226 methanol and water extracts representing 74 mainly native plant species found in Amazonas State, Brazil, were tested at a standard concentration of 500 μg/mL for lethality towards larvae of the brine shrimp species Artemia franciscana.

Ethanol, methanol and water extracts representing mostly native plant species found in the Amazon region were prepared, respectively, by maceration, continuous liquid-solid extraction and infusion, followed by evaporation and freeze-drying. The freeze-dried extracts were tested for lethality toward Aedes aegypti larvae at test concentrations of 500 µg / mL. In general, methanol extracts exhibited the greatest larvicidal activity. The following 7 methanol extracts of (the parts of) the indicated plant species were the most active, resulting in 100 % mortality in A. aegypti larvae: Tapura amazonica Poepp. KEY WORDS

RESUMOParahancornia amapa (Apocynaceae) é típica da região amazônica e conhecida popularmente como amapazeiro e muito utilizada na medicina popular da região Amazônica. O objetivo desse trabalho foi o estudo fitoquímico dos galhos e cascas dessa espécie. Do extrato diclorometânico dos galhos foram isolados o β-sitosterol, estigmasterol, além de triterpenóides pentacíclicos, α-amirina, β-amirina, lupeol e friedelina. Do extrato metanólico das cascas foi isolado o alcaloide indólico isositsiriquina. As estruturas desses compostos foram identificadas por análise dos espectros de massa de alta resolução, Ressonância Magnética Nuclear de 1 H e 13 C e comparações com dados da literatura. Esse é o primeiro relato de isolamento de alcaloide neste gênero. PALAVRAS-CHAVE: Triterpenos, alcaloide, esteroides. Chemical constituents isolated from twigs and barks of amapazeiro (Parahancornia amapa, Apocynaceae)ABSTRACT Parahancornia amapa (Apocynaceae) is typical of the Amazon region and popularly known as amapazeiro and widely used in folk medicine in the Amazon region. The objective of this work was to study the phytochemical composition of twigs and barks of this species. From the dichloromethane extract of twigs were isolated β-sitosterol, stigmasterol, and pentacyclic triterpenoids α-amyrin, β-amyrin, lupeol and friedelin. From the methanol extract of barks was isolated indole alkaloid isositsiriquina. The structures of these compounds were identified by analysis of the mass spectra high-resolution, 1 H and 13 C NMR and comparisons with literature data. This is the first report of isolation of alkaloid in this genus.

Tabebuia incana A.H. Gentry (Bignoniaceae) is a tree from the Brazilian Amazon having medicinal uses and is one several Tabebuia spp. known as pau d'arco or palo de arco in this region. Fractionation of the bark ethanolic extract afforded a mixture of 5 and 8-hydroxy-2-(1-hydroxyethyl)naphtho [2,3-b]furan-4,9-diones (1 and 2, respectively) identified on the basis of nuclear magnetic resonance (NMR), infrared (IR) and mass (MS) spectra, whose in vitro antimalarial and antitumor activity have been shown previously. This is the first study on T. incana bark, and 2 are described in this species for the first time. Also, high performance liquid chromatography (HPLC) analysis of T. incana bark tea revealed the presence of the 1 + 2 mixture peak corresponding to a concentration in the range 10 -6 -10 -5 M. The chromatograms of teas prepared from commercial pau d´arco and T. incana bark were also studied and the presence of the 1 + 2 peak has potential for quality control of commercial plant materials. Diidroxifuranonaftoquinonas bioativas das cascas de Tabebuia incanaA.H. Gentry (Bignoniaceae) e análise por CLAE de infusões de cascas de pau d´arco comercial e T. incana certificada RESUMO Tabebuia incana A.H. Gentry (Bignoniaceae) é uma árvore da Amazônia brasileira com usos medicinais. É uma de várias espécies de Tabebuia conhecidas como pau d'arco ou palo de arco nesta região. O fracionamento do extrato etanólico das cascas resultou no isolamento da mistura de 5 e 8-hidróxi-2-(1-hidroxietil)nafto[2,3-b]furano-4,9-dionas (1 e 2, respectivamente), identificadas com base em seus espectros de ressonância magnética nuclear (RMN), infravermelho (IV) e massa (EM), e cujas atividades antimalárica e antitumoral

LIMONOIDS ISOLATED FROM FRUITS OF Carapa guianensis Aublet (Meliaceae). Six limonoids were isolated in hexane extract obtained from the seeds and pericarps of Carapa guianensis. The structures of the limonoids were determined based on the analysis of High Resolution Mass Spectroscopy and Nuclear Magnetic Resonance (uni-and bi-dimensional experiments) data. This is the first report of isolation of the limonoid 6α-acetoxy-7-deacetilgedunin from the seeds of the C. guianensis species. The limonoid 6-hydroxy-methyl angolensate was also described for the first time in this species.