Structure and stereochemistry of attenuol,a new lignan fromKnema attenuata (Wall.) Warb.

Summary A new lignan attenuol has been isolated from the bark ofKnema attenuata (Wall.) Warb. Its structure (I) is deduced on the basis of analytical and spectral data. The compound has been assigned the absolute configuration as 2S,3R-dimethyl-1S-(p-hydroxyphenyl)-6,7-methylenedioxytetralin (III).Contribution No. 487 from the Ciba-Geigy Research Centre.Acknowledgments. We thank Dr H. Fuhrer and Dr P. Moser of Ciba-Geigy Ltd. Basle for the NMR spectral data and ORD determinations and Dr S. Selvavinayakam and his colleagues for the analytical results.     

New tigliane and daphnane derivatives fromPimelea prostrata andPimelea simplex

Summary From the methanol extract ofPimelea prostrata, prostratin (I) and 2 autoxidation products have been isolated. They are tigliane derivatives and relatively nonirritant on the mouse ear. The irritant pimelea factor P₅ (IIa) also with a tigliane skeleton and related to mancinellin (IIb), as wellas the irritant diterpene ester pimelea factor P₁ (IIa, simplexin) with daphnane skeleton, were found to be present in bothP. prostrata andP. simplex. Further the irritant homologue of simplexin, pimela factorIIIb was detected inP. prostrata. Some biogenetic consequences of these findings are discussed.Acknowledgment: The authors are deeply indebted to Dr T. Cashmore (Palmerton North, New Zealand) and Dr H. B. Roberts (Sydney, Australia) for kindly supplying plant materials.     

Anthraquinone pigments from a conidiating mutant ofTrichoderma viride

Summary Two pigments responsible for the yellow-orange color of a brown conidiating mutant of the deuteromyceteTrichoderma viride were isolated and spectroscopically identified as 1,3,6,8-tetrahydroxyanthraquinone (I) and 1-acetyl-2,4,5,7-tetrahydroxy-9,10-anthracenedione (II). Both compounds are known substances but were not yet reported as metabolites of this fungal species. Their relationship to other anthraquinones produced byT. viride is discussed.Dedicated to Dr Z. Vanek, on the occasion of his 60th birthday.Upper case letters denote multiplicity arising from the directly bonded protons, lower case letters that from the geminal and vicinal couplings.     

Two derivatives of farnesylacetone from the brown algaCystophora moniliformis

Summary Farnesylacetone epoxide (3) and the isomeric diketone (4) have been isolated from the brown algaCystophora moniliformis.Acknowledgment. We thank Dr K. Noack for CD measurements and interpretations and Mr K. Harada for algal identification.     

Furospongolide,a new C21 furanoterpene from a marine organism

Summary The structure of a new linear C₂₁ furanoterpene, furospongolide (1), obtained from the marine spongeDysidea herbacea, was determined by spectral means.We thank Professor J. Vacelet for the identification and Dr Loya and Mr Benayahu for the collection of the sponge.     

Two new kaempferol 3,7-diglycosides and kaempferitrin in the fernAsplenium trichomanes

Summary The fronds of the fernAsplenium trichomanes contain kaempferol 3,7-dirhamnoside (1) and the new compounds kaempferol 3-O-a-rhamnoside-7-O-a-arabinoside (2) and kaempferol 3-O-a-arabinoside-7-O-a-rhamnoside (3). The presence of the above flavonoids has been shown by spectroscopic methods and chemical degradations.Acknowledgments. The author thanks Prof. H. Wagner (Institut für pharmazeutische Arzneimittellehre der Universität München, München) for a sample of kaempferol 3,7-dirhamnoside, Dr K. R. Markham (Chemistry Division, D.S.I.R., Petone, New Zealand) for a gift of pectinase and Mr A. D'Urso (Botanic Institute, University of Catania) for help in acquiring the plant material.     

Furodendin,a C22 degraded terpene from the spongePhyllospongia dendyi

Summary The structure of furodendin (5), a minor secondary metabolite of the spongePhyllospongia dendyi, has been solved by spectral methods. Furodendin is probably derived, biosynthetically, by elimination of a C₃ unit from a C₂₅ geranyl-farnesol precursor.Acknowledgment. We thank Dr C. Evans for sponge identification, RRIMP Museum number FN 1516/000.     

