| 词条 | Β-Methylphenethylamine |
| 释义 |
| verifiedrevid = 449584722 | IUPAC_name = 2-Phenylpropan-1-amine | image = Beta-methylphenethylamine.png | image2 = Beta-Methylphenethylamine molecule ball.png | drug_name = β-Methylphenethylamine | tradename = | pregnancy_category = | legal_status = Uncontrolled | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|PubChem}} | CAS_number = 582-22-9 | ATC_prefix = none | ATC_suffix = | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 6XL7O3V13L | ChEMBL = 158578 | PubChem = 11398 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 10920 | C=9 | H=13 | N=1 | smiles = NCC(c1ccccc1)C | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C9H13N/c1-8(7-10)9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = AXORVIZLPOGIRG-UHFFFAOYSA-N | density = 0.93 | boiling_point = 80 | boiling_notes = (at 10 mm Hg) }} β-Methylphenethylamine (β-Me-PEA, BMPEA, or 1-amino-2-phenylpropane) is an organic compound of the phenethylamine class, and a positional isomer of the drug amphetamine, with which it shares some properties. In particular, both amphetamine and β-methylphenethylamine are human TAAR1 agonists.[1] In appearance, it is a colorless or yellowish liquid. Relatively little information has been published about this substance. Hartung and Munch reported that it had good antihypotensive (pressor) activity in experimental animals, and that it was orally active. The MLD (minimum lethal dose) for the HCl salt was given as 500 mg/kg (rat, s.c.) and 50 mg/kg (rabbit, i.v.).[2] A study by Graham and co-workers at the Upjohn Co., comparing a large number of β-methylphenethylamines substituted on the benzene ring showed that β-methylphenethylamine itself had 1/700 x the pressor activity of epinephrine, corresponding to ~ 1/3 the potency of amphetamine. The β-methyl compound also had ~ 2 x the broncho-dilating power of amphetamine (as measured using the isolated rabbit lung), and an LD50 of 50 mg/kg (rat, i.v.).[3] Synthesisβ-Methylphenethylamine can be made by the catalytic hydrogenation of 2-phenylpropionitrile with Pd/C in pure anhydrous ethanol containing 3 equivalents of HCl; the finished product is extracted as the HCl salt, m.p. 123-124°.[2] PresenceIn 2015, 52% of supplements labeled as containing Acacia rigidula were found to contain BMPEA.[4][5] Consumers following recommended maximum daily servings would consume a maximum of 94 mg of BMPEA per day.[4] In 2012, however, the FDA determined that BMPEA was not naturally present in Acacia rigidula leaves.[6] This question was litigated during the trial of Hi Tech Pharmaceuticals Inc vs. Cohen.[7][8] Despite US Food and Drug Administration warning letters, BMPEA remains present in dietary supplements.[9] Safetyβ-Methylphenethylamine was associated with a case of cerebral hemorrhage in a Swedish athlete and first time user. The female victim with no medical history had taken a Swedish food supplement with 290 mg β-methylphenethylamine per serving before commencing her usual exercises. After about 30 minutes the first symptoms appeared. The presence of the active ingredient was not declared on the label.[10] Use of β-Methylphenethylamine is also prohibited in sport.[11] See also
