Inhibition of human testicular glucose-6-phosphate dehydrogenase by unsaturated C19-steroids

Zusammenfassung Die Bebrütung einer gereinigten G-6-PDH aus menschlichem Testisgewebe mit 3-substituierten ⁴- oder ⁵-C₁₉-Steroiden zeigte, dass 3-Hydroxy-⁴-oder ⁵-androsten-17-on auch wirksame Inhibitoren der testikulären G-6-PDH darstellen. Zur gleichen Zeit konnten die früher gefundenen Zusammenhänge zwischen chemischer Struktur eines Steroids und seiner biologischen Aktivität im G-6-PDH-Hemmtest uneingeschränkt bestätigt werden.     

Der durch circadiane Frequenzänderung entstehende Fehler bei der Bestimmung von Phasenverschiebungen

Summary Phase shifts () are commonly measured without considering the cue's phase position ( _s ). The normally adopted methods for measuring phase shifts give errorless results only when there is no change in period length (). Very often, however, both phase shifts and changes in period length occur together. The magnitude of the error is then a function of the magnitude of and the distance between the points of measurement and the cue's phase position. (The basic hypothesis is that is effected immediately after the cue.) Methods for calculating and eliminating the error are given.     

The distribution of some enzymes involved in the steroidogenesis of hen's ovary

Riassunto È stata studiata con metodi istochimici la distribuzione della ⁵-3-idrossisteroide deidrogenasi ( ⁵-3-HSDH) e delle 17-idrossisteroide deidrogenasi (17-HSDH), DPN- e TPN-dipendenti, nell'ovario di gallina ovulante. Mentre la ⁵-3-HSDH è presente in tutti i tessuti a secrezione steroide dell'ovario, la 17-HSDH è localizzata solo nelle cellule della granulosa.     

Thermodynamics of bromate and iodate of potassium in dioxane-water mixtures from conductance measurements

Summary The free energy of transfer ( G _t ⁰ ) of KBrO₃ and KIO₃ from water to 10, 20 and 30% dioxane-water mixtures have been studied from conductometric measurements. The G _t ⁰ values are in the order of BrO ₃ ^– >IO ₃ ^– .     

Hashish VI1: Conversion of (-)-Δ 1(6)-Tetrahydrocannabinol to (-)-Δ 1(7)-Tetrahydrocannabinol. Stability of (-)-Δ 1 and (-)-Δ 1(6)-Tetrahydrocannabinols

Zusammenfassung Die Synthese von (—)-¹⁽⁷⁾-Tetrahydrocannabinol (THC) auf (—)-¹⁽⁶⁾ wird beschrieben. Das Hauptprodukt der oxidativen Zerstörung von (—)-¹-THC ist Cannabinol. Beschleunigte Versuche der Luftoxidation von (—)-¹-THC und (—)-¹⁽⁶⁾-THC haben gezeigt, dass das letztere beständiger ist. Dieser Unterschied kann mit der Reaktivität des C₃-benzylisch-allylischen Wasserstoffes in (—)-¹-THC erklärt werden.     

(−)-Δ8-tetrahydrocannabinol: Two novel in vitro metabolites

Zusammenfassung (–)-⁸-Tetrahydrocannabinol ist einer der Aktivstoffe in Marihuana (Cannabis sativa L.). Inkubation dieser Verbindung mit der überstehenden Zentrifugationsfraktion (9000g) aus männlicher Hundeleber ergab zwei Hauptmetaboliten, welche durch Massenspektrometrie und Kernresonanzspektroskopie identifiziert wurden. Den beiden Verbindungen werden die Strukturen des 1-Hydroxy-⁸-tetrahydrocannabinols und des 3-Hydroxy-⁸-tetrahydrocannabinols zugeordnet.     

Zur Umsetzung von 3α-Hydroxy-5β-Steroiden mit Blei(IV)-acetat

Summary On treatment of 3-hydroxy-5-steroids with lead tetra-acetate formation of 3, 9-oxides is observed. The yields of this ring closure reaction decrease significantly in the order 11-keto, ^{9, 11}-ene and ring-C saturated compounds.     

The free radical oxidation of the tetrahydrocannabinols

Summary The free radical oxidation of ¹ and ⁶-tetrahydrocannabinol has been examined by spin trapping techniques and intermediates that would lead to cannabinol have been trapped. The 1st step in the oxidation of ¹-THC involves the removal of 3-H, while for ⁶-THC, either 2-H or 5-H. Intermediates were isolated which could be pyrolysed to the diene and cannabinol.     

Effect of 723-1723-1723-1on ethanol withdrawal in mice

Summary ⁹ (10 mg/kg, i.p.) administered to mice immediately after withdrawal from a 3-day exposure to ethanol vapor was found to intensify withdrawal reactions. No effect was seen when ⁹ was administered chronically during the exposure to ethanol.     

Wirkung von 6β-Methoxy-9β,10α-pregna-4,6-dien-3,20-dion

Summary 6-Methoxy-9,10 -pregna-4,6-diene-3,20-dione inhibites the ⁴-3-oxosteroid-5-reduction in microsomes and the ⁴-3-oxosteroid-5-reduction in the soluble fraction of male rat liver. The 3- and 3-hydroxysteroid dehydrogenase are not inhibited by this substance.

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Diese Arbeit wurde von der Firma Hoffmann-La Roche, Basel, unterstützt.     

Regulation ofL-valine absorption by opioids interacting withμ-receptors in rabbit ileum

In intact tissue, [d-Ala²,MePhe⁴, Gly-ol⁵] enkephalin (10^–5 M;-ligand), diminsihed short-circuit current (I_sc) and increased water, Na⁺ and Cl^– net fluxes in vitro under open circuit conditions; it also inhibitedL-valine absorption andL-valine-dependent variations of short-circuit current (I_{sc, val}). Naloxone (10^–6 M) antagonized these effects. In the absence of the muscularis and myenteric plexus this enkephalin or morphine (-ligand) reduced I_sc and I_{sc, val}. These enkephalin effects occurred at different times. Different concentrations of enkephalin were tested for their effects on I_{sc, val}. [d-Ala²,d-Leu⁵] enkephalin (mainly a -ligand) significantly decreased I_sc but not I_{sc, val}. The reduction ofL-valine absorption does not depend on the effects on basal ion transport. Interaction of opioids with-receptors located in the submucosal plexus and/or in the epithelial cell accounts for this reduction. This enkephalin effect seems to be at least partially under the control of the myenteric plexus.     

Ein neues Verfahren zur Herstellung von 19-Norsteroiden

Summary The new methods for the production of 19-norsteroids described involve the conversion of 5-halogen-6-hydroxy-steroids into the corresponding 5-halogen-6:19-ethers either with lead tetraacetate or by the hypoiodite reaction^8,10. The 6:19-oxygen bridge is then opened reductively either directly or after oxidation of the 6:19-ethers to lactones or preferably after introduction of a ^4,6-3-oxo grouping. Acylolytic cleavage of the ⁴-3-oxo-6:19-ethers followed by alkaline hydrolysis gives ^4,6-3-oxo-19-hydroxy-steroids. The 19-hydroxycompounds formed are easily converted into 19-norsteroids by known methods.

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Über Steroide, 189. (vorläufige) Mitteilung; 188. Mitt. vgl.J. Kalvoda, J. Schmidlin, G. Anner undA. Wettstein, Exper.18, 398 (1962).     

1,2-Methylen-19-nor-17α-acetoxy-progesteron

Summary The syntheses and structure-determinations of 1, 22- and 1, 2-methylene-19-nor-17-acetoxy-progesterones described prove that there is no influence of the angular C₁₀-methylgroup on the steric course of theCourey-methylenations of ¹-3-keto-steroids.     

Δ6-Tetrahydrocannabinol-7-oic acid,a urinary Δ6-THC metabolite: Isolation and synthesis

Zusammenfassung 7-Hydroxy- ⁶-tetrahydrocannabinol (7-Hydroxy- ⁶-THC), ein psychotomimetisch aktiver Metabolit des ⁶-THC, wird von Kaninchen in inaktive ⁶-THC-7 Säure metabolisiert. Die Synthese dieser Säure wird beschrieben.

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The work in Jerusalem was supported by the US National Institute of Mental Health and in Stockholm by the Swedish Medical Research Council.     

Mikrobiologische Oxydation von Steroiden durch Cephalosporia

Summary It was found that members of the Cephalosporium species transform steroids under the known conditions of microbiological oxydation. Cephalosporium subverticillatum is able to produce ⁴-testoloactone from progesterone, but, in case of a longer fermentation period, ⁴-androsten-3, 17-dione can be isolated from the broth.     

Effect of acute administration of Δ1-tetrahydrocannabinol on β-endorphin levels in plasma and brain tissue of the rat

Summary Acute treatment with ¹-tetrahydrocannabinol (¹-THC) elevated the concentration of -endorphin-like immunoreactivity (-ELIR) in plasma and in the hypothalamus, but not in the hippocampus of rats habituated to the injection procedure. These effects were not obtained with the psychotropically inert analog of (¹-THC), cannabidiol. In animals that had not been habituated to the injection procedure, placebo treatment induced a decrease in hippocampal -ELIR.The authors acknowledge the skillful technical assistance of Mrs Willeke Logtenberg.     

Volatiles from clover headHypera meles (Fab.) and alfalfaH. postica (Gyllenhal) weevils: search for pheromones

Summary Volatile fractions of the clover head,Hypera meles (Fab.), and alfalfa,Hypera postica (Gyllenhal), weevils contained three of four boll weevil,Anthonomus grandis (Boh.), pheromone components, (Z)-3,3-dimethylcyclohexane ^1,-ethanol and (Z)- and (E)-3,3-dimethylcyclohexane-^1,-acetaldehyde. Also found were eight oxygenated monoterpenes, previously identified as precursors and intermediates of the boll weevil pheromones.     

Isomeric homoallylic cations formed from 19-substituted steroids

Zusammenfassung Die Existenz von zwei verschiedenen isomeren Homoallylkationen in der Umlagerung von Steroid- ⁵-19-Methansulfonsäure-Estern zu 5, 19-cyclo-6-hydroxylierten Steroiden und deren Umlagerung zu ⁵(¹⁰)-B-homo-7-hydroxylierten Steroiden wurde bewiesen, und eine neue Art der Homoallylumlagerung eines ⁵(¹⁰)-B-homo-7-hydroxylierten Steroids zum 5, 6-Methano-9-en und zum 5, 6-Methano-10-ol wurde beobachtet.

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This material was presented at theSymposium on Steroids Made Through Intramolecular Functionalization on the C ₁₈-and C ₁₉-Methyl Groups, at the 149th meeting of the American Chemical Society in Detroit (Michigan), on April 7, 1965.     

416-1416-1416-1416-2416-2416-2

Summary (–)-8-Hydroxymethyl-¹-tetrahydrocannabinol (THC)1, a novel analog of ¹, is shown to be as active as ¹ and twice as active as ¹ in the dog ataxia test.Acknowledgment. This work was supported by NIDA (Grant Nos. DA-00574-01 and DA-00490).