The present communication reports the isolation and identification of three lignans from metanolic root extracts of Strychnos guianensis (Aublet) Mart.: olivil (1), cycloolivil (2) and the unknown derivative cycloolivil carbonate (3). From hexane extracts was identified a long chain fatty acid mixture and the triterpene lupeol. The analyses were based on chromatographic and spectroscopy techniques (IR, MS, GC/MS, ¹H-NMR and 13C-NMR, 1D (BB, DEPT 135) and 2D (¹H, ¹ H-COSY, ¹H, 13C-COSY, ¹H, 13C-COSY-LR, HMQC, HMBC and NOESY) and comparison with literature data.

Laboratory-reared Lutzomyia longipalpis (Lutz and Neiva 1912) was tested with extracts of two ichthyotoxic plants, known as timbós, used as fishing poison in the Amazon. Phlebotomines, L. longipalpis, and plants, Antonia ovata and Derris amazonica, were collected in the Raposa-Serra do Sol Indian Reserve, a focus of visceral leishmaniasis in the State of Roraima, Brazil. Extracts were prepared from dried leaves of A. ovata and roots of D. amazonica that were percolated in water, filtered and dried out at 50°C. The solid extract obtained was diluted in water at 150, 200 and 250 mg/ml. The solution was blotted in filter paper placed at the bottom of cylindric glass tubes containing sand flies. For each plant extract and dilution, two series of triplicates with 5 male and 5 female specimens of L. longipalpis were used. Mortality was recorded every 2 h during 72 h of exposure. At 72 h the mortality was as high as 80% for extracts of A. ovata (LD50 = 233 mg/ ml), and 100% for D. amazonica (LD50 = 212 mg/ ml) whereas in the control groups maximum mortality never surpassed 13%. Preliminary assays indicated that A. ovata and D. amazonica displayed significant insecticide effect against L. longipalpis.

Gustavia augusta is used in the folk medicine against leishmaniosis and showed anti-inflammatory action. The phytochemical studies of the plant stem bark have led to the isolation of (22E)-stigmasta-7,22-dien-3beta-ol, 24alpha(S)-ethyl-5alpha-colesta-7,trans-22-dien-3-one, D-friedoolean-14-en-3beta-ol, D-friedoolean-14-en-3-one and D-friedoolean-14-en-3alpha-ol along with stigmasterol, alpha-amyrin, beta-amyrin, lupeol, 3alpha-hidroxi-lupeol and betulinic acid. The structures of these compounds were identified by IR, GC/MS, ¹H and 13C NMR spectral analysis and comparison with literature data.

Dos extratos benzênico e clorofórmico da madeira de Swartzia brachyrachisHarms var. brachyrachis foram isolados, por métodos cromatográficos, uma isoflavona inédita (7,4'—diidroxi -5,3'5'-trimetoxi-6-metilisoflavona), denominada brachyrachisina, c um glicosídio (3-O-β-D-glicopiranosilsitosterol). As estruturas foram elucidadas através de análises espectroscópicas.

From the wood benzene and chloroform extracts of Swartzia brachyrachis Harms var.brachyrachis were isolated, by chromatografph methods, an undocumented isoflavone (7,4'-dihydroxy-5,3',5'—trimethoxy-6-methylisoflavone) named brachyrachisine and a glucoside (3-O-β-D-glucopyranosylsitosterol). The structures were elucidated by spectroscopic analysis.

Resumo Dos extratos metanólicos da casca e do lenho da raíz da Tabernaemontana heterophylla Vahl. (Apocynaceae) foram isolados, além de sitosterol, lupeol e 3—O—acetil—lupeol, seis alcalóides indólicos: coronaridina, vobasina, affinisina, olivacina, voacangina e epiheyneanina.

SUMMARY Six indole alkaloids (coronaridine, voacangine, epiheyneanine, vobasine, affinisine and olivacine) as well as lupeol, 3—0— acetyllupeol and sitosterol were isolated from the roots of Tabernaemontana heterophylla Vahl.

Summary From a drink widely utilized by the Indian nations of western Amazonia, hallucinogenic, two β-carbolinic alkaloids have been isolated.