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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17N3
Molecular Weight 215.2942
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRAMAZOLINE

SMILES

C1CN=C(NC2=C3CCCCC3=CC=C2)N1

InChI

InChIKey=QQJLHRRUATVHED-UHFFFAOYSA-N
InChI=1S/C13H17N3/c1-2-6-11-10(4-1)5-3-7-12(11)16-13-14-8-9-15-13/h3,5,7H,1-2,4,6,8-9H2,(H2,14,15,16)

HIDE SMILES / InChI

Molecular Formula C13H17N3
Molecular Weight 215.2942
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Tramazoline is a sympathomimetic drug that is used in the form of tramazoline hydrochloride in nasal decongestant preparations. Tramazoline is an α-adrenergic receptor agonist that inhibits secretion of nasal mucus.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
16.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Spray-Tish

Approved Use

Spray-Tish is a nasal decongestant. It works by clearing a stuffy or blocked nose by shrinking the inflamed and swollen blood vessels in the lining of the nose. Spray-Tish relieves a stuffy or blocked nose (nasal congestion) associated with the common cold, hayfever and rhinitis. A runny nose, nasal congestion, itching and sneezing, are typical symptoms of a condition known as rhinitis.
PubMed

PubMed

TitleDatePubMed
[The tolerability of nasal drugs with special regard to preservatives and physico-chemical parameters].
2003 Nov
Effects of topical mydriatics and vasoconstrictors on prostaglandin-E2-induced aqueous flare elevation in pigmented rabbits.
2003 Sep-Oct
The prevalence of allergic asthma and rhinitis in children of Polichni, Thessaloniki.
2004 Mar-Apr
The effect of nasal steroid administration on intraocular pressure.
2007 Jul
Tramazoline turns asymptomatic into symptomatic hyper-CK-emia.
2007 Mar
Patents

Sample Use Guides

The recommended dose for adults and children six years of age and over is 1 to 2 sprays into each nostril up to four times daily as required.
Route of Administration: Nasal
In Vitro Use Guide
Binding affinity of Tramazoline against Alpha-2 adrenergic receptor measured as the ability to inhibit the specific [3H]clonidine binding (0.4 nM) to rat isolated brain membranes by 50% was 16 nM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:14:24 UTC 2023
Edited
by admin
on Fri Dec 15 15:14:24 UTC 2023
Record UNII
SLE31693IV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRAMAZOLINE
INN   MI   WHO-DD  
INN  
Official Name English
TRAMAZOLINE [MI]
Common Name English
2-((5,6,7,8-TETRAHYDRO-1-NAPHTHYL)AMINO)-2-IMIDAZOLINE
Systematic Name English
Tramazoline [WHO-DD]
Common Name English
MUCONASAL
Brand Name English
tramazoline [INN]
Common Name English
1H-IMIDAZOL-2-AMINE, 4,5-DIHYDRO-N-(5,6,7,8-TETRAHYDRO-1-NAPHTHALENYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
WHO-VATC QR01AA09
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
WHO-ATC R01AA09
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
Code System Code Type Description
RXCUI
38453
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID5046936
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
DRUG CENTRAL
3620
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
SMS_ID
100000077217
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
PUBCHEM
5524
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
DRUG BANK
DB13064
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
MERCK INDEX
m10997
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C87582
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
ChEMBL
CHEMBL32573
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
CAS
1082-57-1
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
EVMPD
SUB11211MIG
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
INN
1831
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
ECHA (EC/EINECS)
214-105-6
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
MESH
C005370
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
WIKIPEDIA
TRAMAZOLINE
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
FDA UNII
SLE31693IV
Created by admin on Fri Dec 15 15:14:24 UTC 2023 , Edited by admin on Fri Dec 15 15:14:24 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY