin receptors. Activation of one serotonin receptor, the serotonin 5-HT2A receptor, is specifically responsible for the hallucinogenic effects
Psilocybin
Pharmaceutical compound
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
3F-Thozalinone
Blood pressure medication
β2-adrenergic receptor, α1-adrenergic receptor, α2-adrenergic receptor, 5-HT1A receptor, 5-HT2 receptor, H1 receptor, D2 receptor, μ-opioid receptor, veratridine
Carvedilol
Trace amine
behavior in locust phase changes". Scientific Reports. 5 (1). Nature/Springer: 8036. Bibcode:2015NatSR...5.8036M. doi:10.1038/srep08036. PMC 5389030. PMID 25623394
Tyramine
Atypical antipsychotic medicine
receptor. It is a partial agonist at the serotonin 5-HT1A receptor and acts as an antagonist at 5-HT2B and 5-HT2A receptors. It is taken by mouth. The most
Cariprazine
Psychedelic drug
the serotonin 5-HT2A receptor among others. The drug produces its hallucinogenic effects specifically via activation of the serotonin 5-HT2A receptor
Psilocin
Type of drug
MDMA and mephedrone, and serotonin–dopamine releasing agents (SDRAs) like 5-chloro-αMT and BK-NM-AMT, are known. A closely related type of drug is a dopamine
Dopamine_releasing_agent
Chemical compound
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
Clominorex
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
Stimulant drug of the phenethylamine class
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
4-Methylphenylisobutylamine
Pharmaceutical compound
2-Methyl-MDA pCPE 4-CAB 4-FA 4-FMA 4-HA 4-MTA 4-ME 5-APB 5-APBT 5-APDB 5-MAPB 5-Methyl-MDA 6-APB 6-APBT 6-APDB 6-MAPB 6-Methyl-MDA AEMMA Amiflamine BDB BOH Brephedrone
Octodrine
6-(2-Aminopropyl)benzofuran (6-APB) 5-(2-Aminopropyl)benzofuran (5-APB) 5-(2-Methylaminopropyl)benzofuran (5-MAPB) 5-APDI (indanylaminopropane; IAP)[citation
List_of_entactogens
Antidepressant medication
serotonin 5-HT2A and 5-HT2C receptor antagonist, but has about 15-fold greater potency as an antagonist of the 5-HT2A receptor relative to the 5-HT2C receptor
Trazodone
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
Pharmaceutical compound
comedown after MDMA, it was found that MDMA produced acute cognitive deficits 5 and 26 hours after administration and the deficits could be prevented by citalopram
MDMA/citalopram
Class of chemical compounds
βk-2C-B, appear to show dramatically reduced potency and efficacy as serotonin 5-HT2A receptor agonists compared to their non-β-keto-substituted counterparts
Substituted_cathinone
Typical antipsychotic medication
nigrostriatal system produces the extrapyramidal effects Serotonin receptors (5-HT2, 5-HT6 and 5-HT7), with anxiolytic, antidepressant and antiaggressive properties
Chlorpromazine
Psychoactive stimulant
for monoamine transporters in brain tissue". Neuropsychopharmacology. 37 (5): 1192–1203. doi:10.1038/npp.2011.304. PMC 3306880. PMID 22169943. Blough
Methcathinone
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
Pharmaceutical compound
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
Phenylbutynamine
Stimulant designer drug of the substituted cathinone class
4-FA 4-FMA 4-MA 4-MMA 4-MTA 5-APB 5-APBT 5-APDB 5-EAPB 5-IT 5-MAPB 5-MAPDB 6-APB 6-APDB 6-APBT 6-Chloro-MDMA 6-EAPB 6-IT 6-MAPB 6-MAPDB EDA IAP 2,3-MDA 3
2-Methylmethcathinone
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
Chemical compound
Comparison of the DA, 5-HT, and NE Releasing Activity of a Series of Phenmetrazine Analogs [...] Table 5. Comparison of the DA, 5-HT, and NE Releasing
Phenmetrazine
Entactogen drug
serotonin 5-HT1A, 5-HT1B, and 5-HT1D receptors. In contrast to MDMA however, methylone and its metabolites lack significant affinity for the serotonin 5-HT2A
Methylone
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
Drug class
Phenethylamines: 2-OH-PEA 4-CAB 4-FA 4-FMA 4-MA 4-MMA 5-APB 5-APBT 5-MAPB 6-APB 6-APBT 6-MAPB Alfetamine Amfecloral Amfepentorex Amfepramone Amphetamine
Serotonin–norepinephrine releasing agent
Serotonin–norepinephrine_releasing_agent
Chemical compound
Chromatography of Pure Adrenochrome". Canadian Journal of Chemistry. 36 (5): 853–857. Bibcode:1958CaJCh..36..853H. doi:10.1139/v58-124. Tamou Thahouly
Adrenochrome
SSRI antidepressant
June 2019. p. 5. Retrieved 19 July 2023. "SSRIs, SNRIs: risk of persistent sexual dysfunction". Reactions Weekly. 1838 (5). Springer: 5. 16 January 2021
Fluoxetine
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
Chemical compound
5-Fluoro-AET, also known as 5-fluoro-α-ethyltryptamine or by the code name PAL-545, is a substituted tryptamine derivative which acts as a serotonin–dopamine
5-Fluoro-AET
Chemical compound
2-Methyl-MDA pCPE 4-CAB 4-FA 4-FMA 4-HA 4-MTA 4-ME 5-APB 5-APBT 5-APDB 5-MAPB 5-Methyl-MDA 6-APB 6-APBT 6-APDB 6-MAPB 6-Methyl-MDA AEMMA Amiflamine BDB BOH Brephedrone
1,3-Dimethylbutylamine
Psychedelic drug
drug acts as a potent partial agonist of the serotonin 5-HT2 receptors, including of the serotonin 5-HT2A receptor. It produces psychedelic-like effects
2C-B
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5 MAPB
5 MAPB
5 MAPB
5 MAPB
5 MAPB
5 MAPB
5 MAPB
5 MAPB
5 MAPB
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