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주요 문서

COO/COA

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M3404

(±)-p-Methoxyamphetamine hydrochloride

Name: (±)-<I>p</I>-Methoxyamphetamine hydrochloride
Brand: SIGMA

동의어(들):

PMA hydrochloride

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모든 사진(1)

About This Item

실험식(Hill 표기법):

C₁₀H₁₅NO · HCl

CAS Number:

52740-56-4

Molecular Weight:

201.69

MDL number:

MFCD00051431

UNSPSC 코드:

12352200

PubChem Substance ID:

24896840

가격 및 재고 정보를 현재 이용할 수 없음

약물 제어

USDEA Schedule I; Home Office Schedule 1; stupéfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

forensics and toxicology
veterinary

SMILES string

Cl.COc1ccc(CC(C)N)cc1

유사한 제품을 찾으십니까? 방문 제품 비교 안내

생화학적/생리학적 작용

CNS stimulant and hallucinogen; more potent transport inhibitor and releaser of serotonin than of dopamine.

픽토그램

GHS06

신호어

Danger

유해 및 위험 성명서

H301

예방조치 성명서

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

4-Ethoxyamphetamine: effects on intracranial self-stimulation and in vitro uptake and release of 3H-dopamine and 3H-serotonin in the brains of rats.

K M Hegadoren et al.

Journal of psychiatry & neuroscience : JPN, 19(1), 57-62 (1994-01-01)

Experiments were conducted to compare the effects of 4-ethoxyamphetamine, a novel "designer" amphetamine, with (+)-amphetamine and an earlier "designer" amphetamine, 4-methoxyamphetamine, on rats. (+)-Amphetamine significantly decreased frequency threshold measures in an intracranial self-stimulation (ICSS) procedure using medial forebrain bundle electrodes

Interactions of amphetamine analogs with human liver CYP2D6.

D Wu et al.

Biochemical pharmacology, 53(11), 1605-1612 (1997-06-01)

The interaction of fifteen amphetamine analogs with the genetically polymorphic enzyme CYP2D6 was examined. All fourteen phenylisopropylamines tested were competitive inhibitors of CYP2D6 in human liver microsomes. The presence of a methylenedioxy group in the 3,4-positions of both amphetamine (Ki

In vivo analysis of serotonin clearance in rat hippocampus reveals that repeated administration of p-methoxyamphetamine (PMA), but not 3,4-methylenedioxymethamphetamine (MDMA), leads to long-lasting deficits in serotonin transporter function.

Paul D Callaghan et al.

Journal of neurochemistry, 100(3), 617-627 (2006-12-22)

p-Methoxyamphetamine (PMA) has been implicated in fatalities as a result of 'ecstasy' (MDMA) overdose worldwide. Like MDMA, acute effects are associated with marked changes in serotonergic neurotransmission, but the long-term effects of PMA are poorly understood. The aim of this

Trafficking properties and activity regulation of the neuronal glycine transporter GLYT2 by protein kinase C.

Amparo Fornés et al.

The Biochemical journal, 412(3), 495-506 (2008-03-18)

The neuronal glycine transporter GLYT2 controls the availability of the neurotransmitter in glycinergic synapses, and the modulation of its function may influence synaptic transmission. The active transporter is located in membrane rafts and reaches the cell surface through intracellular trafficking.

Fatal paramethoxy-amphetamine (PMA) poisoning in the Australian Capital Territory.

Paul G Lamberth et al.

The Medical journal of Australia, 188(7), 426-426 (2008-04-09)

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