Christian-Albrechts-Universitaet Zu Kiel

Gruenenthal Gmbh

Christian-Albrechts-University of Kiel

Christian-Albrechts-Universitat Zu Kiel

Dieter Heber

Bernd Clement

Ullvi Bluhm

Bernd Sundermann

Hagen-Heinrich Hennies

Helmut Buschmann

Christopher Meier

Franz Furkert

Britta Gerig

Lars Stenzel

Uwe Buss

Friederike Friedrich-Harder

Ulrich Wolschendorf

Friederike Friedrich

The invention relates to the use of a substance of the general form (I) to produce an antibacterial and/or antifungal drug, wherein X is a methylene group or a carbonyl group; R, R, and Rare each selected from the group comprising hydrogen, an alkyl group having a chain length of 1-4 carbon atoms, an alkoxy group having a chain length of 1-3 carbon atoms, and a halogen; Rand Rare each selected from the group comprising hydrogen and an alkyl group having a chain length of 1-4 carbon atoms; and n=3 to 6. 

Antibacterial and antifungal biphenylyl compounds

New phenanthroline derivatives as drug as well as methods for producing said compounds are provided.

Pyrido [3,4-C] [1,9] phenanthroline and 11, 12 dihydropyrido [3,4-C] [1,9] phenanthroline derivatives and the use thereof, particularly for treating cancer

Use of the substance characterized by general structural formula (I) for the preparation of an agent inhibiting the enzymatic activity of NO-synthase, R1, R2, R3, R4 and/or R5 being hydrogen, an alkyl group, an aryl group or a heterocyclic group and n equals 2 or 3.

Basic acetophenones as inhibitors of NO-synthases

The invention relates to substituted pyrido[1,2-a]pyrimidine compounds corresponding to formula (I) wherein:

Substituted pyrido(1,2-a)pyrimidines and their use as NOS inhibitors

Growing community of inventors

Molfsee, Germany

Dieter Heber