4-METHYLAMPHETAMINE

Details

Stereochemistry	RACEMIC
Molecular Formula	C10H15N
Molecular Weight	149.2328
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CC(N)CC1=CC=C(C)C=C1

InChI

InChIKey=ZDHZDWSHLNBTEB-UHFFFAOYSA-N

InChI=1S/C10H15N/c1-8-3-5-10(6-4-8)7-9(2)11/h3-6,9H,7,11H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C10H15N
Molecular Weight	149.2328
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Overview

CYP3A4	CYP2C9	CYP2D6	hERG
substrate 1,737	substrate 1,037	substrate 1,217

OverviewOther

Other Inhibitor	Other Substrate	Other Inducer
	CYP1A2 1,054 CYP2A6 543 CYP2B6 664 CYP2C8 693 CYP2C19 991 CYP2E1 667 CYP3A5 395

Drug as victim

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Target	Modality	Activity
CYP1A2 1,054	substrate 3,367	no
CYP2A6 543	substrate 3,367	no
CYP2B6 664	substrate 3,367	no
CYP2C19 991	substrate 3,367	no
CYP2C8 693	substrate 3,367	no

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Sourcing

Sourcing

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Vendor/Aggregator	ID	URL
1PlusChem LLC	1P00D7AD
ABI Chem	AC1L56QA
Alichem	490022903	http://www.alichem.com/en/products/64-11-9.html
AstaTech	N10874
AstaTech	N14354

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Patents

Patents

Substance Class	Chemical
Record UNII	9E273KL7HS
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

4-METHYLAMPHETAMINE

Systematic Name

English

PAL-313

Code

English

1-(4-METHYLPHENYL)PROPAN-2-AMINE

Systematic Name

English

APTROL

Brand Name

English

P-METHYLAMFETAMINE

Common Name

English

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Classification Tree

Code System

Code

Empathogens

WIKIPEDIA

Designer-drugs-4-MA

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Code System

Code

Type

Description

FDA UNII

9E273KL7HS

PRIMARY

EPA CompTox

DTXSID50945351

PRIMARY

WIKIPEDIA

4-METHYLAMPHETAMINE

PRIMARY

4-Methylamphetamine (4-MA; PAL-313; Aptrol; p-TAP) is a stimulant and anorectic drug of the phenethylamine and amphetamine chemical classes.In vitro, it acts as a potent and balanced serotonin, norepinephrine, and dopamine releasing agent with Ki affinity values of 53.4nM, 22.2nM, and 44.1nM at the serotonin, norepinephrine, and dopamine transporters, respectively.

CAS

22683-78-9

SUPERSEDED

PUBCHEM

199116

PRIMARY

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Related Record

Type

Details