Details
Stereochemistry | RACEMIC |
Molecular Formula | C18H15Cl3N2S.HNO3 |
Molecular Weight | 460.762 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O[N+]([O-])=O.ClC1=CC=C(CSC(CN2C=CN=C2)C3=C(Cl)C=C(Cl)C=C3)C=C1
InChI
InChIKey=CRKGMGQUHDNAPB-UHFFFAOYSA-N
InChI=1S/C18H15Cl3N2S.HNO3/c19-14-3-1-13(2-4-14)11-24-18(10-23-8-7-22-12-23)16-6-5-15(20)9-17(16)21;2-1(3)4/h1-9,12,18H,10-11H2;(H,2,3,4)
Molecular Formula | C18H15Cl3N2S |
Molecular Weight | 397.749 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | HNO3 |
Molecular Weight | 63.0128 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.drugs.com/cdi/sulconazole-cream.html
Sources: https://www.drugs.com/cdi/sulconazole-cream.html
Sulconazole (trade name Exelderm) is an antifungal medication of the imidazole class. Sulconazole has a broad spectrum of antifungal activity in vitro and has been shown to be an effective topical antifungal agent for the management of superficial fungal infections of the skin, particularly dermatophytosis and tinea versicolor. Sulconazole inhibits the cytochrome P-450 isoenzyme, C-14-alpha-demethylase by binding to the heme iron of the enzyme. This results in a largely fungistatic effect. The selectivity of azole antifungal agents for pathogenic organisms compared with mammalian cells appears to depend on a preferred affinity of these drugs for fungal versus mammalian cytochrome P-450 sterol demethylases. Enzyme inhibition by sulconazole prevents the synthesis of ergosterol, a sterol found in fungal cell membranes but, in general, not in mammalian cell membranes. Additionally, lanosterol accumulates, which changes membrane permeability, cell volume, secondary metabolic effects, and causes defective cell division and growth inhibition. As sulconazole is primarily fungistatic, an intact immune system may be needed for infection resolution.In selected situations, sulconazole may have growth phase-dependent fungicidal activity against very susceptible organisms. The 1% concentration of sulconazole may greatly exceed the minimum inhibitory concentration and exert a direct physiochemical effect on the fungal cell membrane. The fungicidal effect may be due to hydrophobic interactions between sulconazole and unsaturated fatty acids in the membrane. Mammalian cells generally have little or no unsaturated fatty acids. Sulconazole may also prevent DNA and RNA synthesis and increase their degradation.Sulconazole has activity against many dermatophytes and yeast. One measure of the drug's antifungal activity is the relative inhibition factor (RIF). The RIF approaches 0% for a drug to which a fungus is highly sensitive and 100% for a drug that is non-inhibitory. The RIF values of sulconazole for Candida species, Aspergillus species, and dermatophytes are broadly similar to those of clotrimazole, econazole, ketoconazole, miconazole, and tioconazole. The mean RIF values were 69% (30—98%) for Candida species, 71% (61—82%) for Aspergillus species, and 12% (5—18%) for dermatophytes. Sulconazole is available as a cream or solution to treat skin infections such as athlete's foot, ringworm, jock itch, and sun fungus.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3390824 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12611652 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | EXELDERM Approved UseEXELDERM (sulconazole nitrate, USP) CREAM, 1.0% is an antifungal agent indicated for the treatment of tinea pedis (athlete’s foot), tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis,* and for the treatment of tinea versicolor. Launch Date1989 |
|||
Curative | EXELDERM Approved UseEXELDERM (sulconazole nitrate, USP) CREAM, 1.0% is an antifungal agent indicated for the treatment of tinea pedis (athlete’s foot), tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis,* and for the treatment of tinea versicolor. Launch Date1989 |
|||
Curative | EXELDERM Approved UseEXELDERM (sulconazole nitrate, USP) CREAM, 1.0% is an antifungal agent indicated for the treatment of tinea pedis (athlete’s foot), tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis,* and for the treatment of tinea versicolor. Launch Date1989 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
4.81 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7320848 |
1000 mg single, oral dose: 1000 mg route of administration: Oral experiment type: SINGLE co-administered: |
SULCONAZOLE plasma | Canis lupus population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7320848 |
1000 mg single, oral dose: 1000 mg route of administration: Oral experiment type: SINGLE co-administered: |
SULCONAZOLE plasma | Canis lupus population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
1 % 2 times / day multiple, topical Recommended Dose: 1 %, 2 times / day Route: topical Route: multiple Dose: 1 %, 2 times / day Sources: Page: RS 44872 |
unhealthy, adult n = 286 Health Status: unhealthy Condition: Tinea pedis | Tinea cruris | Tinea corporis | Cutaneous candidiasis | Tinea versicolor Age Group: adult Sex: M+F Population Size: 286 Sources: Page: RS 44872 |
Disc. AE: Contact dermatitis, Pruritus... AEs leading to discontinuation/dose reduction: Contact dermatitis Sources: Page: RS 44872Pruritus |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Contact dermatitis | Disc. AE | 1 % 2 times / day multiple, topical Recommended Dose: 1 %, 2 times / day Route: topical Route: multiple Dose: 1 %, 2 times / day Sources: Page: RS 44872 |
