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Chemical compound
5-(2-Aminopropyl)-2,3-dihydro-1H-indene (5-APDI), also known as indanylaminopropane (IAP), 2-aminopropylindane (2-API), indanametamine, and, incorrectly
5-APDI
Class of psychoactive drugs that produce empathic experiences
(MDxx) 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
Entactogen
Chemical compound
serotonin 5-HT1B, 5-HT2A, 5-HT2B, and 5-HT2C receptors. Some notable analogues of 5-MAPB besides MDMA include other benzofurans like 5-APB, 5-MAPDB, and
5-MAPB
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
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
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
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
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
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-MAPDI (also known as Indanylmethylaminopropane or IMP) is an entactogenic amphetamine derivative which is structurally related to MDMA as well as to
5-MAPDI
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
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
Chemical compound
List of aminorex analogues US 3321470, Howell Jr CF, Hardy RA, Quinones N, "5-Arylidene-2-Amino-2-Oxazolin-4-Ones", issued 23 May 1967, assigned to American
Cyclazodone
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
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
Chemical compound
amphetamine: 2-amino-1,2-dihydronaphthalene". Journal of Medicinal Chemistry. 25 (5): 535–538. doi:10.1021/jm00347a011. PMID 6123601. "1-Phenylpiperazine". pubchem
Phenylpiperazine
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
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
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
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
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
Psychedelic drug
receptors: 5-HT1A, 5-HT1B, 5-HT1D, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT6, and 5-HT7. An agonist action has been determined at 5-HT1A, 5-HT2A and 5-HT2C. Its efficacies
Dimethyltryptamine
Pharmaceutical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Isocyclamine
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
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
Pharmaceutical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
2-APB_(entactogen)
Group of stereoisomers
4-Methylaminorex (4-MAR, 4-MAX) is a stimulant drug of the 2-amino-5-aryloxazoline group that was first synthesized in 1960 by McNeil Laboratories. It
4-Methylaminorex
Drug mixture used mainly to treat ADHD and narcolepsy
amphetamine treatment for ADHD in children that found an average increase of 4.5 IQ points, continued increases in attention, and continued decreases in disruptive
Adderall
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
Decongestant and stimulant drug
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Cyclopentamine
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
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
Pharmaceutical compound
exhibit differential effects on synaptosomal release of 3H-dopamine and 3H-5-hydroxytryptamine". Pharmacol Biochem Behav. 38 (3): 505–512. doi:10
Homo-MDMA
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
Pharmaceutical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Octodrine
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
Mammalian protein found in humans
The serotonin transporter (SERT or 5-HTT), also known as the sodium-dependent serotonin transporter and solute carrier family 6 member 4, is a protein
Serotonin_transporter
Drug class
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Serotonin–norepinephrine releasing agent
Serotonin–norepinephrine_releasing_agent
Medication
placebo decreased scores by 6.5 to 8.6 points, giving placebo-subtracted differences attributable to selegiline of 2.4 to 2.5 points. A 2013 quantitative
Selegiline
Psychoactive drug, often called ecstasy
the serotonin 5-HT1 receptors, including the serotonin 5-HT1A, 5-HT1B, and 5-HT1D receptors, and is a partial agonist of the serotonin 5-HT2 receptors
MDMA
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
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
Sympathomimetic agent
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Tuaminoheptane
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
Chemical compound
norepinephrine, with an EC50 of 109 nM (DA), 41.4 nM (NE), and 5,246 nM (5-HT). It also functions as a weak monoamine oxidase inhibitor (MAOI) (IC50Tooltip
4-Benzylpiperidine
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
Serotonin_releasing_agent
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
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
Topical nasal decongestant
adults and children 6–12 years of age. Each inhalation delivers 0.4 to 0.5 mg (400 to 500 μg) in 800 mL of air. Use is not to exceed three days. Historically
Propylhexedrine
Chemical compound
5-EAPB, also known as 5-(2-(ethylamino)propyl)benzofuran, is a potentially entactogenic amphetamine and benzofuran which is structurally related to 5-MAPB
5-EAPB
Group of stereoisomers
Fluminorex Pemoline Thozalinone DE 1297108, Beil W, Hoeppener A, Wolff HJ, "5-phenyl-2-ethylamino-4-oxazolinone and its preparation", issued 12 June 1969
Fenozolone
Pharmaceutical compound
predicted to interact with the monoamine transporters and with the serotonin 5-HT2 receptors. In contrast to MDMA, it does not produce hyperthermia in rodents
APA-01
Chemical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
1,3-Dimethylbutylamine
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
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
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Methylenedioxybenzylpiperazine
Methylenedioxybenzylpiperazine
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
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
Chemical compound
time-dependent hypothermia. MBDB has similar affinities for the serotonin 5-HT1A and 5-HT2A receptors as MDMA. However, MBDB did not show the head-twitch response
MBDB
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
Stimulant designer drug of the substituted cathinone class
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
2-Methylmethcathinone
Chemical compound
Games among other athletic events) bans cathine in concentrations of over 5 micrograms per milliliter in urine. Cathine is a Schedule III drug under the
Cathine
Chemical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Methylbenzylpiperazine
Chemical compound
notably includes the serotonin 5-HT2A receptor, which is implicated in producing psychedelic effects, and the serotonin 5-HT2B receptor, which is implicated
MDAI
Pharmaceutical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Phenylbutynamine
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
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
Proteins that function as integral plasma-membrane transporters
angiotensin II. SERT is responsible for the reuptake of extracellular serotonin (5-HT) in a Na +/Cl − -dependent process. In the CNS, SERT is found localized
Monoamine_transporter
Chemical compound
and 5-methoxy-6-methyl-2-aminoindan: similarities to 3,4-(methylenedioxy)methamphetamine (MDMA)". Journal of Medicinal Chemistry. 34 (5): 1662–8
6-CAT
Entactogen drug
(3T-MDMA; MY100) MY101 MY200 Indanes Amphetamines: 5-APDI (IAP) 5-MAPDI (IMP) Indoles Amphetamines: 5-API (5-IT; PAL-571) 6-API (6-IT) Naphthalenes Amphetamines:
MDMAT
Psychoactive drug and research chemical
(3T-MDMA; MY100) MY101 MY200 Indanes Amphetamines: 5-APDI (IAP) 5-MAPDI (IMP) Indoles Amphetamines: 5-API (5-IT; PAL-571) 6-API (6-IT) Naphthalenes Amphetamines:
4-Bromomethcathinone
Pharmaceutical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Phenylpropylamine
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
Psychedelic tryptamine
4-MeO-DiPT, 5-HO-DiPT, 5-MeO-DMT, 5-MeO-DET, 5-MeO-DPT, 5-MeO-DALT, 5-MeO-MiPT, 5-MeO-MsBT, 5-MeO-EiPT, 5-MeO-PiPT, 5-MeO-iPALT (ASR-3001), and 5-MeO-DiBF
5-MeO-DiPT
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
