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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8Cl2NO3S.Na
Molecular Weight 244.072
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AURICLOSENE MONOSODIUM

SMILES

[Na+].CC(C)(CS([O-])(=O)=O)N(Cl)Cl

InChI

InChIKey=NMHCZZRJHKDTBE-UHFFFAOYSA-M
InChI=1S/C4H9Cl2NO3S.Na/c1-4(2,7(5)6)3-11(8,9)10;/h3H2,1-2H3,(H,8,9,10);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H8Cl2NO3S
Molecular Weight 221.082
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Auriclosene (previously known as NVC-422) is a broad-spectrum, fast-acting topical anti-infective agent against microbial pathogens, including antibiotic-resistant microbes. It has been investigated in phase II clinical trials for the treatment of bacterial conjunctivitis and as a topical gel in children with impetigo. In addition, using a guinea pig model was shown, that auriclosene was effective in the treatment of dermatophytosis, including onychomycosis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Quaternary ammonium N,N-dichloroamines as topical, antimicrobial agents.
2009 May 15
Gallium(III) complexes with 2-acetylpyridine-derived thiosemicarbazones: antimicrobial and cytotoxic effects and investigation on the interactions with tubulin.
2013 Feb
Evaluation of antioxidant and antimicrobial activities of essential oils from Carum copticum seed and Ferula assafoetida latex.
2013 Feb
Broad-spectrum virucidal activity of (NVC-422) N,N-dichloro-2,2-dimethyltaurine against viral ocular pathogens in vitro.
2013 Feb 19
Patents

Sample Use Guides

Ophthalmic solution dispensed as drops onto the eye. Auriclosene Solution 0.3% | Dermal Gel applied 3 times per day for 7 days
Route of Administration: Other
NVC-422 (AURICLOSENE) reduced the viral titer of HAdV-5, HAdV-8, HAdV-19, HAdV-37, and HSV-1 by at least 4 logs after 1 hour incubation at 250 μM. Incubation of coxsackievirus A24 and enterovirus 70 with 2.5 mM NVC-422 for 1 hour reduced the viral titer by 4 logs and 4.5 logs, respectively. The virucidal activity of NVC-422 is maintained in the presence of 10% synthetic tears. In the EpiOcular corneal tissue model, NVC-422 was nonirritating at concentrations up to 41 mM.
Substance Class Chemical
Created
by admin
on Sat Dec 16 06:57:28 UTC 2023
Edited
by admin
on Sat Dec 16 06:57:28 UTC 2023
Record UNII
3L12631G2J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AURICLOSENE MONOSODIUM
Common Name English
AURICLOSENE MONOSODIUM ANHYDROUS
Common Name English
1-PROPANESULFONIC ACID, 2-(DICHLOROAMINO)-2-METHYL-, SODIUM SALT
Common Name English
1-PROPANESULFONIC ACID, 2-(DICHLOROAMINO)-2-METHYL-, SODIUM SALT (1:1)
Common Name English
Code System Code Type Description
CAS
1073913-47-9
Created by admin on Sat Dec 16 06:57:28 UTC 2023 , Edited by admin on Sat Dec 16 06:57:28 UTC 2023
PRIMARY
FDA UNII
3L12631G2J
Created by admin on Sat Dec 16 06:57:28 UTC 2023 , Edited by admin on Sat Dec 16 06:57:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID60148033
Created by admin on Sat Dec 16 06:57:28 UTC 2023 , Edited by admin on Sat Dec 16 06:57:28 UTC 2023
PRIMARY
PUBCHEM
25028238
Created by admin on Sat Dec 16 06:57:28 UTC 2023 , Edited by admin on Sat Dec 16 06:57:28 UTC 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY