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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

Description

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

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
MACMIROR
Curative
MACMIROR

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
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 Use Guide
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.