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Details

Stereochemistry RACEMIC
Molecular Formula C7H17N.ClH
Molecular Weight 151.678
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TUAMINOHEPTANE HYDROCHLORIDE

SMILES

Cl.CCCCCC(C)N

InChI

InChIKey=JOPQZCZKKFHRNT-UHFFFAOYSA-N
InChI=1S/C7H17N.ClH/c1-3-4-5-6-7(2)8;/h7H,3-6,8H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H17N
Molecular Weight 115.2166
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Tuaminoheptane (or 2-aminoheptane), a nasal decongestant that is on the list of prohibited substances published by the World Anti-Doping Agency due to its stimulating properties. Tuaminoheptane is a stimulant of the sympathetic nervous system, similarly to several other known drugs targeting norepinephrine transporter

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Determination of tuaminoheptane in doping control urine samples.
2007
Patents

Sample Use Guides

Unknown
Route of Administration: Nasal
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:00:02 GMT 2023
Edited
by admin
on Sat Dec 16 10:00:02 GMT 2023
Record UNII
052153358W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TUAMINOHEPTANE HYDROCHLORIDE
MI  
Common Name English
2-HEPTANAMINE, HYDROCHLORIDE (1:1)
Systematic Name English
TUAMINOHEPTANE HYDROCHLORIDE [MI]
Common Name English
TUAMINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
MERCK INDEX
m11252
Created by admin on Sat Dec 16 10:00:02 GMT 2023 , Edited by admin on Sat Dec 16 10:00:02 GMT 2023
PRIMARY Merck Index
CAS
6159-35-9
Created by admin on Sat Dec 16 10:00:02 GMT 2023 , Edited by admin on Sat Dec 16 10:00:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID70977179
Created by admin on Sat Dec 16 10:00:02 GMT 2023 , Edited by admin on Sat Dec 16 10:00:02 GMT 2023
PRIMARY
FDA UNII
052153358W
Created by admin on Sat Dec 16 10:00:02 GMT 2023 , Edited by admin on Sat Dec 16 10:00:02 GMT 2023
PRIMARY
PUBCHEM
18686558
Created by admin on Sat Dec 16 10:00:02 GMT 2023 , Edited by admin on Sat Dec 16 10:00:02 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY