Method of treating fungal infections using sterodial ester compounds

PCT No. PCT/GB90/00699 Sec. 371 Date Nov. 4, 1991 Sec. 102(e) Date Nov. 4, 1991 PCT Filed May 4, 1990 PCT Pub. No. WO90/13298 PCT Pub. Date Nov. 15, 1990.Compounds of the general formula (2): (2) wherein X is a hydrogen atom or a hydroxyl group, Y is a hydrogen atom or a hydroxyl group and R is an a...

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Hauptverfasser:	MARPLES, BRIAN A, STRETTON, REGINALD J
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Sprache:	eng
Schlagworte:	CHEMISTRY HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS STEROIDS
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creator	MARPLES BRIAN A STRETTON REGINALD J
description	PCT No. PCT/GB90/00699 Sec. 371 Date Nov. 4, 1991 Sec. 102(e) Date Nov. 4, 1991 PCT Filed May 4, 1990 PCT Pub. No. WO90/13298 PCT Pub. Date Nov. 15, 1990.Compounds of the general formula (2): (2) wherein X is a hydrogen atom or a hydroxyl group, Y is a hydrogen atom or a hydroxyl group and R is an alkyl group of 1 to 4 carbon atoms, have anti-fungal activity, especially against organisms selected from Candida spp. and the athlete's foot organism Trichophyton mentagrophytes and the ringworm organism Microsporum audonii. Further, the compounds wherein X and R are hydrogen atoms and Y is a hydroxyl group (or its non-toxic salts) are useful against Microsporum audonii.
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Date Nov. 15, 1990.Compounds of the general formula (2): (2) wherein X is a hydrogen atom or a hydroxyl group, Y is a hydrogen atom or a hydroxyl group and R is an alkyl group of 1 to 4 carbon atoms, have anti-fungal activity, especially against organisms selected from Candida spp. and the athlete's foot organism Trichophyton mentagrophytes and the ringworm organism Microsporum audonii. 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No. WO90/13298 PCT Pub. Date Nov. 15, 1990.Compounds of the general formula (2): (2) wherein X is a hydrogen atom or a hydroxyl group, Y is a hydrogen atom or a hydroxyl group and R is an alkyl group of 1 to 4 carbon atoms, have anti-fungal activity, especially against organisms selected from Candida spp. and the athlete's foot organism Trichophyton mentagrophytes and the ringworm organism Microsporum audonii. Further, the compounds wherein X and R are hydrogen atoms and Y is a hydroxyl group (or its non-toxic salts) are useful against Microsporum audonii.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record>
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subjects	CHEMISTRY HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS STEROIDS
title	Method of treating fungal infections using sterodial ester compounds
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