Silymarin,an inhibitor of lipoxygenase

Summary Silybin (I), silydianin (II) and, silychristin (III), the main constituents, of silymarin, non-competitively inhibit the lipoxygenase from soybeans (EC 1.13.11.12) in vitro.F. Fiebrich, Thesis, University of Vienna 1977.H. Koch, Dt. ApothZtg118, 1844 (1978); reported in part at the Colloquium Pharmaceuticum in Münster, 21 st November 1978.     

Presence in immunostimulated cells of an RNA molecule utilizable as template for reverse transcriptase of avian myeloblastosis virus (AMV)]

Cytoplasmic RNA extracted from antigen stimulated immunocompetant cells is transcribed in vitro into DNA by the RNA directed DNA polymerase from avian myeloblastosis virus, in the absence of any added primer. Cytoplasmic RNA from other organs of the same animal, from non-stimulated immunocompetent cells, or from cells in tissue culture is not transcribed in the absence of exogenous primer.     

Silymarin,an inhibitor of prostaglandin synthetase

Summary Silybin (I), silydianin (II) and silychristin (III), the main constituents of silymarin, inhibit the formation of prostaglandins in vitro. The inhibition is log-linearly dependent on the concentration of the effectors.F. Fiebrich, Thesis, University of Vienna 1977.H. Koch, Dt. ApothZtg118, 1844 (1978); reported in part at the Colloquium Pharmaceuticum in Münster, 21st November 1978.     

Sodium azide,an efficient inhibitor of protein diazotization

Résumé L'azide de sodium est un inhibiteur très efficace de la réaction de diazotation. Il réagit avec l'ion de diazonium à des molarités approximativement égales.     

Chromatographic separation of an inhibitor reversibly associated with fibrinolysin in the serum of guinea-pig

Riassunto Il solfato di cellulosa attiva l'enzima fibrinolitico del siero di cavia in soluzione neutra, a differenza di altri poliacidi che sono attivatori a basso pH. È proposto un meccanismo per l'attivazione basato sull'interazione fra il poliacido e l'inibitore. L'inibitore è stato separato dalle globuline di cavia per cromatografia a scambio di ioni.     

Cell kinetic studies in the epidermis of the mouse. I. Changes in labeling index with time after tritiated thymidine administration

The changes in the labeling index (LI) with time after a single injection of tritiated thymidine (3HTdR) at each of 4 different times of the day have been studied. Slight differences occur in the shape of these LI curves, (e.g. in the timing of the peaks) depending on the time of day when the initial injection was given. Thus, the time of day influences not only the number of cells in DNA synthesis but also determines the subsequent behavior of the labeled cells. The curves show 3 distinct peaks from which estimates of the cell cycle time can be made. The technique permits the cell cycle time to be estimated. From the data as a whole a minimum cell cycle time of 90 h for basal cells in the epidermis on the back of a mouse is obtained. The technique also provides estimates for the duration of S + G2 + M which varies depending on the time of day that the label is given. The LI curves can best be understood if the basal layer is assumed to contain 2 cell populations with differing cell cycle times; one having a long cell cycle (about 180 h) but short S-phase and containing the stem cells, the other having a short cell cycle (about 90 h) and a long S-phase duration and consisting of transit cells.     

Isolation of a hexaprenylhydroquinone sulfate from the marine sponge Dysidea sp. as an H,K-ATPase inhibitor

A hexaprenylhydroquinone sulfate has been isolated as an H,K-ATPase inhibitor from a marine sponge Dysidea sp. It also inhibited phospholipase A2 as well as secretion of gastric acid in rats.     

Narciclasine,an inhibitor of protein synthesis. Action onAllium cepa L. root meristems

Summary Shortening of nucleologenesis time in a synchronous cell population, labelled as binucleate, by a caffeine pulse and fall in frequency of prophases are related to narciclasine inhibition of protein synthesis inAllium cepa L. meristems.Acknowledgments. We gratefully acknowledge Dr D. Vázquez and Dr A. Jiménez, from the Instituto de Bioquímica de Macromoléculas, for calling our attention to this protein synthesis inhibitor and providing us samples both of narciclasine andNarcissus bulbs. We also greatly appreciate Dr B. Rodriguez and Dr F. M. Panizo of the Instituto de Química Orgánica (Departamento de Productos Naturales) for their valuable help in isolation and characterization of narciclasine, and for laboratory facilities. The work has been partially supported by the Comisión Asesora para la Investigación Científica (Spain). A.S. has a fellowship awarded by the Instituto de Cultura Hispánica, Spain.     

Thoruranium (U-236) as the extinct natural parent of thorium: The premature falsification of an essentially correct theory

To explain the origin of thorium, the Austrian geophysicist Kirsch in 1922 postulated a hypothetical isotope, thoruranium (U-236), by analogy with actinouranium. The theoretical life-time of thoruranium was predicted as being too short for it to have survived in the recent geological past. Available geological data was not inconsistent with this hypothesis, but neither did it confirm it. Within five years one new piece of geological evidence, which appeared not to conform with predictions based upon this alleged U-236, was accepted even by Kirsch as sufficient to falsify his theory. However, during the 1940s, U-236 was produced artificially, and its characteristics were found to conform with those postulated for thoruranium. Subsequent research on the origin of the universe has confirmed that indeed a natural endowment of U-236 did once exist in considerable abundance.     

Novel substrates for the kinetic assay of esterases associated with insecticide resistance

Naphthalene thioesters were synthesized as substrates for a continuous, non- disruptive kinetic assay of general carboxylesterase activity. The continuous nature of the assay is based on the production of a soluble dianion chromophore from the reaction of naphthalene thio with 5,5-dithiobis (2-nitrobenzoic acid). Applications with 1- and 2-naphthalene thioacetates demonstrated their use in a fast accurate kinetic microassay of esterase activity, using porcine carboxylesterase as a model. These novel esters proved to be useful as substrates for the spectrophotometric assay of insecticide-resistance in two aphid species and may be applicable to other esterasebased diagnostic procedures.