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Registros recuperados : 7 | |
1. | | LEE, F.N.; DILDAY, R.H.; MOLDENHAUER, K.A.K.; RUTGER, J.N.; YAN, W. Sheath blight and rice blast resistance in recently introduced rice germplasm. ln: Norman, R.J.; Johnston, T.H., (eds.). B.R. Wells rice research studies 1998. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 1999. p. 195-210 (AAES Research Series ; 468)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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2. | | MOLDENHAUER, K.A.K.; GIBBONS, J.W.; LEE, F.N.; NORMAN, R.J.; BERNHARDT, J.L.; DILDAY, R.H.; RUTGER, J.N.; BLOCKER, M.M.; TOLBERT, A.C. Breeding and evaluation for improved rice varieties- The Arkansas rice breeding and development program. ln: Norman, R.J.; Johnston, T.H., (eds.). B.R. Wells rice research studies 1998. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 1999. p. 20-27 (AAES Research Series ; 468)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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3. | | MOLDENHAUER, K.A.K.; GIBBONS, J.W.; LEE, F.N.; NORMAN, R.J.; BERNHARDT, J.L.; ANDERS, M.A.; DILDAY, R.H.; RUTGER, J.N.; BLOCKER, M.M.; TOLBERT, A.C. Breeding and evaluation for improved rice cultivar. The Arkansas rice-breeding and development program. ln: Norman, R.J.; Beyrouty, C.A. B.R. Wells Rice research studies 1999. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 2000. p. 36-45 (AAES Research Series ; 476)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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4. | | MOLDENHAUER, K.A.K.; GIBBONS, J.W.; LEE, F.N.; NORMAN, R.J.; BERNHARDT, J.L.; ANDERS, M.A.; WILSON, C.E.; SLATON, N.A.; RUTGER, J.N.; TAI, T.; BRYANT, R.; BLOCKER, M.M.; TOLBERT, A.C. Breeding and evaluation for improved rice varieties: the Arkansas rice breeding and development program. ln: Norman, R.J.; Meullenet, J.F. B.R. Wells Rice research studies 2000. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 2001. p. 20-26 (AAES Research Series ; 485)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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5. | | GIBBONS, J.W.; MOLDENHAUER, K.A.K.; LEE, F.N.; BERNHARDT, J.L.; ANDERS, M.; SLATON, N.A.; NORMAN, R.J.; WILSON, C.E.; DILDAY, R.H.; RUTGER, J.N.; BULLOCH, J.M.; BLOCKER, M.M.; TOLBERT, C.A. Development of semi-dwarf long and medium grain cultivars. ln: Norman, R.J.; Meullenet, J.F. B.R. Wells Rice research studies 2000. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 2001. p. 13-19 (AAES Research Series ; 485)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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6. | | BLANCO, P.H.; SUÁREZ, E.; DEUS, J.E.; RAMÍREZ, J.; NAVARRO, W.; FARACOM, A.A.; BASTOS, C.R.; EIZENGA, G.C.; BOLLICH, C.N.; RUTGER, J.N.; MALUSZYNSKI, M. Multi-location yield of rice mutant in the Latin American Region: abstract. ln: Rice Technical Working Group, 28., 2000 Proceedings. Biloxi, Mississippi (USA): Rice Technical Working Group, 2000. p. 38-39.Biblioteca(s): INIA Treinta y Tres. |
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7. | | GIBBONS, J.W.; MOLDENHAUER, K.A.K.; LEE, F.N.; BERNHARDT, J.L.; ANDERS, M.; SLATON, N.A.; NORMAN, R.J.; DILDAY, R.H.; RUTGER, J.N.; BLOCKER, M.M.; BULLOCH, J.M.; TOLBERT, A.C. Rice breeding and genetics: Development of semi-dwarf long and medium-grain cultivars. ln: Norman, R.J.; Beyrouty, C.A. B.R. Wells Rice research studies 1999. Fayetteville, Arkansas (USA): Arkansas Agricultural Experiment Station, 2000. p. 28-35 (AAES Research Series ; 476)Biblioteca(s): INIA Tacuarembó; INIA Treinta y Tres. |
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Registros recuperados : 7 | |
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| Acceso al texto completo restringido a Biblioteca INIA Tacuarembó. Por información adicional contacte bibliotb@tb.inia.org.uy. |
Registro completo
|
Biblioteca (s) : |
INIA Tacuarembó. |
Fecha actual : |
21/02/2014 |
Actualizado : |
02/06/2020 |
Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
Circulación / Nivel : |
Internacional - -- |
Autor : |
REINA, L.; BOTTINI, G.; BENNADJI, Z.; VINCIGUERRA, V.; FERREIRA CHIESA, F.A.; MENÉNDEZ, P.; MOYNA, G. |
Afiliación : |
