| Weight | 492.146 g/mol |
|---|---|
| Formula | C18H14Cl4N4O4 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 6 |
Oxiconazole nitrate (64211-46-7)
oxiconazole · Salongo · Oxistat
Score:
#2 in Mycology
,
#14 in Medicinal chemistry
,
#382 in Microbiology
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#2985 in Biology
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- Synthesis, Antifungal Activity, and Molecular Modeling Studies of New Inverted Oxime Ethers of Oxiconazole (Journal of Medicinal Chemistry, 2002)
- 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)
- Tetrahydronaphthyl azole oxime ethers: The conformationally rigid analogues of oxiconazole as antibacterials (European Journal of Medicinal Chemistry, 2009)
- Nail penetration of the antifungal agent oxiconazole after repeated topical application in healthy volunteers, and the effect of acetylcysteine (European Journal of Pharmaceutical Sciences, 1997)
- Oxiconazole, a new imidazole derivative. Evaluation of antifungal activity in vitro and in vivo. (Drug Research, 1982)
- Effect of oxiconazole and Ro 14-4767/002 on sterol pattern in Candida albicans (Medical Mycology, 1985)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - oxiconazole
- Salongo
- Oxistat
- Sgd 301-76
- Oxizole
- (Z)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-O-(2,4-dichlorobenzyl) ethanone oxime nitrate
- Fonx
- oxiconazole mononitrate, (Z)-isomer
- Oceral
- RO-13-8996
- oxyconazole
- Myfungar
- Gyno-Myfungar
-
SMILESC1=CC(=C(C=C1Cl)Cl)CON=C(CN2C=CN=C2)C3=C(C=C(C=C3)Cl)Cl.[N+](=O)(O)[O-]
-
InChIKeyWVNOAGNOIPTWPT-UHFFFAOYSA-N
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Oxiconazole nitrate
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