1991 book by Alexander Shulgin and Ann Shulgin
(3-methyl-DOM) Hecate (DOET; 4-desmethyl-4-ethyl-DOM) Iris (5-desmethoxy-5-ethoxy-DOM; DOM-5-EtO) Juno (6-methyl-DOM) As with the essential amphetamines
PiHKAL
Anorectic stimulant drug
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Amfepentorex
Pharmaceutical compound
228563)". The Journal of Pharmacology and Experimental Therapeutics. 393 (5) 104268. doi:10.1016/j.jpet.2026.104268. Bloom NB, LaMalfa KS, Blough BE,
PAL-335
Chemical compound
As with other related substituted benzofuran derivatives such as 6-APB and 5-MAPB, 2-MAPB is a monoamine releaser with some selectivity for serotonin release
2-MAPB
Stimulant drug used as an appetite suppressant
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Amfepramone
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
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Clominorex
Pharmaceutical compound
(3T-MDMA; MY100) MY101 MY200 Indanes Amphetamines: 5-APDI (IAP) 5-MAPDI (IMP) Indoles Amphetamines: 5-API (5-IT; PAL-571) 6-API (6-IT) Naphthalenes Amphetamines:
MDM1EA
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
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
Entactogen
5-APB, also known as 5-(2-aminopropyl)benzofuran, is an entactogen of the phenethylamine, amphetamine, and benzofuran families. 5-APB and related drugs
5-APB
Central nervous system stimulant
amphetamine treatment for ADHD in children that found an average increase of 4.5 IQ points, continued increases in attention, and continued decreases in disruptive
Amphetamine
Group of stereoisomers
the serotonin 5-HT2A receptor and that they are mediated by induction of serotonin release as opposed to direct agonism of the serotonin 5-HT2A receptor
4-Hydroxyamphetamine
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
5-Trifluoromethyl-2-aminoindane (TAI) is a drug of the 2-aminoindane family with putative entactogenic effects. It acts as a serotonin releasing agent
Trifluoromethylaminoindane
Psychoactive research chemical
serotonin 5-HT2A receptor (Ki = 11,300 nM) and serotonin 5-HT2C receptor (Ki = 7,800 nM), similar to that of MDMA in the case of the serotonin 5-HT2A receptor
4-Fluoroamphetamine
Chemical compound
Compared to MDMA, EDMA was about half as potent as a serotonin releaser, 4.5-fold less potent as a norepinephrine releaser, and 8-fold less potent as a
EDMA
CNS stimulant and isomer of amphetamine
However, time to peak levels was delayed from 2.5 hours (range 1.5–6 hours) to 4.5 hours (range 2.5–8.0 hours). During oral selegiline therapy at a dosage
Levoamphetamine
Chemical compound
5-Chloro-αMT, also known as 5-chloro-α-methyltryptamine or as PAL-542, is a tryptamine derivative related to α-methyltryptamine (αMT) and one of only
5-Chloro-αMT
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
Protein-coding gene in the species Homo sapiens
paralyzing the normal function of the NET. At the same time, higher levels of 5-HT are maintained in the synapse increasing the concentrations of the latter
Norepinephrine_transporter
yl)-2β-(3'-phenylisoxazol-5'-yl)nortropane (FE-β-CPPIT) • N-(3'-Fluoropropyl-)-3β-(4'-chlorophenyl)-2β-(3'-phenylisoxazol-5'-yl)nortropane (FP-β-CPPIT) •
List_of_dopaminergic_drugs
Pharmaceutical compound
(3T-MDMA; MY100) MY101 MY200 Indanes Amphetamines: 5-APDI (IAP) 5-MAPDI (IMP) Indoles Amphetamines: 5-API (5-IT; PAL-571) 6-API (6-IT) Naphthalenes Amphetamines:
MYCO-002
Chemical compound
Piperazines: 2C-B-BZP BZP MBZP MDBZP MeOPP oMPP Others: 2-ADN 2-AI 2-AT 4-BP 5-APDI 5-IAI Amineptine Clofenciclan Cyclopentamine Cypenamine Cyprodenate Feprosidnine
Heptaminol
Mammalian protein found in Homo sapiens
monoamines and acetylcholine". Pflügers Archiv. 447 (5): 636–640. doi:10.1007/s00424-003-1100-5. PMID 12827358. S2CID 20764857. Tritsch NX, Ding JB, Sabatini
Vesicular monoamine transporter 2
Vesicular_monoamine_transporter_2
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5 APDI
5 APDI
5 APDI
5 APDI
5 APDI
5 APDI
5 APDI
5 APDI
5 APDI
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