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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17N3.ClH.H2O
Molecular Weight 269.77
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRAMAZOLINE HYDROCHLORIDE MONOHYDRATE

SMILES

O.Cl.C1CN=C(NC2=C3CCCCC3=CC=C2)N1

InChI

InChIKey=FDPYEAXJRLQOGE-UHFFFAOYSA-N
InChI=1S/C13H17N3.ClH.H2O/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);1H;1H2

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

Molecular Formula H2O
Molecular Weight 18.0153
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 prevalence of allergic asthma and rhinitis in children of Polichni, Thessaloniki.
2004 Mar-Apr
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 18:46:01 GMT 2023
Edited
by admin
on Fri Dec 15 18:46:01 GMT 2023
Record UNII
9DF5N42U1U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRAMAZOLINE HYDROCHLORIDE MONOHYDRATE
EP  
Common Name English
1H-IMIDAZOL-2-AMINE, 4,5-DIHYDRO-N-(5,6,7,8-TETRAHYDRO-1-NAPHTHALENYL)-, MONOHYDROCHLORIDE, MONOHYDRATE
Common Name English
TRAMAZOLINE HYDROCHLORIDE MONOHYDRATE [EP MONOGRAPH]
Common Name English
N-(5,6,7,8-TETRAHYDRONAPHTHALEN-1-YL)-4,5-DIHYDRO-1H-IMIDAZOL-2-AMINE HYDROCHLORIDE MONOHYDRATE
Systematic Name English
Code System Code Type Description
CAS
74195-73-6
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
PUBCHEM
19379147
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
EVMPD
SUB20996
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID30225188
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
FDA UNII
9DF5N42U1U
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
SMS_ID
100000087292
Created by admin on Fri Dec 15 18:46:01 GMT 2023 , Edited by admin on Fri Dec 15 18:46:01 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY