Weight | 397.758 g/mol |
---|---|
Formula | C18H15Cl3N2S |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 3 |
Rotatable Bonds | 6 |
sulconazole (61318-90-9)
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- Antifungal relative inhibition factors: BAY 19139, bifonazole, butoconazole, isoconazole, itraconazole (R 51211), oxiconazole, Ro 144767/002, sulconazole, terconazole and vibunazole (BAY n-7133) compared in vitro with nine established antifungal agents (Journal of Antimicrobial Chemotherapy, 1984)
- 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. (Journal of Pharmaceutical and Biomedical Analysis, 2002)
- Comparison of the chiral resolution of econazole, miconazole, and sulconazole by HPLC using normal-phase amylose CSPs (Fresenius Journal of Analytical Chemistry, 2001)
- A doubleblind comparison of sulconazole nitrate 1% cream with clotrimazole 1% cream in the treatment of dermatophytoses (British Journal of Dermatology, 1983)
- Theoretical approach in the study of the inclusion processes of sulconazole with -cyclodextrin (Journal of Molecular Liquids, 2010)
- 1% sulconazole cream v 2% miconazole cream in the treatment of tinea versicolor. A double-blind, multicenter study. (Archives of Dermatology, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1CSC(CN2C=CN=C2)C3=C(C=C(C=C3)Cl)Cl)Cl
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InChIKeyAFNXATANNDIXLG-UHFFFAOYSA-N
- Pubchem - sulconazole
- Wikipedia - sulconazole
Sulconazole (trade name Exelderm) is an antifungal medication of the imidazole class. It is available as a cream or solution to treat skin infections such as athlete's foot, ringworm, jock itch, and sun fungus. Although not used commercially for insect control, sulconazole nitrate exhibits a strong anti-feeding effect on the keratin-digesting Australian carpet beetle larvae Anthrenocerus australis.
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