Sulconazole mononitrate
Sulconazole mononitrate structure
|
Common Name | Sulconazole mononitrate | ||
|---|---|---|---|---|
| CAS Number | 61318-91-0 | Molecular Weight | 460.76200 | |
| Density | N/A | Boiling Point | 558.2ºC at 760 mmHg | |
| Molecular Formula | C18H16Cl3N3O3S | Melting Point | 130.5-132℃ | |
| MSDS | Chinese USA | Flash Point | 291.4ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
Effect of (+) or (-) camphorsulfonic acid additives to the mobile phase on enantioseparations of some basic drugs on a Chiralcel OD column.
J. Chromatogr. A. 1083(1-2) , 133-40, (2005) This paper describes the modification of Chiralcel OD column properties by adsorption of (+) or (-) camphorsulfonic acids (CSAs) used as additives to the mobile phase. The effects on retention, selectivity and efficiency, of adsorption of (+) and (-) CSAs on ... |
|
|
Athlete's foot.
Clin. Evid. (14) , 2000-5, (2005)
|
|
|
Direct lethal action of sulconazole and butoconazole.
Ann. Dermatol. Venereol. 118 Suppl 1 , 5-6, (1991)
|
|
|
In vitro activity of cloconazole, sulconazole, butoconazole, isoconazole, fenticonazole, and five other antifungal agents against clinical isolates of Candida albicans and Candida spp.
Mycopathologia 118(1) , 15-21, (1992) The in vitro activity of several new imidazoles, cloconazole, sulconazole, butoconazole, isoconazole and fenticonazole, were compared with those of amphothericin B, flucytosine, and three azoles: econazole, miconazole and ketoconazole against isolates of path... |
|
|
Enantioselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea organocatalysis.
J. Am. Chem. Soc. 131(25) , 8754-5, (2009) The highly enantioselective addition of thioacetic acid to nitroalkenes using a new sulfinyl urea organocatalyst is described. The addition of thioacetic acid proceeds in high yields and enantioselectivities for a variety of aromatic and aliphatic nitroalkene... |
|
|
[Determination of hemolytic activity and in vitro antifungal susceptibility of Trichophyton rubrum clinical strains].
Mikrobiyol. Bul. 45(1) , 159-67, (2011) Trichophyton spp. which are among the agents of dermatophytosis with high morbidity, produce many virulence factors including hemolysins that exhibit toxic activity on immune system cells. Since relapses and chronicity are common problems related to dermatoph... |
|
|
Comparison of the chiral resolution of econazole, miconazole, and sulconazole by HPLC using normal-phase amylose CSPs.
Fresenius J. Anal. Chem. 370(7) , 951-5, (2001) Resolution of the enantiomers of (+/-)-econazole, (+/-)-miconazole, and (+/-)-sulconazole has been achieved on different normal-phase chiral amylose columns, Chi-ralpak AD, AS, and AR. The mobile phase used was hexane-2-propanol-diethylamine, 400:99:1 (v/v). ... |
|
|
Allergic contact dermatitis due to sulconazole.
Contact Dermatitis 26(4) , 281-2, (1992)
|
|
|
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.
J. Pharm. Biomed. Anal. 27(3-4) , 441-6, (2002) The chiral resolution of (+/-)-econazole, (+/-)-miconazole and (+/-)-sulconazole on the columns containing different cellulose derivatives namely Chiralcel OD, OJ, OB, OK, OC and OF in normal phase mode has been described. The mobile phase used was hexane-2-p... |
|
|
EpoK, a cytochrome P450 involved in biosynthesis of the anticancer agents epothilones A and B. Substrate-mediated rescue of a P450 enzyme.
Biochemistry 43(46) , 14712-21, (2004) The epothilones are a new class of highly promising anticancer agents with a mode of action akin to that of paclitaxel but with distinct advantages over that drug. The principal natural compounds are epothilones A and B, which have an epoxide in the macrocycl... |