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Details

Stereochemistry ACHIRAL
Molecular Formula C32H55N4O
Molecular Weight 511.8053
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of THONZONIUM

SMILES

CCCCCCCCCCCCCCCC[N+](C)(C)CCN(CC1=CC=C(OC)C=C1)C2=NC=CC=N2

InChI

InChIKey=IOYZYMQFUSNATM-UHFFFAOYSA-N
InChI=1S/C32H55N4O/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-27-36(2,3)28-26-35(32-33-24-19-25-34-32)29-30-20-22-31(37-4)23-21-30/h19-25H,5-18,26-29H2,1-4H3/q+1

HIDE SMILES / InChI
Thonzonium Bromide is a cationic surface-active compound. As an additive to pharmacologic formulations, thonzonium bromide causes dispersion and penetration of cellular debris and exudate, thereby promoting tissue contact of the administered medication. Thonzonium bromide is a component of FDA-approved Coly-Mycin S Otic, used for treating infections of the ear caused by certain bacteria. It has being shown that Thonzonium bromide inhibits RANKL-induced osteoclast formation and bone resorption in vitro and prevents LPS-induced bone loss in vivo, suggesting that Thonzonium bromide might be a useful alternative therapy in preventing or treating osteolytic diseases..

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
COLY-MYCIN S

Approved Use

Cortisporin®-TC Otic Suspension is indicated for the treatment of superficial bacterial infections of the external auditory canal, caused by organisms susceptible to the action of the antibiotics; and for the treatment of infections of mastoidectomy and fenestration cavities, caused by organisms susceptible to the antibiotics.

Launch Date

-2.40710402E11
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Thermal decomposition of thonzonium bromide.
1986 Oct
Inhibitors of V-ATPase proton transport reveal uncoupling functions of tether linking cytosolic and membrane domains of V0 subunit a (Vph1p).
2012 Mar 23
Thonzonium bromide inhibits RANKL-induced osteoclast formation and bone resorption in vitro and prevents LPS-induced bone loss in vivo.
2016 Mar 15
Patents

Sample Use Guides

Mice: 5 mg/kg body weight, subcutaneous injection
Route of Administration: Other
Mature osteoclasts (OCs) exposed to Thonzonium (100 or 200 nM) for 48 h demonstrated attenuated capacity to resorb bone (reduction of 30% and 80% respectively).
Name Type Language
THONZONIUM
Common Name English
Tonzonium [WHO-DD]
Common Name English
N-(2-((4-METHOXYBENZYL)(PYRIMIDIN-2-YL)AMINO)ETHYL)-N,N-DIMETHYLHEXADECAN-1-AMINIUM
Systematic Name English
TONZONIUM
WHO-DD  
Common Name English
THONZONIUM ION
Common Name English
THONZONIUM CATION
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID8048232
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
DAILYMED
Z05ZE98FV8
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
RXCUI
237058
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY RxNorm
PUBCHEM
5456
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
DRUG BANK
DB09552
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
DRUG CENTRAL
4605
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
CAS
25466-36-8
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
FDA UNII
Z05ZE98FV8
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY
WIKIPEDIA
Thonzonium
Created by admin on Fri Dec 15 15:47:42 UTC 2023 , Edited by admin on Fri Dec 15 15:47:42 UTC 2023
PRIMARY