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).     

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.     

Tolerance to,and symmetrical cross-tolerance between,cannabionol and 295-1295-1295-1

Summary Tolerance to, and symmetrical cross-tolerance between, cannabinol and ⁹-tetrahydrocannabinnol (THC) occurs in rabbits which uniquely exhibit behavioral convulsions with THC.This research was supported by funds (grant No.DA01448) and cannabinoids from the National Institute on Drug Abuse.     

(−)-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.     

A novel cannabinoid containing a 1,8-cineol moiety

Summary The synthesis of a novel cannabinoid containing a 1,8-cineol moiety (1) is described. It is much less biologically active than ¹-tetrahydrocannabinol.Acknowledgment. This work was supported by NIDA (grant No. DA-00574-01).     

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.     

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.     

Decrease of serum alpha-tocopherol levels in rabbits after acute treatment withΔ 9-tetrahydrocannabinol

Summary The i.v. administration of 10 mg of ⁹-THC in rabbits produced, after 24 h, a 50% reduction of the initial values of serum alpha-tocopherol.Grant of the Italian Ministry of Health, Service of Social Medicine; thanks are due to Dr O. J. Braenden, Director, UN Narcotics Laboratory at Geneva, for the gift of pure ⁹-THC.     

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.     

Synthesis of 3-(2′-chloroethoxy)-6-formyl-Δ3,5-pregnadienes. A new class of highly active anti-inflammatory corticosteroids

Riassunto È stata studiata 1'azione del reattivo di Vilsmeier-Haack su 3-cicloetilendiossi- ⁵-steroidi appartenenti ai corticoidi; è stata così ottenuta una scrie di 3-(2-cloroetossi)-6-formil- ^3,5-pregnadieni, alcuni dei quali hanno mostrato notevoli proprietà antiinfiammatorie con una netta dissociazione dell'attività per somministrazione locale e somministrazione sistemica.     

10-Hydroxy-Δ2-decenoic acid in the honeybee(Apis mellifera)

Zusammenfassung Die Mandibulardrüsen der Honigbienen-Arbeiterinnen enthalten 10-Hydroxy-²-decensäure. Es wird angenommen, dass diese Drüsen die Quelle der im Weisel- und Arbeiterinnenlarvenfutter vorkommenden 10-Hydroxy-²-decensäure sind.     

The molecular structure of the benzilic acid rearrangement product of 3α, 17β-diacetoxy-11-hydroxy-12-oxo-5β-androst-9(11)-ene

Zusammenfassung Die Struktur desp-Brombenzoates des Benzilsäureumlagerungsproduktes von 3, 17-Diacetoxy-11-hydroxy-12-oxo-5-9(11)-androsten wurde durch dreidimensionale Röntgenstrukturanalyse eines Einkristalls als 3-p-Brombenzoat des 11-Carboxy-3, 11, 17-trihydroxy-13-C-nor-5-androstan 11a, 17-Laktons erkannt.     

Thermodynamics of adsorption and desorption of hydrogen sulfide in micropores of activated carbon

Summary Thermodynamics of adsorption and desorption of hydrogen sulfide in micropores of activated carbon have been studied on the basis of q and S. The values of q and S of adsorption were larger than those of desorption.     

Structural changes accompanying the reversible cold inactivation of glyceraldehyde-3-phosphate dehydrogenase from rat skeletal muscle

qm -3- , 4° 0,15M NaCl, 5M , 4M - pH=7,6, ( 275–295 , –b _o , A ₁₉₃ , –A₂₂₅). , +20° 0.15M H₂PO₄.     

Chemical investigation of Indian soapnut,Sapindus laurifolius vahl.

Zusammenfassung Aus der Fleischschale der Nüsse vonSapindus laurifolius wurden ausser Hederagenin 2 Triterpene isoliert. Das eine wurde als Oleanolsäure identifiziert, und das andere (Sapindic-Säure) erwies sich als ¹² 3,23-oxido-oleanen-28-säure.     

Deamination by ‘Transformed’ mitochondrial amine oxidase of the ε-amino group of lysine and selective inhibition of this reaction by β-aminopropionitrile

« » - . -.     

Hashish: Synthesis of Δ9-tetrahydrocannabinol (THC), a metabolite ofΔ 9-THC1

Summary The synthesis of (±)-211-dihydroxy- ⁹-THC, a difunctionalized metabolite of ⁹-THC, is presented.Acknowledgment. This work was carried out with the support of NIDA Grant No. DA 00574. We are grateful to Mr. J. Coe for assistance with some of the experiments.     

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.     

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.     

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).