Cryptoporic and isocryptoporic acids from the fungal cultures of Polyporus arcularius and P. ciliatus
In a chemical study of several fungal cultures of Polyporus, a methyl ester of cryptoporic H was isolated from P. ciliatus, together with cryptoporic acid H and 5-hydroxymethylfuran-3-carboxylic acid. Furthermore, two additional compounds, named isocryptoporic acids H and I, were isolated from P. ar...
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2002
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003 | AR-BaUEN | ||
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024 | 7 | |2 scopus |a 2-s2.0-0036725438 | |
024 | 7 | |2 cas |a Sesquiterpenes | |
030 | |a PYTCA | ||
040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
100 | 1 | |a Cabrera, G.M. | |
245 | 1 | 0 | |a Cryptoporic and isocryptoporic acids from the fungal cultures of Polyporus arcularius and P. ciliatus |
260 | |c 2002 | ||
270 | 1 | 0 | |m Cabrera, G.M.; Depto. de Quimica Organica, Fac. de Ciencias Exactas/Naturales, Universidad de Buenos Aires, Ciudad Universitaria, (1428) Buenos Aires, Argentina; email: gabyc@qo.fcen.uba.ar |
504 | |a Ali, N.A.A., Jansen, R., Pilgrim, H., Liberra, K., Lindequist, U., Hispolon, a yellow pigment from Inonotus hispidus (1996) Phytochemistry, 41, p. 927 | ||
504 | |a Asakawa, Y., Hashimoto, T., Mizuno, Y., Tori, M., Fukazawa, Y., Cryptoporic acids A-G, drimane-type sesquiterpenoids from the fungus Cryptoporus volvatus (1992) Phytochemistry, 31, p. 579 | ||
504 | |a Birkinshaw, J.H., Morgan, E.N., Findlay, W.P.K., Biochemistry of the wood-rotting fungi. Metabolic products of Polyporus benzoinus (1952) Biochem. J., 50, p. 509 | ||
504 | |a Borges da Silveira, R.M., (2001) Contribution to the Knowledge of the Genus Polyporus s. str. (Basidiomycetes) in the Southern Cone of America on the Basis of Morphological, Biological and Molecular Characters, , PhD thesis, Universidad de Buenos Aires | ||
504 | |a Cabrera, G.M., Seldes, A.M., Citrinin derivatives from an intertidal marine Penicillium (1997) Ann. Asoc. Quím. Arg., 85, p. 193 | ||
504 | |a Cavill, G.W.K., Ralph, B.J., Tetaz, J.R., Werner, R.L., The chemistry of mould metabolites. Part I. Isolation and characterization of a red pigment from Coriolus sanguineus (1953) J. Chem. Soc., p. 525 | ||
504 | |a De Bernardi, M., Mellerio, G., Vidari, G., Vita-Finzi, P., Fronza, G., Fungal metabolites. Part 5. Uvidins, new drimane sesquiterpenes from Lactarius uvidus Fries (1980) J. Chem. Soc. Perkin Transactions, 1, p. 221 | ||
504 | |a Fleck, W.F., Schlegel, B., Hoffman, P., Ritzau, M., Heinze, S., Gräfe, U., Isolation of isodrimenediol, a possible intermediate of drimane biosynthesis from Polyporus arcularius (1996) J. Nat. Prod., 59, p. 780 | ||
504 | |a Garlaschelli, L., Mellerio, G., Vidari, G., Vita-Finzi, P., New fatty acid esters of drimane sesquiterpenes from Lactarius uvidus (1994) J. Nat. Prod., 57, p. 905 | ||
504 | |a Gill, M., Steglich, W., Pigments of fungi (1987) Progress in the Chemistry of Organic Natural Products, 51, pp. 1-317. , Herz, W., Grisebach, H., Kirby, G.W., Tamm, C. (Eds.). Springer Publ., Wien, New York | ||
504 | |a Hashimoto, T., Tori, M., Mizuno, Y., Asakawa, Y., Cryptoporic acids A and B, novel bitter drimane sesquiterpenoid ethers of isocitric acid, from the fungus Cryptoporus volvatus (1987) Tetrahedron Letters, 28, p. 6303 | ||
504 | |a Hashimoto, T., Tori, M., Mizuno, Y., Asakawa, Y., Fukasawa, Y., Superoxide release inhibitors, cryptoporic acids C, D and E; dimeric drimane sesquiterpenoid ethers of isocitric acids from the fungus Cryptoporux volvatus (1989) J. Chem. Soc. Chem. Comm., p. 258 | ||
504 | |a Hirotani, M., Furuya, T., Shiro, M., Cryptoporic acids H and I, drimane sesquiterpenes from Ganoderma neo-japonicum and Cryptoporus volvatus (1991) Phytochemistry, 30, p. 1555 | ||
504 | |a Levy, L.M., Cabrera, G.M., Wright, J.E., Seldes, A.M., Indole alkaloids from a culture of the fungus Aporpium caryae (2000) Phytochemistry, 54, p. 941 | ||
504 | |a Morita, Y., Hayashi, Y., Sumi, Y., Kodaira, A., Shibata, H., Haploporic Acid A, a novel dimeric drimane sesquiterpenoid from the basidiomycete Haploporus odorus (1995) Biosci. Biotech. Biochem., 59, p. 2008 | ||
504 | |a Nozoe, S., Agatsuma, T., Takahashi, A., Ohishi, H., In, Y., Kusano, G., Roseolide A, a novel dimeric drimane sesquiterpenoid from the basidiomycete Roseoformes subflexibilis (1993) Tetrahedron Letters, 34, p. 2497 | ||
504 | |a Pevzner, L.M., Ignat'ev, V.M., Ionin, B.I., Synthesis of isomeric phosphonomethylated N, N-diethylfurancarboxamides (1999) Russ. J. Gen. Chem., 69, p. 551 | ||
504 | |a Tai, T., Shingu, T., Kikuchi, T., Tezuka, Y., Akahori, A., Triterpenes from the surface layer of Poria cocos (1995) Phytochemistry, 39, p. 1165 | ||
504 | |a Tori, M., Hamada, N., Sono, M., Sono, Y., Ishikawa, M., Nakashima, K., Hashimoto, T., Asakawa, Y., Synthesis of cryptoporic acid A methyl ester (2000) Tetrahedron Letters, 41, p. 3099 | ||
506 | |2 openaire |e Política editorial | ||
520 | 3 | |a In a chemical study of several fungal cultures of Polyporus, a methyl ester of cryptoporic H was isolated from P. ciliatus, together with cryptoporic acid H and 5-hydroxymethylfuran-3-carboxylic acid. Furthermore, two additional compounds, named isocryptoporic acids H and I, were isolated from P. arcularius. These isocryptoporic acids are isomers of the cryptoporic acids with drimenol instead of albicanol as the terpenoid fragment; their structural elucidation was determined by application of spectroscopic methods. © 2002 Elsevier Science Ltd. All rights reserved. |l eng | |
536 | |a Detalles de la financiación: Universidad de Buenos Aires | ||
536 | |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica | ||
536 | |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas | ||
