CAMFETAMINE

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NCATS

Details

Stereochemistry	MIXED
Molecular Formula	C14H19N
Molecular Weight	201.3074
Optical Activity	UNSPECIFIED
Defined Stereocenters	0 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CAMFETAMINE

Structure Search

SMILES

CNC1C2CCC(C2)C1C3=CC=CC=C3

InChI

InChIKey=CTVMYAZECFXZLN-UHFFFAOYSA-N

InChI=1S/C14H19N/c1-15-14-12-8-7-11(9-12)13(14)10-5-3-2-4-6-10/h2-6,11-15H,7-9H2,1H3

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary Target	Pharmacology	Condition	Potency
Cytochrome P450 2B6 19 Target ID: CHEMBL4729 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25136586 \| https://www.ncbi.nlm.nih.gov/pubmed/24828975	Substrate 661
Cytochrome P450 2C19 51 Target ID: CHEMBL3622 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25136586 \| https://www.ncbi.nlm.nih.gov/pubmed/24828975	Substrate 661
Cytochrome P450 2D6 61 Target ID: CHEMBL289 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25136586 \| https://www.ncbi.nlm.nih.gov/pubmed/24828975	Substrate 661
Cytochrome P450 3A4 127 Target ID: CHEMBL340 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25136586 \| https://www.ncbi.nlm.nih.gov/pubmed/24828975	Substrate 661
Cytochrome P450 1A2 72 Target ID: CHEMBL3356 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25136586 \| https://www.ncbi.nlm.nih.gov/pubmed/24828975	Substrate 661

Name

Type

Language

CAMFETAMINE

Common Name

English

BICYCLO(2.2.1)HEPTAN-2-AMINE, N-METHYL-3-PHENYL-

Systematic Name

English

2-NORBORNANAMINE, N-METHYL-3-PHENYL-

Systematic Name

English

N-METHYL-3-PHENYLBICYCLO(2.2.1)HEPTAN-2-AMINE

Systematic Name

English

Classification Tree Code System Code

WIKIPEDIA

Designer-drugs-Camfetamine

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

Code System Code Type Description

PUBCHEM

57504017

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

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FDA UNII

3E7N2GO76U

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

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EPA CompTox

DTXSID40101719

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

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WIKIPEDIA

Camfetamine

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

PRIMARY

Camfetamine (N-methyl-3-phenyl-norbornan-2-amine) is a stimulant drug closely related to the appetite suppressant fencamfamine, being its N-methyl homologue. It has been sold as a designer drug following the banning of mephedrone and related substituted cathinone derivatives in many countries, and reportedly has slightly stronger stimulant effects than fencamfamine, but with correspondingly more severe side effects.

MANUFACTURER PRODUCT INFORMATION

N-METHYL-3-PHENYLBICYCLO(2.2.1)HEPTAN-2-AMINE

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

PRIMARY

Camfetamine is the N-methyl analogue of norFencamfamine, producing it's effects primarily as a dopamine reuptake inhibitor, appearing on the RC scene in 2011. Dosage: Effects and contraindications are likely to be similar to similar to fencafamine: Light: 50-100mg; common 100-150mg; heavy: 200-250mg+

CAS

92499-19-9

Created by admin on Sat Dec 16 10:36:47 GMT 2023 , Edited by admin on Sat Dec 16 10:36:47 GMT 2023

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ACTIVE MOIETY


					3E7N2GO76U

PARENT (SALT/SOLVATE)


					29EPO56C7W

CAMFETAMINE HYDROCHLORIDE