Abstract:
A diagnostic aid for the scintigraphic visualization of malignant tumors which contains a radionuclide which is bonded by means of a complex-forming agent to the substance obtained by the enzymatic processing of murein with enzyme consisting essentially of hen's eggwhite lysozyme.
Abstract:
Streptomyces spec. DSM 3813 produces novel compounds with a basic phenoxazinone structure, which have an antifungal and antiviral action and can be used as lipoxygenase inhibitors.
Abstract:
The invention relates to cephem derivatives of the general formula I ##STR1## and their physiologically acceptable acid addition salts, to pharmaceutical formulations active against bacterial infections, to processes for preparing the compounds and formulations, and to the use of the compounds for combating bacterial infections.
Abstract:
A device for winding or unwinding of a cord-shaped material on and off a spool, respectively, with a spool support unit comprising two adjustable sleeves and a drive mechanism for rotating the spool, and with the spool support unit being suspended on a carrier. The support unit is mounted on the carrier rotatable out of its operating position by at least 90.degree. around a vertical axis.
Abstract:
A compensating storage for cable or the like comprising a group of rollers fixed on a frame and a group of compensating rollers moveable on horizontal rails, the compensating rollers being loaded by a storage tensioning device, whereby the cable is wound around both groups of rollers as a pulley rope. Support rollers for the upper cable strands are arranged between both groups of rollers, the support rollers being moveable on horizontal rails. The support rollers on the one hand lie in the path of movement of the inwardly moving compensating rollers and are able to be pushed together by the latter, and on the other hand are able to be drawn apart from one another by towing members which are connected to the compensating rollers.
Abstract:
The disclosure relates to a compound of the formula (I) wherein R1 is H, C(O)—(C1-C6)alkyl or C(O)—O—(C1-C6)alkyl; R2 is OH, NH2, NH—(C1-C6)alkyl, NH—(C1-C4)alkylene-phenyl or NH—(C1-C4)alkylene-pyridyl; R3 and R4 are independently of each other H or OH, or R3 and R4 together are ═O; and m and n are independently of one another 0, 1 or 2; in any stereochemical form, or a mixture of any stereochemical forms in any ratio, or a physiologically acceptable salt thereof, obtainable from Actinomadura namibiensis (DSM 6313), and its use for the treatment of bacterial infections, viral infections and/or pain, and pharmaceutical composition comprising it.
Abstract:
The disclosure relates to a compound of the formula (I) wherein m and n are independently of one another 0, 1 or 2, obtainable from Actinomadura namibiensis (DSM 6313), its use for the treatment of bacterial infections, viral infections and/or pain, and pharmaceutical composition comprising it.
Abstract:
A device for making a wire strand with changing twist direction (SZ-stranding) from individual wires, includes a fixed guide (1) provided with bores for receiving the individual wires and a plurality of spaced apart storing disks (4) capable of being driven in changing directions and also having bores for receiving the individual wires to be stranded, and a laying disk (6) capable of being driven via drive disks (7) and transmission members (9), with a drive (8) common to at least a portion of the drive disks (7) being provided, wherein between the drive (8) and the drive disks (7) there is disposed a torsionally elastic shaft (15) having an arbitrary cross-section.
Abstract:
A new microorganism for breaking down moenomycins, a process for the breakdown, and the use of the breakdown products are disclosed. A new Bacillus species and the appropriate enzymes obtained therefrom can be used to break down phosphoglycolipid antibiotics. The breakdown products of moenomycins display antibiotic activity or can be used as building blocks for the synthetic preparation of transglycosylase inhibitors.
Abstract:
A new Bacillus species and the appropriate enzymes obtained therefrom can be used to break down phosphoglycolipid antibiotics. The breakdown products of moenomycins display antibiotic activity or can be used as building blocks for the synthetic preparation of transglycosylas inhibitors.