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・ 1-acylglycerophosphocholine O-acyltransferase
・ 1-alkenyl-2-acylglycerol choline phosphotransferase
・ 1-alkenylglycerophosphocholine O-acyltransferase
・ 1-alkenylglycerophosphoethanolamine O-acyltransferase
・ 1-alkyl-2-acetylglycerol O-acyltransferase
・ 1-alkyl-2-acetylglycerophosphocholine esterase
・ 1-alkylglycerophosphocholine O-acetyltransferase
・ 1-alkylglycerophosphocholine O-acyltransferase
・ 1-alpha-O-Galloylpunicalagin
・ 1-Amino-2-propanol
・ 1-Amino-2-propanone
・ 1-Amino-3-phenylindole
・ 1-aminocyclopropane-1-carboxylate deaminase
・ 1,3-Benzodioxolyl-N-methylbutanamine
・ 1,3-Benzodioxolyl-N-methylpentanamine
1,3-Benzodioxolylbutanamine
・ 1,3-beta-D-glucan phosphorylase
・ 1,3-beta-galactosyl-N-acetylhexosamine phosphorylase
・ 1,3-Beta-glucan synthase
・ 1,3-beta-oligoglucan phosphorylase
・ 1,3-Bis(dicyanomethylene)squarate
・ 1,3-Bis(diphenylphosphino)propane
・ 1,3-Bisphosphoglyceric acid
・ 1,3-Butadiene
・ 1,3-Butadiene (data page)
・ 1,3-Butanediol
・ 1,3-Cycloheptadiene
・ 1,3-Cyclohexadiene
・ 1,3-DCP
・ 1,3-Dehydroadamantane


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1,3-Benzodioxolylbutanamine : ウィキペディア英語版
1,3-Benzodioxolylbutanamine

1,3-Benzodioxolylbutanamine, 3,4-Methylenedioxybutanphenamine, MDB, (BDB; J; 3,4-methylenedioxy-α-ethylphenethylamine) is an entactogenic drug of the phenethylamine chemical class.〔Bronson ME, Jiang W, DeRuiter J, Clark CR. A behavioral comparison of Nexus, cathinone, BDB, and MDA. Pharmacology, Biochemistry and Behaviour. 1995 Jun-Jul;51(2-3):473-5.〕 It is the α-ethyl analogue of methylenedioxyphenethylamine (MDPEA) and MDA.
BDB was first synthesized by Alexander Shulgin. In his book ''PiHKAL (Phenethylamines i Have Known And Loved)'', the dosage range is listed as 150–230 mg, and the duration is listed as 4–8 hours. BDB produces entactogenic, MDMA-like effects. While pleasant and euphoric, BDB is also fairly sedating and some users feel that the lack of stimulant effect makes it less enjoyable than other similar drugs. Additional side effects associated with BDB include nystagmus and dizziness. Very little data exists about the pharmacological properties, metabolism, and toxicity of BDB.
Animal studies and anecdotal reports show that BDB is a slightly more potent serotonin releasing agent than its methylated sister compound methylbenzodioxylbutanamine (MBDB; "Eden", "Methyl-J").〔Bronson ME, Jiang W, DeRuiter J, Clark CR. Structure-activity relationships of BDB and its monomethyl and dimethyl derivatives. Pharmacology, Biochemistry and Behaviour. 1995 Jun-Jul;51(2-3):477-9.〕 However, it is more commonly known as a metabolite of the ''N''-alkylated analogues MBDB and ethylbenzodioxylbutanamine (EBDB; "Ethyl-J") which have appeared in so-called methylenedioxymethamphetamine (MDMA; "Ecstasy", "Adam", "Empathy", "Molly", "E", "X", "XTC") tablets.〔Kintz P. Excretion of MBDB and BDB in urine, saliva, and sweat following single oral administration. Journal of Analytical Toxicology. 1997 Nov-Dec;21(7):570-5.〕〔Garofano L, Santoro M, Patri P, Guidugli F, Bollani T, Favretto D, Traldi P. Ion trap mass spectrometry for the characterization of N-methyl-1- (3,4-methylene-dioxyphenyl)-2-butanamine and N-ethyl-3,4- methylenedioxyamphetamine, two widely distributed street drugs. Rapid Communications in Mass Spectrometry. 1998;12(12):779-82.〕 While BDB itself has not been reported as being sold as "Ecstasy", urine analysis of "Ecstasy" users suggest that this drug may have appeared as a street drug, although it is unclear whether the positive urine test for BDB resulted from consumption of BDB itself or merely as a metabolite of MBDB.〔Kronstrand R. Identification of N-methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine (MBDB) in urine from drug users. Journal of Analytical Toxicology. 1996 Oct;20(6):512-6.〕
==See also==

* α-Ethylphenethylamine
* 1-(4-Methylphenyl)-2-aminobutane
* Ethylbenzodioxolylbutanamine (EBDB; Ethyl-J)
* Methylbenzodioxolylbutanamine (MBDB; Methyl-J; "Eden")

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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