Desacetylscalaradial,a cytotoxic metabolite from the spongeCacospongia scalaris

Summary From the marine spongeCacospongia scalaris, scalaradial1, desacetylscalaradial2, and heteronemin3 were isolated. Compound2 showed potent cell growth inhibition. The stereochemistry of3 is briefly discussed.Acknowledgments. The authors are grateful to Prof. T. Hase and Mr R. Nakai for collecting the sponge and to Dr s. Tanida for the sponge identification.     

Antimicrobial activity of carbazole derivatives

Summary Glycozoline and girinimbine isomers (IV andVII) were synthesized and their activity against 2 bacterial strains, viz.E. coli andS. aureus, and 2 fungal strains, viz.C. albicans andA. niger were studied. The hydroxy synthons (III) were also tested. The authors are thankful to Dr B.N. Apte, Association of Microbiologists of India, Bombay Unit, for providing some of the organisms, to Prof. A.K. De, Indian Institute of Technology, for financial assistance, to Prof. G. D. Shah, Department of Chemistry, Indian Institute of Technology for guidance, encouragement and helpful discussions.     

Cocarcinogens of the diterpene ester type fromCroton flavens L. and esophageal cancer in Curaçao

Summary From the roots ofCroton flavens L., 3 highly irritant and tumor promoting Croton factorsF ₁–F ₃ and the corresponding 3 cryptic Croton factorsF₁–F₃ were isolated and characterized as novel esters of 16-hydroxy- and 4-deoxy-16-hydroxyphorbol, respectively. These findings suggest that tumor promoters of the phorbol ester type, ingested through the widespread and frequent use ofCroton flavens according to local habits, may be causally related to the well recognized high rate of esophageal cancer on Curaçao.Dedicated to Prof. Dr H. P. Rusch, Director Wisconsin Clinical Cancer Center, Madison, Wis. USA, on occasion of his 70th birthday. We wish to thank Dr J.F. Morton, Morton Collectanea, University of Miami, Florida, USA, for kindly supplying us with the plant material.     

Identification of (3R,4R)-gD 1(6) as an isolation artefact of cannabinoid acids formed by callus cultures ofCannabis sativa L

Summary For the first time we have isolated a major psychoactive cannabinoid, (3R, 4R)- ¹⁽⁶⁾-tetrahydrocannabinol3 from callus cultures ofCannabis sativa L.3 was obtained as an artefact of the actually formed (3R, 4R)- ¹-tetrahydrocannabinol-3- and/or 5-carboxylic acids1 and2 by subjecting the culture material to a decarboxylation step prior to extraction. No attempt was made to isolated acids1 and2. The identity of3 was confirmed by comparison with an authentic sample of (3R, 4R)- ¹-tetrahydrocannabinol. Culture conditions, isolation procedure and identification of the cannabinoid are described.Acknowledgment. The authors are greatly indebted to Dr W. Heller and Dr G. Schroeder-Frey for deriving the callus cultures from seedlings ofC. sativa and to Prof. N. Amrhein for valuable gifts of culture media and growth regulators.     

Luffariellolide,an anti-inflammatory sesterterpene from the marine spongeLuffariella sp.

Summary Luffariellolide (2) is a sesterterpene from the Palauan spongeLuffariella sp. that has useful anti-inflammatory properties. In contrast with the irreversible action of manoalide (1) on phospholipase A₂, luffariellolide (2) is a slightly less potent but partially reversible PLA₂ inhibitor.30 December 1986Acknowledgment We thank Edward Luedtke, Elise Clason and Ellen Snideman for performing some of the assays reported above. The sponge was identified by Dr. Klaus Rützler, Smithsonian Institution, Washington, D.C. The research was supported by grants from Allergan Pharmaceuticals and the California Sea Grant College Program (Projects R/MP-30 and R/MP-31).     

New aromatic esters of the liverwort,Trichocolea tomentella

Summary 4 new aromatic esters containing isoprene units have been isolated from the liverwort,Trichocolea tomentella, and their structures have been established to be1, 2, 3 and4.The authors are indebted to Professor G. Ourisson of Université Louis Pasteur de Strasbourg, France, and Dr S. Hattori of the Hattori Botanical Laboratory for their helpful suggestion to this work.     

Antimicrobial metabolites of the marine spongeAxinella polycapella

Summary Extracts of the marine spongeAxinella polycapella contain 1,2,4-trihydroxybenzene (1) and 2,2,4,4,5,5-hexahydroxybiphenyl (3) as antimicrobial constituents. Methods of synthesizing3 by, oxidative dimerization of1 were examined.Acknowledgment. We are grateful to Dr Klaus Reutzler for identifying the sponge and one of us (SW) is pleased to acknowledge fellowship support (1-F32-AI_05883-02) from the Public Health Service.     

The absolute configuration of SU 23397: A novel neuroleptic agent

Summary The absolute configuration of a novel chiral neuroleptic agent SU 23397 (I) was determined by ORD comparison of (+)-5-methoxy dihydro coumarilic acid (VIII), a synthetic precursor of SU 23397 (I), with (+)-dihydro coumarilic acid, whose absolute configuration is known⁹. This assignment was confirmed by oxidative degradation of (+)-5-methoxy dihydro coumarilic acidVIII tod-(+)-malic acid.Acknowledgments. We wish to acknowledge and thank Dr J. Karliner, Ciba-Geigy Corporation, Ardsley, New York, for the ORD curves. We thank Dr Max Wilhelm for support and encouragement.     

Preparation of optically pure juvenile hormone I labelled in the ester methyl group with tritium at very high specific activity

Summary Radiolabelled juvenile hormone I (3) was prepared in an optically pure form by an enzymatic method using the capacity of accessory sex gland homogenates from maleHyalophora cecropia to transfer the methyl group of S-adenosyl-L-methionine to the carboxylic acid function of the (10R, 11S)-enantiomer of racemic presursor2; the specific activity of3 is higher than 53 Ci/mmole (1.96 TBq/mmole).We are indebted to Dr W. Thelfer, Philadelphia, for providing us with diapausing pupae of male Cecropia silk moths, and to Dipl.-Biol. G. Klages, Darmstadt, for preparing racemic JH-Iacid. Financial support by the Deutsche Forschungsgemeinschaft (grant No. Em 14/8) is gratefully acknowledged.     

Constituents of propolis

Summary The major constituents of propolis collected in Western Australia have been isolated and identified as pterostilbene (5), xanthorrhoeol (6), sakuranetin (2) and pinostrobin (1).Acknowledgments. We gratefully acknowledge Dr H. Duewell of the University of Newcastle, New South Wales, for an authentic sample of xanthorrhoeol.     

Insect antifeedant terpenes,hot-tasting to humans

Summary Four dialdehyde sesquiterpenoids (1–4) isolated from East AfricanWarburgia plants exhibit powerful antifeeding activity for larvae of the armyworms,Spodoptera exempta andS. littoralis. The hotness of these sesquiterpenes is associated with this activity. The specific absolute stereochemistry of these antifeedants appears to govern the hotness of the taste.The authors are grateful to Proff. K. Nakanishi, A.S. Kende and T. Kubota for their interest and valuable discussion. Succulatal was provided by Dr. Y. Asakawa. This work was initiated during the stay of I.K. at the International Center of Insect Physiology and Ecology, Nairobi, Kenya. We also thank Mr A. Chapya for technical assistance.     

Revised structures for iselin and iliensin and the identity of the former with archangelin

Summary Structures of iselin and iliensin have been revised. The structure (Ib) is secured for iselin by a direct comparison (m.p., UV, IR, PMR) with archangelin. The synthesis of iliensin (IIb) has been effected through the condensation of xanthotoxol (II, R=OH) and -cyclolavandulyl bromide (III). The synthetic product has been shown to be identical with natural iliensin.We thank Dr S.Z. Qasim and Dr M.S. Chadha for the spectral data and C.S.I.R. for a research fellowship to J.V.