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Details

Stereochemistry RACEMIC
Molecular Formula C10H11N3O5S
Molecular Weight 285.276
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NIFURATEL

SMILES

CSCC1CN(\N=C\C2=CC=C(O2)[N+]([O-])=O)C(=O)O1

InChI

InChIKey=SRQKTCXJCCHINN-NYYWCZLTSA-N
InChI=1S/C10H11N3O5S/c1-19-6-8-5-12(10(14)18-8)11-4-7-2-3-9(17-7)13(15)16/h2-4,8H,5-6H2,1H3/b11-4+

HIDE SMILES / InChI
Nifuratel is a furane-derivative provided with a strong trichomonicidal activity; it has a broad antibacterial spectrum of action, including both Gram-negative and Gram-positive organisms. It is active against Chlamydia trachomatis and Mycoplasma spp. and has also some degree of activity against Candida spp. and mycetes. The action mechanism of nitrofurans has not been fully elucidated, and it may be the inhibiting of acetyl coenzyme A interfere with the early stages of bacterial glucose metabolism. Nifuratel alone or in complex with nystatin is indicated for the treatment of vulvovaginal and urinary tract infections. The drug is not approved by FDA.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
MACMIROR

Approved Use

MACMIROR (nifuratel ) is indicated for the treatment of vulvovaginal infections and vaginal discharge caused by pathogenic microorganisms: Trichomonas, Monilia, micelles. Urinary tract infections.
Curative
MACMIROR

Approved Use

MACMIROR (nifuratel ) is indicated for the treatment of vulvovaginal infections and vaginal discharge caused by pathogenic microorganisms: Trichomonas, Monilia, micelles. Urinary tract infections.
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

MACMIROR tablets (200 mg nifuratel) for the treatment of vaginal infections: 1 tablet 3 times daily after meals for 1 week, for both partners. Urinary tract infections: 3 to 6 tablets per day for 1-2 weeks, depending on the cause and severity of the infection. MACMIROR complex vaginal capsules (500 mg nifuratel / 200 000 nystatin): 1 vaginal capsule daily or as directed by your doctor.
Route of Administration: Other
In vitro, nifuratel is able to inhibit the growth of A. vaginae, with a MIC range of 0.125-1 μg/mL; it is active against G. vaginalis (MICs ranging from <0.125 to 4 μg/ml) and does not affect lactobacilli.
Name Type Language
NIFURATEL
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
5-(METHYLTHIOMETHYL)-3-(5-NITRO-2-FURFURYLIDENAMINO)OXAZOLIDIN-2-ONE
Common Name English
NF-113
Code English
NIFURATEL [MART.]
Common Name English
Nifuratel [WHO-DD]
Common Name English
SAP-113
Code English
2-OXAZOLIDINONE, 5-((METHYLTHIO)METHYL)-3-(((5-NITRO-2-FURANYL)METHYLENE)AMINO)-
Systematic Name English
5-((METHYLTHIO)METHYL)-3-(((5-NITRO-2-FURANYL)METHYLENE)AMINO)-2-OXAZOLIDINONE
Systematic Name English
NIFURATEL [USAN]
Common Name English
OMNES
Brand Name English
METHYLMERCADONE
Common Name English
INIMUR
Brand Name English
5-[(Methylthio)methyl]-3-[(5-nitrofurfurylidene)amino]-2-oxazolidinone
Systematic Name English
TYDANTIL
Common Name English
NIFURATEL [MI]
Common Name English
nifuratel [INN]
Common Name English
MAGMILOR
Brand Name English
POLMIROR
Brand Name English
5-(METHYLMERCAPTOMETHYL)-3-(5-NITRO-2-FURFURYLIDENAMINO)-2-OXAZOLIDINONE
Common Name English
MACMIROR
Brand Name English
3-((5-NITRO-2-FURFURYLIDENE)AMINO)-5-((METHYLTHIO)METHYL)-2-OXAZOLIDINONE
Common Name English
2-OXAZOLIDINONE, 5-((METHYLTHIO)METHYL)-3-((5-NITROFURFURYLIDENE)AMINO)-
Systematic Name English
Classification Tree Code System Code
WHO-ATC G01AX05
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
WHO-VATC QG01AX05
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
Code System Code Type Description
INN
2314
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
MESH
D009545
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL514315
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
FDA UNII
U60U6P08SP
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
DRUG CENTRAL
1926
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
MERCK INDEX
m7886
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY Merck Index
RXCUI
7419
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY RxNorm
SMS_ID
100000090771
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
PUBCHEM
6433427
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
WIKIPEDIA
NIFURATEL
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID60863471
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
EVMPD
SUB09261MIG
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
225-576-2
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
CAS
4936-47-4
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
DRUG BANK
DB13724
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY
NCI_THESAURUS
C170220
Created by admin on Sat Dec 16 17:13:21 GMT 2023 , Edited by admin on Sat Dec 16 17:13:21 GMT 2023
PRIMARY