Hoechst Aktiengesellschaft

Aventis Pharma Deutschland, Gmbh

Aventis Pharma S.a.

Medicis Pharmaceutical Corporation

Astrid Markus

Manfred Bohn

Karl Theodor Kraemer

Laszlo Vertesy

Joachim Wink

Laurent Schio

Patrick Fauveau

Jean-Marc Michel

Dominique Melon Manguer

Olivier Courtin

Gerhard Seibert

Michael Kurz

Herbert Kogler

Wilhelm Stahl

Uwe Gerlach

Rudolf Lattrell

Johannes Meiwes

Peter Hammann

Michael Limbert

Norbert Krass

Matthias Schiell

Rolf Horlein

L&aacute;szl&oacute; Vertesy

Theo Wollmann

Heike Stump

J&uuml;rgen Backhaus

Compounds of the formula (I) are disclosed and are suitable for the treatment of seborrheic dermatitis. 

Use of 1-hydroxy-2-pyridones for the treatment of seborrheic dermatitis

Compounds of the formula wherein the substituents are as defined in the application useful as antifungal agents.

Echinocandin derivatives, their method of preparation and their application as anti-fungal agents

Compound of the formula wherein Ris &#x2014;CH&#x2014;CH&#x2014;NH, Ris &#x2014;CH, Ris &#x2014;OH, R is Z is methyl and salts thereof which are useful as antifungal agents.

A pharmaceutical preparation comprising a hydrophilic gel-forming agent, water and a compound of the formula Iis suitable for the treatment and prophylaxis of dermatomycoses.

Antimycotic gel having high active compound release

Antimycotic gel with high active substance release

A compound of Formula I in which R and R &equals;H, OH, alkyl optionally substituted, or NR forms with the carbon bearing NR R a double bond and R is Xra, X being O, NH or N-alkyl and Ra being H, alkyl optionally substituted; R&equals;a chain containing up to 10 carbon atoms, optionally comprising one or several heteroatoms, one or several heterocycles; T&equals;H, CH , CH CONH , CH C&equiv;, (CH ) NH ; Y&equals;H, OH, halogen; W&equals;H, OH; Z&equals;H or CH ; said products have antifungal properties.

Echinocandin derivatives, preparation method and application as anti-fungal agents

Memno peptides, process for their preparation and use thereof

Use of 1-hydroxy-2-pyridones for the treatment of skin diseases

Antifungal peptides from scleroderma texense

The invention relates to lipopeptides with very homologous amino-acid sequences but different fatty acid residues (lipid portion) which are synthesized by Actinoplanes sp. during fermentation and are released into the culture medium, to a process for isolating the lipopeptides from the culture medium and purifying them, to the use of the lipopeptides as pharmacologically active substances, in particular against Gram-positive bacteria, and to Actinoplanes sp. DSM 7358 for producing the abovementioned lipopeptides.

Lipopeptides from actinoplanes sp. with pharmacological action, process for their production and the use thereof

Use of glyceryl triacetate for treating onychomycoses

The present invention relates to bismuth salts of antibiotics of the moenomycin group, processes for their preparation, their use and pharmaceuticals comprising such salts. The salts according to the invention contain antibiotics of the moenomycin group which are so-called phosphoglycolipid antibiotics and which are present individually or as a mixture, or derivatives thereof, and bismuth in defined stoichiometric ratios. They are outstandingly suitable, in particular, for controlling Helicobacter pylori and, thus, for example, for the therapy and prophylaxis of gastric disorders.

Bismuth salts of antibiotics of the moenomycin group, processes for

Novel polyene antibiotics, 3874 H1 to H6, processes for their preparation and use which are suitable for treating fungal diseases, trichomonad diseases, and for treating diseases associated with an increased steroid concentration.

Polyene antibiotics, 3874 H1 to H6, processes for their preparation and

Tetracyclic antibiotics and processes for their preparation .beta.-Lactam antibiotics of the formula I, and their pharmaceutically tolerable salts ##STR1## where X is (CH.sub.2).sub.0-2, CR(a)R(b), O, SO.sub.0-2 or NR(c),

Tetracyclic antibiotics and processes for their preparation

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Liederbach, Germany

Astrid Markus