References1. ^{{ cite journal | vauthors = Wainscott DB, Little SP, Yin T, Tu Y, Rocco VP, He JX, Nelson DL | title = Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1 | journal = The Journal of Pharmacology and Experimental Therapeutics | year = 2007 | volume = 320 | issue = 1 | pages = 475–85 | pmid = 17038507 | doi = 10.1124/jpet.106.112532 | quote = The effect of β-carbon substitution on the phenylethylamine side chain was also investigated (Table 3). A β-methyl substituent was well tolerated compared with β-PEA. In fact, S-(–)-β-methyl-β-PEA was as potent as β-PEA at human TAAR1. }} {{Monoamine releasing agents}}{{TAAR ligands}}{{Phenethylamines}}{{DEFAULTSORT:Methylphenethylamine, Beta-}}2. ^1 {{ cite journal | vauthors = Hartung WH, Munch JC | title = Amino alcohols. VI. The preparation and pharmacodynamic activity of four isomeric phenylpropylamines | journal = J. Am. Chem. Soc. | year = 1931 | volume = 53 | issue = 5 | pages = 1875–9 | doi = 10.1021/ja01356a036 }} 3. ^{{ cite journal | vauthors = Graham BE, Cartland GF, Woodruff EH | title = Phenyl propyl and phenyl isopropyl amines. Changes in pharmacological action on substitution of phenyl nucleus and amino nitrogen | journal = Ind. Eng. Chem. | year = 1945 | volume = 37 | issue = 2 | pages = 149–51 | doi = 10.1021/ie50422a010 }} 4. ^1 {{cite journal | title = An amphetamine isomer whose efficacy and safety in humans has never been studied, β-methylphenylethylamine (BMPEA), is found in multiple dietary supplements – Cohen – 2015 – Drug Testing and Analysis – Wiley Online Library | doi=10.1002/dta.1793 | pmid=25847603 | volume=8 | issue=3–4 | journal=Drug Testing and Analysis | pages=328–333|year = 2016|last1 = Cohen|first1 = Pieter A.| last2=Bloszies | first2=Clayton | last3=Yee | first3=Caleb | last4=Gerona | first4=Roy }} 5. ^{{cite news |agency= |title=Conflicts of Interest at the F.D.A. |url=https://www.nytimes.com/2015/04/13/opinion/conflicts-of-interest-at-the-fda.html |quote= they identified BMPEA in 11 of 21 brands of supplements with acacia rigidula listed as an ingredient.|newspaper=New York Times |date=April 13, 2015 |accessdate=2015-04-13 }} 6. ^{{cite web|url=http://www.webmd.com/vitamins-and-supplements/news/20150407/bmpea-acacia-rigidula-supplments|title=Untested Stimulant Still in Dietary Supplements|author=Brenda Goodman|publisher=WebMD|date=7 April 2015}} 7. ^{{cite news |title=How a supplement maker tried to silence a Harvard doctor |url=https://www.statnews.com/2017/01/10/supplement-harvard-pieter-cohen/ |work=STAT |date=10 January 2017}} 8. ^{{cite journal |last1=Bagley |first1=Nicolas |last2=Carroll |first2=Aaron E. |last3=Cohen |first3=Pieter A. |title=Scientific Trials—In the Laboratories, Not the Courts |journal=JAMA Internal Medicine |date=1 January 2018 |volume=178 |issue=1 |pages=7 |doi=10.1001/jamainternmed.2017.5730}} 9. ^{{cite journal |last1=Cohen |first1=Pieter A. |last2=Wen |first2=Anita |last3=Gerona |first3=Roy |title=Prohibited Stimulants in Dietary Supplements After Enforcement Action by the US Food and Drug Administration |journal=JAMA Internal Medicine |date=1 December 2018 |volume=178 |issue=12 |pages=1721 |doi=10.1001/jamainternmed.2018.4846}} 10. ^{{ cite journal | vauthors = Cohen PA, Zeijlon R, Nardin R, Keizers PH, Venhuis BJ | title = Hemorrhagic Stroke Probably Caused by Exercise Combined With a Sports Supplement Containing β-Methylphenyl-ethylamine (BMPEA): A Case Report | journal = Ann. Intern. Med. | year = 2015 | volume = 162 | issue = 16 | pages = 879–80 | doi = 10.7326/L15-5101 | pmid=26075771}} 11. ^{{ cite journal | vauthors = Cholbiński P, Wicka M, Kowalczyk K, Jarek A, Kaliszewski P, Pokrywka A, Bulska E, Kwiatkowska D | title = Detection of β-methylphenethylamine, a novel doping substance, by means of UPLC/MS/MS | journal = Anal Bioanal Chem | year = 2014 | volume = 406 | issue = 15 | pages = 3681–8 | doi = 10.1007/s00216-014-7728-5 | pmid = 24633566 | pmc = 4026626 }} 4 : Stimulants|Phenethylamines|TAAR1 agonists|Norepinephrine releasing agents |
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