LUIS REINA, Universidad de la República (UdelaR)/ Facultad de Química.; GUALBERTO BOTTINI, cDepartamento de Química del Litoral, CENUR Litoral Norte, UdelaR, Paysandú, Uruguay.; ZOHRA BENNADJI SOUALHIA, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; VITTORIO VINCIGUERRA, Dipartimento per la Innovazione nei Sistemi Biologici, Agroalimentari e Forestali, Università della Tuscia, Largo dell’Università, Italy; FERNANDO AMAURY FERREIRA CHIESA, Universidad de la República (UdelaR)/ Facultad de Química.; PILAR MENÉNDEZ, Universidad de la República (UdelaR)/ Facultad de Química.; GUILLERMO MOYNA, c Departamento de Química del Litoral, CENUR Litoral Norte, UdelaR, Paysandú, Uruguay. |
Título : |
Aggregation Behavior of 6-Isocassine and N-Methyl-6-Isocassine: Insights into the Biological Mode of Action of Lipid Alkaloids. |
Fecha de publicación : |
2016 |
Fuente / Imprenta : |
Natural Product Communications, 2016, Volume 11, Issue 11, Pages 1641-1644. DOI. https://doi.org/10.1177/1934578X1601101104 |
DOI : |
10.1177/1934578X1601101104 |
Idioma : |
Inglés |
Notas : |
Article history: Received: February 1st, 2016// Accepted: May 25th, 2016. Dedicated to the memory of our esteemed colleague and friend Eduardo Alonso Paz. Acknowledgments - Funding from the INIA (award L4-FO-21-0-00), the ANII (award POS_NAC_2014_1_102226), the DGRC-UdelaR (Programa 720), and the PEDECIBA is greatly acknowledged. |
Contenido : |
The aggregation behavior of 6-isocassine and N-methyl-6-isocassine, two piperidin-3-ol alkaloids isolated respectively from the barks of Prosopis nigra and
P. affinis, was investigated using a combination of NOE experiments and diffusion measurements in solvents of varying polarity and hydrogen bonding
capacity. While the NOE enhancements for N-methyl-6-isocassine are positive, regardless of the solvent, those for 6-isocassine shift from negative to positive
when going from chloroform-d to methanol-d4 solution. In addition, despite the self-diffusion coefficients of both compounds being virtually identical in
methanol-d4, N-methyl-6-isocassine diffuses nearly twice as fast as the non-methylated alkaloid in chloroform-d. The changes in rotational and translational
dynamics observed between solvents for 6-isocassine suggest that the molecule forms dimeric head-to-head aggregates in non-polar aprotic environments, a
behavior that could help explain the biological mode of action that has been proposed for this type of alkaloids. |
Palabras claves : |
AGGREGATION; DIFFUSION; HYDROGEN BONDING; NOE ENHANCEMENTS; PIPERIDINE ALKALOIDS. |
Asunto categoría : |
K10 Producción forestal |
Marc : |
LEADER 02269naa a2200277 a 4500 001 1016936 005 2020-06-02 008 2016 bl uuuu u00u1 u #d 024 7 $a10.1177/1934578X1601101104$2DOI 100 1 $aREINA, L. 245 $aAggregation Behavior of 6-Isocassine and N-Methyl-6-Isocassine$bInsights into the Biological Mode of Action of Lipid Alkaloids.$h[electronic resource] 260 $c2016 500 $aArticle history: Received: February 1st, 2016// Accepted: May 25th, 2016. Dedicated to the memory of our esteemed colleague and friend Eduardo Alonso Paz. Acknowledgments - Funding from the INIA (award L4-FO-21-0-00), the ANII (award POS_NAC_2014_1_102226), the DGRC-UdelaR (Programa 720), and the PEDECIBA is greatly acknowledged. 520 $aThe aggregation behavior of 6-isocassine and N-methyl-6-isocassine, two piperidin-3-ol alkaloids isolated respectively from the barks of Prosopis nigra and P. affinis, was investigated using a combination of NOE experiments and diffusion measurements in solvents of varying polarity and hydrogen bonding capacity. While the NOE enhancements for N-methyl-6-isocassine are positive, regardless of the solvent, those for 6-isocassine shift from negative to positive when going from chloroform-d to methanol-d4 solution. In addition, despite the self-diffusion coefficients of both compounds being virtually identical in methanol-d4, N-methyl-6-isocassine diffuses nearly twice as fast as the non-methylated alkaloid in chloroform-d. The changes in rotational and translational dynamics observed between solvents for 6-isocassine suggest that the molecule forms dimeric head-to-head aggregates in non-polar aprotic environments, a behavior that could help explain the biological mode of action that has been proposed for this type of alkaloids. 653 $aAGGREGATION 653 $aDIFFUSION 653 $aHYDROGEN BONDING 653 $aNOE ENHANCEMENTS 653 $aPIPERIDINE ALKALOIDS 700 1 $aBOTTINI, G. 700 1 $aBENNADJI, Z. 700 1 $aVINCIGUERRA, V. 700 1 $aFERREIRA CHIESA, F.A. 700 1 $aMENÉNDEZ, P. 700 1 $aMOYNA, G. 773 $tNatural Product Communications, 2016, Volume 11, Issue 11, Pages 1641-1644. DOI. https://doi.org/10.1177/1934578X1601101104
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