536 | |a Detalles de la financiación: We thank Dr. Jorge A. Palermo, LANAIS-NMR (CONICET-FCEN, UBA) and Lic. Ivo Hardmeier and INTI for the NMR spectra, LANAIS-EMAR (CONICET-FCEN, UBA) and Washington University Resource for Biomedical and Bio-organic Mass Spectrometry for the mass spectra, UMYMFOR (CONICET-FCEN, UBA), CONICET, ANPCYT and Universidad de Buenos Aires for partial financial support. | ||
593 | |a Depto de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, (1428) Buenos Aires, Argentina | ||
593 | |a Depto de Biología and PRHIDEB-CONICET, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, (1428) Buenos Aires, Argentina | ||
690 | 1 | 0 | |a BASIDIOMYCETE |
690 | 1 | 0 | |a DRIMANE SESQUITERPENOIDS |
690 | 1 | 0 | |a POLYPORALES |
690 | 1 | 0 | |a POLYPORUS |
690 | 1 | 0 | |a 5 HYDROXYMETHYLFURAN 3 CARBOXYLIC ACID |
690 | 1 | 0 | |a ALBICANOL |
690 | 1 | 0 | |a ANTIBIOTIC AGENT |
690 | 1 | 0 | |a CRYPTOPORIC ACID H |
690 | 1 | 0 | |a CRYPTOPORIC ACID H METHYL ESTER |
690 | 1 | 0 | |a DRIMENOL |
690 | 1 | 0 | |a IMMUNOMODULATING AGENT |
690 | 1 | 0 | |a ISOCRYPTOPORIC ACID H |
690 | 1 | 0 | |a ISOCRYPTOPORIC ACID I |
690 | 1 | 0 | |a SESQUITERPENE |
690 | 1 | 0 | |a SESQUITERPENE DERIVATIVE |
690 | 1 | 0 | |a TERPENOID |
690 | 1 | 0 | |a UNCLASSIFIED DRUG |
690 | 1 | 0 | |a SESQUITERPENE |
690 | 1 | 0 | |a ARTICLE |
690 | 1 | 0 | |a BASIDIOMYCETES |
690 | 1 | 0 | |a CHEMICAL STRUCTURE |
690 | 1 | 0 | |a CHEMISTRY |
690 | 1 | 0 | |a CONTROLLED STUDY |
690 | 1 | 0 | |a DRUG ANALYSIS |
690 | 1 | 0 | |a DRUG ISOLATION |
690 | 1 | 0 | |a DRUG STRUCTURE |
690 | 1 | 0 | |a FERMENTATION |
690 | 1 | 0 | |a FUNGAL METABOLISM |
690 | 1 | 0 | |a FUNGUS |
690 | 1 | 0 | |a FUNGUS CULTURE |
690 | 1 | 0 | |a INFRARED SPECTROSCOPY |
690 | 1 | 0 | |a ISOLATION AND PURIFICATION |
690 | 1 | 0 | |a MICROBIOLOGICAL EXAMINATION |
690 | 1 | 0 | |a NONHUMAN |
690 | 1 | 0 | |a NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
690 | 1 | 0 | |a POLYPORUS ARCULARIUS |
690 | 1 | 0 | |a POLYPORUS CILIATUS |
690 | 1 | 0 | |a SPECTROSCOPY |
690 | 1 | 0 | |a STRUCTURE ANALYSIS |
690 | 1 | 0 | |a FUNGUS |
690 | 1 | 0 | |a FERMENTATION |
690 | 1 | 0 | |a FUNGI |
690 | 1 | 0 | |a MAGNETIC RESONANCE SPECTROSCOPY |
690 | 1 | 0 | |a MICROBIAL SENSITIVITY TESTS |
690 | 1 | 0 | |a MOLECULAR STRUCTURE |
690 | 1 | 0 | |a SESQUITERPENES |
690 | 1 | 0 | |a SPECTROSCOPY, FOURIER TRANSFORM INFRARED |
690 | 1 | 0 | |a SUPPORT, NON-U.S. GOV'T |
690 | 1 | 0 | |a FERMENTATION |
690 | 1 | 0 | |a MAGNETIC RESONANCE SPECTROSCOPY |
690 | 1 | 0 | |a MICROBIAL SENSITIVITY TESTS |
690 | 1 | 0 | |a MOLECULAR STRUCTURE |
690 | 1 | 0 | |a SPECTROSCOPY, FOURIER TRANSFORM INFRARED |
690 | 1 | 0 | |a APHYLLOPHORALES |
690 | 1 | 0 | |a POLYPORUS |
690 | 1 | 0 | |a POLYPORUS ARCULARIUS |
690 | 1 | 0 | |a POLYPORUS CILIATUS |
700 | 1 | |a Roberti, M.Julia | |
700 | 1 | |a Wright, J.E. | |
700 | 1 | |a Seldes, A.M. | |
773 | 0 | |d 2002 |g v. 61 |h pp. 189-193 |k n. 2 |p Phytochemistry |x 00319422 |w (AR-BaUEN)CENRE-88 |t Phytochemistry | |
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963 | |a VARI |