unhealthy, adult n = 286 Health Status: unhealthy Condition: Tinea pedis | Tinea cruris | Tinea corporis | Cutaneous candidiasis | Tinea versicolor Age Group: adult Sex: M+F Population Size: 286 Sources: Page: RS 44872 |
Pruritus | Disc. AE | 1 % 2 times / day multiple, topical Recommended Dose: 1 %, 2 times / day Route: topical Route: multiple Dose: 1 %, 2 times / day Sources: Page: RS 44872 |
unhealthy, adult n = 286 Health Status: unhealthy Condition: Tinea pedis | Tinea cruris | Tinea corporis | Cutaneous candidiasis | Tinea versicolor Age Group: adult Sex: M+F Population Size: 286 Sources: Page: RS 44872 |
PubMed
Title | Date | PubMed |
---|---|---|
Topical pharmacology of imidazole antifungals. | 1976 |
|
Percutaneous absorption of sulconazole nitrate in humans. | 1988 Jun |
|
Comparison of the chiral resolution of econazole, miconazole, and sulconazole by HPLC using normal-phase amylose CSPs. | 2001 Aug |
|
Assessing pregnancy risks of azole antifungals using a high throughput aromatase inhibition assay. | 2002 Aug |
|
Comparative study of the enantiomeric resolution of chiral antifungal drugs econazole, miconazole and sulconazole by HPLC on various cellulose chiral columns in normal phase mode. | 2002 Jan 15 |
|
Inhibition of cytochromes P450 by antifungal imidazole derivatives. | 2002 Mar |
|
Topical antifungal treatment cures exit-site fungal infection. | 2002 Oct |
|
Identification and prediction of promiscuous aggregating inhibitors among known drugs. | 2003 Oct 9 |
|
In vitro susceptibility testing of dermatophytes: comparison of disk diffusion and reference broth dilution methods. | 2004 Apr |
|
Athlete's foot. | 2005 Dec |
|
Molecular properties of econazole and sulconazole relevant to bioavailability. | 2006 Sep-Oct |
|
Genome-wide fitness test and mechanism-of-action studies of inhibitory compounds in Candida albicans. | 2007 Jun |
|
1-[2-(2,4-Dichloro-benz-yloxy)-2-phenyl-ethyl]-1H-1,2,4-triazole. | 2008 Nov 29 |
|
1-[2-(2,6-Dichloro-benz-yloxy)-2-(2-fur-yl)eth-yl]-1H-1,2,4-triazole. | 2009 Dec 12 |
|
Enantioselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea organocatalysis. | 2009 Jul 1 |
|
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2. | 2011 Jul 14 |
|
The monoamine oxidase A inhibitor clorgyline is a broad-spectrum inhibitor of fungal ABC and MFS transporter efflux pump activities which reverses the azole resistance of Candida albicans and Candida glabrata clinical isolates. | 2012 Mar |
|
FDA-approved drugs and other compounds tested as inhibitors of human glutathione transferase P1-1. | 2013 Sep 5 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/ppa/sulconazole.html
Tinea corporis/tinea cruris/tinea versicolor: Topical: Apply a small amount to the affected and surrounding skin areas once or twice daily for 3 weeks
Tinea pedis: Topical: Cream: Apply a small amount to the affected area twice daily for 4 weeks
Route of Administration:
Topical
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23122865
HEK 293T cells were transfected with mouse Ido1, Ido2 or Tdo2 expression constructs for the enzymatic activity assay. One day after transfection the medium was replaced with phenol red-free medium supplemented with LTrp (1 mM for library screening or 400 lM for all other experiments). All compounds tested for effects on enzymatic activity were dissolved in dimethyl sulfoxide (DMSO) and added to the transfected cells, along with a DMSO control. On the following day, the protein in the medium was precipitated with the addition of trichloroacetic acid (final concentration 4%) and centrifugation at 1500 rcf, 10_ C for 45 min. Supernates were carefully removed and added to an equal volume of 2% (w/v) Ehrlich’s reagent, 4-(Dimethylamino) benzaldehyde in glacial acetic acid. Absorbances were measured at 485 nm using the SPECTRA MAX 190 microplate spectrophotometer (Molecular Devices, USA).
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:48:54 GMT 2023
by
admin
on
Sat Dec 16 04:48:54 GMT 2023
|
Record UNII |
1T89100D5U
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C514
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
1623681
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
CHEMBL1221
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
m10295
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | Merck Index | ||
|
92446-61-2
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
SUPERSEDED | |||
|
61318-91-0
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
DTXSID2045490
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
100000085066
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
757849
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
56798
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | RxNorm | ||
|
1T89100D5U
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
DBSALT001375
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
C47733
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
1T89100D5U
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
SUB04618MIG
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
65495
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
PRIMARY | |||
|
59293-82-2
Created by
admin on Sat Dec 16 04:48:54 GMT 2023 , Edited by admin on Sat Dec 16 04:48:54 GMT 2023
|
SUPERSEDED |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |