Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob.
98 páginas : ilustraciones, gráficas
- Autores:
-
Enciso Guzmán, Oscar Eduardo
- Tipo de recurso:
- Trabajo de grado de pregrado
- Fecha de publicación:
- 2013
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- Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
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- Palabra clave:
- Compositae
Metabolitos vegetales
Análisis químico de las plantas
Chromolaena leivensis
Metabolitos vegetales
Chromolaena
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Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| title |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| spellingShingle |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. Compositae Metabolitos vegetales Análisis químico de las plantas Chromolaena leivensis Metabolitos vegetales Chromolaena |
| title_short |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| title_full |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| title_fullStr |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| title_full_unstemmed |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| title_sort |
Metabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob. |
| dc.creator.fl_str_mv |
Enciso Guzmán, Oscar Eduardo |
| dc.contributor.advisor.spa.fl_str_mv |
Rodríguez Aguirre, Oscar Eduardo, dir. Torrenegra Guerrero, Rubén Darío, dir. |
| dc.contributor.author.spa.fl_str_mv |
Enciso Guzmán, Oscar Eduardo |
| dc.subject.lemb.spa.fl_str_mv |
Compositae Metabolitos vegetales Análisis químico de las plantas |
| topic |
Compositae Metabolitos vegetales Análisis químico de las plantas Chromolaena leivensis Metabolitos vegetales Chromolaena |
| dc.subject.proposal.spa.fl_str_mv |
Chromolaena leivensis Metabolitos vegetales |
| dc.subject.agrovoc.spa.fl_str_mv |
Chromolaena |
| description |
98 páginas : ilustraciones, gráficas |
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2013 |
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2013 |
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2019-07-29T20:11:33Z |
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2019-07-29T20:11:33Z |
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Trabajo de grado - Pregrado |
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AHMED, A.A. Whittemore A.T, Mabry, T.J. 1985, A heliangolide from Chromolaena glaberrima - Phytochemistry 24 (3), 605 - 606. ANAYA L, Ana Luisa. Relaciones Químicas entre Organismos: Aspectos básicos y perspectivas de su aplicación. México: Plaza y Valdez S.A., 2004. p. 181-185. BARUA R.N., Sharma R.P. Thyagarajan G. and Werner H, 1978, Flavonoids of Chromolaena odorata, Phytochemistry, 17 (10), 1807-1808 BECERRA P.P., 1992. Estudio fitoquímico de la Chromolaena leivensis y su actividad antibacteriana. Tesis de maestría, Pontificia Universidad Javeriana, Bogotá. BILLER A., Boppre M, Witte L, Hartmann T, 1994. Pyrrolizidine alkaloids in Chromolaena odorata. Chemical and chemoecological aspects, Phytochemistry 35 (3), 615 - 619. BOLLIGER, H., Brenner M., Ganshirt., Mangold H., Seiler H., Stanhl E., and Waldi D. 1965. Thin-Layer Chromatography a laboratory hanbook. Academic press inc, Springer-Verlac , 553 p BOHLMANN F., Zdero C., Fiedler L., Robinson H., and King Robert M. 1981. A labdane derivative from Chromolaena collina and a p-hydroxyacetophenone derivative from Stomatanthes corumbensis. Phytochemistry 20 ( 5 ), 1141 – 1143. BOHLMANN, F., Gupta R., King, K., Robinson, H., M. 1981. Prostaglandin-like fatty acid derivative from Chromolaena morii. Phytochemistry 20 ( 6 ), 1417 - 1418. BOHLMANN F., Singh P., Jakupovic J., King, R.M. and Robinson H. 1982. Three cadinene derivatives and a prostaglandin-like acid from Chromolaena species, Phytochemistry 21 (2), 371 - 374. BOHLMANN F.,Borthakur, King, N. and Robinson H., R.M. 1982. Further prostaglandin-like fatty acids from Chromolaena morii. Phytochemistry 21 (1), 125 – 127. BOUDA, H., Tapondjou L.A., Fontem, D.A. and Gumedzoe M., 2001. Effect of essential oils from leaves of Ageratum conyzoides, Lantana camara and Chromolaena odorata on the mortality of Sitophilus zeamais (Coleoptera, Curculionidae). J. Stored Prod Res. 37 (2), 103-109 CANNEL R., J.P. 1998, Natural Products Isolation. Humana Press, 472 p. CLIMENT M., García H., Iborra S. y Morera I. 2005. Experimentación en Química: Química Orgánica, Ingeniería Química. Editorial Universidad politécnica de Valencia. p.104. CRONQUIST, A. 1981. An integrated system of classification of flowering plants. Columbia University Press, Nueva York. DEANNA M. y Masahisa H., 2002. Fotoquímica Orgánica. Consejo de Desarrollo Científico y Humanistico. Universidad central de Venezuela. Pag 29-31. De GUTIÉRREZ, A.N., Catalán C., A.N., Díaz, J.G., Herz, W. 1995. Sesquiterpene lactones, a labdane and other constituents of Urolepis hecatantha and Chromolaena arnottiana. Phytochemistry 39 (4), 795 - 800. DOMÍNGUEZ, X. 1973. Métodos de Investigación Fitoquímica. 1ª edición.México D.F. Editorial Limusa. P. 39-41, 45, 55. El-SAYED, N.H., MiskI M., Whittemore, A.T. and Mabry, T.J. 1988. Sesquiterpene lactones from Chromolaena opadoclinia. Phytochemistry 27 (10), 3312 – 3314 ESPITIA C., 1992. Química del genero Chromolaena, flavanonas de Chromolaena tyleri. Facultad de Ciencias. Departamento de Química. Universidad Nacional de Colombia. Chromolaena subscandens GUZMÁN, A., Torrenegra, R., Rodríguez, O. 2008. Flavonoides de Chromolaena subscandens (Hieron.) R.M. King & H. Rob. Revista de Productos Naturales, Volumen 2, N°1. GUZMÁN A., A. J. 2007. Fitoquímica de la especie colombiana Chromolaena subscandens (Hieron) R.M. King & H. Rob. Y determinación de su actividad antimicrobiana. Tesis de maestría, Pontificia Universidad Javeriana, Bogotá HARBORNE, J. B. 1973. Phytochemical Methods. Chapman and Hall, 266 p. HARBORNE, J. B., Mabry, T.J. and Mabry, H. 1975. The Flavonoids. Chapman and Hall, p. 866 – 909. HARBORNE, J. B. and Mabry, T.J. 1982. The Flavonoids Advances in Research. Chapman and Hall, 744 p. IROBI, O.N. 1992. Activities of Chromolaena odorata (Compositae) leaf extract against Pseudomonas aeruginosa and Streptococcus faecalis. J. Ethnopharmacol. 37 (1), 81 - 83. KATINAS. L., Gutierrez. D., Grossi. M., Crisci. J. 2007. Panoma de la Familia Asteracea (=compositae). Argent. Bot 42, p. 113 KING, R.M. and Robinson, H. 1970a. Studies in the Eupatorieae (compositae) XXIX the genus Chromolaena. Phytologia, 20 ( 3), 196 – 209. KING, R.M. and Robinson, H. 1970b. Studies in the Eupatorieae (Compositae). XXV. A new genus Eupatoriadelphus. Phytologia 19, 431– 432. MCMASTER, Marvin C. GC/MS: a practical user’s guide. 2 ed. New Jersey: John Willey & Sons Inc., 2008. p. 4-6. PHAN T.T., Hughes, M.A. and Cherry, G.W. 1998. Enhanced proliferation of fibroblasts and endothelial cells treated with an extract of the leaves of Chromolaena odorata (Eupolin), an herbal remedy for treating wounds. Plast Reconstr Surg. 101 (3), 756 - 765. PHAN, T.T., Allen, J., Hughes, M.A, Cherry, G. and Wojnarowska, F. 2000. Upregulation of adhesion complex proteins and fibronectin by human keratinocytes treated with an aqueous extract from the leaves of Chromolaena odorata (Eupolin). Eur J Dermatol. 10 (7), 522. PHAN, T.T., Hughes, M.A. and Cherry, G.W. 2001. Effects of an aqueous extract from the leaves of Chromolaena odorata (Eupolin) on the proliferation of human keratinocytes and on their migration in an in vitro model of reepithelialization. Wound Repair Regen. 9 (4), 305 - 313. RODRÍGUEZ A., TORRENEGRA G., 2005 Flavonoides de Chromolaena tacotana (Klatt) R.M. King y H. Rod. Actualidades Biológicas. Vol. 27. SCHMIDT, G.J. AND Schilling., E.E. 2000. Phylogeny and biogeography of Eupatorium (Asteraceae, Eupatorieae) based on nuclear ITS sequence data. American Journal of Botany 87, 716–726. SKOOG, Douglas; HOLLER, F. James y NIEMAN, Timothy. Principios de Análisis Instrumental. 5 ed. Madrid: Editorial Mc Graw Hill, 2001. p. 568. STEYERMARK. J. and BERRY P. 1997. Flora of the Venezuelan Guyana. Ed. Missiouri Botanical Garden, p. 181-251. TALEB – CONTINI, S.H., Salvador, M.J., Balanco, J.M., Albuquerque, S. and DE Oliveira, D.C. 2004. Antiprotozoal effect of crude extracts and flavonoids isolated from Chromolaena hirsuta (Asteraceae). Phytother Res. 18 (3), 250 - 254. TAMAYO - Castillo, G. Jakupovic, J. Bohlmann, F. King, R. M. Robinson, H. 1989. EntClerodane derivatives from Chromolaena connivens, Phytochemistry 28 ( 2 ), 641 – 642. THANG, P.T., Patrick, S., Teik, L.S. and Yung, C.S. 2001. Anti-oxidant effects of the extracts from the leaves of Chromolaena odorata on human dermal fibroblasts and epidermal keratinocytes against hydrogen peroxide and hypoxanthine-xanthine oxidase induced damage. Burns. 27 (4), 319 - 327. |
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Rodríguez Aguirre, Oscar Eduardo, dir.Torrenegra Guerrero, Rubén Darío, dir.Enciso Guzmán, Oscar Eduardo2019-07-29T20:11:33Z2019-07-29T20:11:33Z2013https://repository.udca.edu.co/handle/11158/1853QI001 E51i 2013 (204539)98 páginas : ilustraciones, gráficasEl estudio se basó en la Identificación de metabolitos secundarios presentes en la raíz de la especie colombiana Chromolaena leivensis (Hieron) King & H. Rob. Para lo cual se realizó un extracto total etanolico en equipo Soxhlet. Dicho extracto fue fraccionado por percolación con solventes de polaridad creciente desde (éter de petróleo, diclorometano y metanol). La fracción éter de petróleo se eluye por cromatografía en columna (CC) con mezclas de polaridad creciente (pretrol, petrol:diclorometano 9:1; 8:2, diclorometano, hasta metanol), las subfracciones menos complejas fueron evaluadas por CG-EM y comparando con las bases de datos Nist-08 y Willey-8. Se identificaron compuestos como: 6,10,14-trimetil-2-pentadecanona, acido-ascórbico-2,6-dihexadecanoato, 1-docosanol, 1-Heptacosanol, friedeoolean-3-ol, 1-pentacosanol, vainillina, 2,2´-isopropilidenedifurano, Cholest-7-en-3-ol, Cholest-4-en-3-ona, Heneicosano, Hexatriacontano, Acido-mono(etil-hexil)-1,2-bencendicarboxilico, Friedelan-3-ona, 1-nonadecanol, tetracosanol, acido-mono(2-etil-hexil)-1,2-bencenedicarboxilico, Friedelanol, 5,7-dihidroxi-flavanonaIncluye bibliografíaPregradoQuímico(a)application/pdfspaBogotá : Universidad de Ciencias Aplicadas y Ambientales, 2013Facultad de CienciasQuímicaDerechos Reservados - Universidad de Ciencias Aplicadas y Ambientaleshttps://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/closedAccessAtribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)http://purl.org/coar/access_right/c_14cbMetabolitos secundarios de raiz de Chromolaena leivensis (Hieron) King y H. Rob.Trabajo de grado - Pregradohttp://purl.org/coar/resource_type/c_7a1finfo:eu-repo/semantics/bachelorThesisinfo:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/TPhttp://purl.org/coar/version/c_970fb48d4fbd8a85CompositaeMetabolitos vegetalesAnálisis químico de las plantasChromolaena leivensisMetabolitos vegetalesChromolaenaAHMED, A.A. Whittemore A.T, Mabry, T.J. 1985, A heliangolide from Chromolaena glaberrima - Phytochemistry 24 (3), 605 - 606.ANAYA L, Ana Luisa. Relaciones Químicas entre Organismos: Aspectos básicos y perspectivas de su aplicación. México: Plaza y Valdez S.A., 2004. p. 181-185.BARUA R.N., Sharma R.P. Thyagarajan G. and Werner H, 1978, Flavonoids of Chromolaena odorata, Phytochemistry, 17 (10), 1807-1808BECERRA P.P., 1992. Estudio fitoquímico de la Chromolaena leivensis y su actividad antibacteriana. Tesis de maestría, Pontificia Universidad Javeriana, Bogotá.BILLER A., Boppre M, Witte L, Hartmann T, 1994. Pyrrolizidine alkaloids in Chromolaena odorata. Chemical and chemoecological aspects, Phytochemistry 35 (3), 615 - 619.BOLLIGER, H., Brenner M., Ganshirt., Mangold H., Seiler H., Stanhl E., and Waldi D. 1965. Thin-Layer Chromatography a laboratory hanbook. Academic press inc, Springer-Verlac , 553 pBOHLMANN F., Zdero C., Fiedler L., Robinson H., and King Robert M. 1981. A labdane derivative from Chromolaena collina and a p-hydroxyacetophenone derivative from Stomatanthes corumbensis. Phytochemistry 20 ( 5 ), 1141 – 1143.BOHLMANN, F., Gupta R., King, K., Robinson, H., M. 1981. Prostaglandin-like fatty acid derivative from Chromolaena morii. Phytochemistry 20 ( 6 ), 1417 - 1418.BOHLMANN F., Singh P., Jakupovic J., King, R.M. and Robinson H. 1982. Three cadinene derivatives and a prostaglandin-like acid from Chromolaena species, Phytochemistry 21 (2), 371 - 374.BOHLMANN F.,Borthakur, King, N. and Robinson H., R.M. 1982. Further prostaglandin-like fatty acids from Chromolaena morii. Phytochemistry 21 (1), 125 – 127.BOUDA, H., Tapondjou L.A., Fontem, D.A. and Gumedzoe M., 2001. Effect of essential oils from leaves of Ageratum conyzoides, Lantana camara and Chromolaena odorata on the mortality of Sitophilus zeamais (Coleoptera, Curculionidae). J. Stored Prod Res. 37 (2), 103-109CANNEL R., J.P. 1998, Natural Products Isolation. Humana Press, 472 p.CLIMENT M., García H., Iborra S. y Morera I. 2005. Experimentación en Química: Química Orgánica, Ingeniería Química. Editorial Universidad politécnica de Valencia. p.104.CRONQUIST, A. 1981. An integrated system of classification of flowering plants. Columbia University Press, Nueva York.DEANNA M. y Masahisa H., 2002. Fotoquímica Orgánica. Consejo de Desarrollo Científico y Humanistico. Universidad central de Venezuela. Pag 29-31.De GUTIÉRREZ, A.N., Catalán C., A.N., Díaz, J.G., Herz, W. 1995. Sesquiterpene lactones, a labdane and other constituents of Urolepis hecatantha and Chromolaena arnottiana. Phytochemistry 39 (4), 795 - 800.DOMÍNGUEZ, X. 1973. Métodos de Investigación Fitoquímica. 1ª edición.México D.F. Editorial Limusa. P. 39-41, 45, 55.El-SAYED, N.H., MiskI M., Whittemore, A.T. and Mabry, T.J. 1988. Sesquiterpene lactones from Chromolaena opadoclinia. Phytochemistry 27 (10), 3312 – 3314ESPITIA C., 1992. Química del genero Chromolaena, flavanonas de Chromolaena tyleri. Facultad de Ciencias. Departamento de Química. Universidad Nacional de Colombia. Chromolaena subscandensGUZMÁN, A., Torrenegra, R., Rodríguez, O. 2008. Flavonoides de Chromolaena subscandens (Hieron.) R.M. King & H. Rob. Revista de Productos Naturales, Volumen 2, N°1.GUZMÁN A., A. J. 2007. Fitoquímica de la especie colombiana Chromolaena subscandens (Hieron) R.M. King & H. Rob. Y determinación de su actividad antimicrobiana. Tesis de maestría, Pontificia Universidad Javeriana, BogotáHARBORNE, J. B. 1973. Phytochemical Methods. Chapman and Hall, 266 p.HARBORNE, J. B., Mabry, T.J. and Mabry, H. 1975. The Flavonoids. Chapman and Hall, p. 866 – 909.HARBORNE, J. B. and Mabry, T.J. 1982. The Flavonoids Advances in Research. Chapman and Hall, 744 p.IROBI, O.N. 1992. Activities of Chromolaena odorata (Compositae) leaf extract against Pseudomonas aeruginosa and Streptococcus faecalis. J. Ethnopharmacol. 37 (1), 81 - 83.KATINAS. L., Gutierrez. D., Grossi. M., Crisci. J. 2007. Panoma de la Familia Asteracea (=compositae). Argent. Bot 42, p. 113KING, R.M. and Robinson, H. 1970a. Studies in the Eupatorieae (compositae) XXIX the genus Chromolaena. Phytologia, 20 ( 3), 196 – 209.KING, R.M. and Robinson, H. 1970b. Studies in the Eupatorieae (Compositae). XXV. A new genus Eupatoriadelphus. Phytologia 19, 431– 432.MCMASTER, Marvin C. GC/MS: a practical user’s guide. 2 ed. New Jersey: John Willey & Sons Inc., 2008. p. 4-6.PHAN T.T., Hughes, M.A. and Cherry, G.W. 1998. Enhanced proliferation of fibroblasts and endothelial cells treated with an extract of the leaves of Chromolaena odorata (Eupolin), an herbal remedy for treating wounds. Plast Reconstr Surg. 101 (3), 756 - 765.PHAN, T.T., Allen, J., Hughes, M.A, Cherry, G. and Wojnarowska, F. 2000. Upregulation of adhesion complex proteins and fibronectin by human keratinocytes treated with an aqueous extract from the leaves of Chromolaena odorata (Eupolin). Eur J Dermatol. 10 (7), 522.PHAN, T.T., Hughes, M.A. and Cherry, G.W. 2001. Effects of an aqueous extract from the leaves of Chromolaena odorata (Eupolin) on the proliferation of human keratinocytes and on their migration in an in vitro model of reepithelialization. Wound Repair Regen. 9 (4), 305 - 313.RODRÍGUEZ A., TORRENEGRA G., 2005 Flavonoides de Chromolaena tacotana (Klatt) R.M. King y H. Rod. Actualidades Biológicas. Vol. 27.SCHMIDT, G.J. AND Schilling., E.E. 2000. Phylogeny and biogeography of Eupatorium (Asteraceae, Eupatorieae) based on nuclear ITS sequence data. American Journal of Botany 87, 716–726.SKOOG, Douglas; HOLLER, F. James y NIEMAN, Timothy. Principios de Análisis Instrumental. 5 ed. Madrid: Editorial Mc Graw Hill, 2001. p. 568.STEYERMARK. J. and BERRY P. 1997. Flora of the Venezuelan Guyana. Ed. Missiouri Botanical Garden, p. 181-251.TALEB – CONTINI, S.H., Salvador, M.J., Balanco, J.M., Albuquerque, S. and DE Oliveira, D.C. 2004. Antiprotozoal effect of crude extracts and flavonoids isolated from Chromolaena hirsuta (Asteraceae). Phytother Res. 18 (3), 250 - 254.TAMAYO - Castillo, G. Jakupovic, J. Bohlmann, F. King, R. M. Robinson, H. 1989. EntClerodane derivatives from Chromolaena connivens, Phytochemistry 28 ( 2 ), 641 – 642.THANG, P.T., Patrick, S., Teik, L.S. and Yung, C.S. 2001. Anti-oxidant effects of the extracts from the leaves of Chromolaena odorata on human dermal fibroblasts and epidermal keratinocytes against hydrogen peroxide and hypoxanthine-xanthine oxidase induced damage. 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en las Obras Colectivas;
b.	Distribuir copias o fonogramas de las Obras, exhibirlas públicamente, ejecutarlas públicamente y/o ponerlas a disposición pública, incluyéndolas como incorporadas en Obras Colectivas, según corresponda;
c.	Distribuir copias de las Obras Derivadas que se generen, exhibirlas públicamente, ejecutarlas públicamente y/o ponerlas a disposición pública.
Los derechos mencionados anteriormente pueden ser ejercidos en todos los medios y formatos, actualmente conocidos o que se inventen en el futuro. Los derechos antes mencionados incluyen el derecho a realizar dichas modificaciones en la medida que sean técnicamente necesarias para ejercer los derechos en otro medio o formatos, pero de otra manera usted no está autorizado para realizar obras derivadas.Todos los derechos no otorgados expresamente por el Licenciante quedan por este medio reservados, incluyendo pero sin limitarse a aquellos que se mencionan en las secciones 4(d) y 4(e).
4. Restricciones.
La licencia otorgada en la anterior Sección 3 está expresamente sujeta y limitada por las siguientes restricciones:
a.	Usted puede distribuir, exhibir públicamente, ejecutar públicamente, o poner a disposición pública la Obra sólo bajo las condiciones de esta Licencia, y Usted debe incluir una copia de esta licencia o del Identificador Universal de Recursos de la misma con cada copia de la Obra que distribuya, exhiba públicamente, ejecute públicamente o ponga a disposición pública. No es posible ofrecer o imponer ninguna condición sobre la Obra que altere o limite las condiciones de esta Licencia o el ejercicio de los derechos de los destinatarios otorgados en este documento. No es posible sublicenciar la Obra. Usted debe mantener intactos todos los avisos que hagan referencia a esta Licencia y a la cláusula de limitación de garantías. Usted no puede distribuir, exhibir públicamente, ejecutar públicamente, o poner a disposición pública la Obra con alguna medida tecnológica que controle el acceso o la utilización de ella de una forma que sea inconsistente con las condiciones de esta Licencia. Lo anterior se aplica a la Obra incorporada a una Obra Colectiva, pero esto no exige que la Obra Colectiva aparte de la obra misma quede sujeta a las condiciones de esta Licencia. Si Usted crea una Obra Colectiva, previo aviso de cualquier Licenciante debe, en la medida de lo posible, eliminar de la Obra Colectiva cualquier referencia a dicho Licenciante o al Autor Original, según lo solicitado por el Licenciante y conforme lo exige la cláusula 4(c).
b.	Usted no puede ejercer ninguno de los derechos que le han sido otorgados en la Sección 3 precedente de modo que estén principalmente destinados o directamente dirigidos a conseguir un provecho comercial o una compensación monetaria privada. El intercambio de la Obra por otras obras protegidas por derechos de autor, ya sea a través de un sistema para compartir archivos digitales (digital file-sharing) o de cualquier otra manera no será considerado como estar destinado principalmente o dirigido directamente a conseguir un provecho comercial o una compensación monetaria privada, siempre que no se realice un pago mediante una compensación monetaria en relación con el intercambio de obras protegidas por el derecho de autor.
c.	Si usted distribuye, exhibe públicamente, ejecuta públicamente o ejecuta públicamente en forma digital la Obra o cualquier Obra Derivada u Obra Colectiva, Usted debe mantener intacta toda la información de derecho de autor de la Obra y proporcionar, de forma razonable según el medio o manera que Usted esté utilizando: (i) el nombre del Autor Original si está provisto (o seudónimo, si fuere aplicable), y/o (ii) el nombre de la parte o las partes que el Autor Original y/o el Licenciante hubieren designado para la atribución (v.g., un instituto patrocinador, editorial, publicación) en la información de los derechos de autor del Licenciante, términos de servicios o de otras formas razonables; el título de la Obra si está provisto; en la medida de lo razonablemente factible y, si está provisto, el Identificador Uniforme de Recursos (Uniform Resource Identifier) que el Licenciante especifica para ser asociado con la Obra, salvo que tal URI no se refiera a la nota sobre los derechos de autor o a la información sobre el licenciamiento de la Obra; y en el caso de una Obra Derivada, atribuir el crédito identificando el uso de la Obra en la Obra Derivada (v.g., "Traducción Francesa de la Obra del Autor Original," o "Guión Cinematográfico basado en la Obra original del Autor Original"). Tal crédito puede ser implementado de cualquier forma razonable; en el caso, sin embargo, de Obras Derivadas u Obras Colectivas, tal crédito aparecerá, como mínimo, donde aparece el crédito de cualquier otro autor comparable y de una manera, al menos, tan destacada como el crédito de otro autor comparable.
d.	Para evitar toda confusión, el Licenciante aclara que, cuando la obra es una composición musical:
i.	Regalías por interpretación y ejecución bajo licencias generales. El Licenciante se reserva el derecho exclusivo de autorizar la ejecución pública o la ejecución pública digital de la obra y de recolectar, sea individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, SAYCO), las regalías por la ejecución pública o por la ejecución pública digital de la obra (por ejemplo Webcast) licenciada bajo licencias generales, si la interpretación o ejecución de la obra está primordialmente orientada por o dirigida a la obtención de una ventaja comercial o una compensación monetaria privada.
ii.	Regalías por Fonogramas. El Licenciante se reserva el derecho exclusivo de recolectar, individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, SAYCO), una agencia de derechos musicales o algún agente designado, las regalías por cualquier fonograma que Usted cree a partir de la obra (“versión cover”) y distribuya, en los términos del régimen de derechos de autor, si la creación o distribución de esa versión cover está primordialmente destinada o dirigida a obtener una ventaja comercial o una compensación monetaria privada.
e.	Gestión de Derechos de Autor sobre Interpretaciones y Ejecuciones Digitales (WebCasting). Para evitar toda confusión, el Licenciante aclara que, cuando la obra sea un fonograma, el Licenciante se reserva el derecho exclusivo de autorizar la ejecución pública digital de la obra (por ejemplo, webcast) y de recolectar, individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, Acinpro), las regalías por la ejecución pública digital de la obra (por ejemplo, webcast), sujeta a las disposiciones aplicables del régimen de Derecho de Autor, si esta ejecución pública digital está primordialmente dirigida a obtener una ventaja comercial o una compensación monetaria privada.
5. Representaciones, Garantías y Limitaciones de Responsabilidad.
A MENOS QUE LAS PARTES LO ACORDARAN DE OTRA FORMA POR ESCRITO, EL LICENCIANTE OFRECE LA OBRA (EN EL ESTADO EN EL QUE SE ENCUENTRA) “TAL CUAL”, SIN BRINDAR GARANTÍAS DE CLASE ALGUNA RESPECTO DE LA OBRA, YA SEA EXPRESA, IMPLÍCITA, LEGAL O CUALQUIERA OTRA, INCLUYENDO, SIN LIMITARSE A ELLAS, GARANTÍAS DE TITULARIDAD, COMERCIABILIDAD, ADAPTABILIDAD O ADECUACIÓN A PROPÓSITO DETERMINADO, AUSENCIA DE INFRACCIÓN, DE AUSENCIA DE DEFECTOS LATENTES O DE OTRO TIPO, O LA PRESENCIA O AUSENCIA DE ERRORES, SEAN O NO DESCUBRIBLES (PUEDAN O NO SER ESTOS DESCUBIERTOS). ALGUNAS JURISDICCIONES NO PERMITEN LA EXCLUSIÓN DE GARANTÍAS IMPLÍCITAS, EN CUYO CASO ESTA EXCLUSIÓN PUEDE NO APLICARSE A USTED.
6. Limitación de responsabilidad.
A MENOS QUE LO EXIJA EXPRESAMENTE LA LEY APLICABLE, EL LICENCIANTE NO SERÁ RESPONSABLE ANTE USTED POR DAÑO ALGUNO, SEA POR RESPONSABILIDAD EXTRACONTRACTUAL, PRECONTRACTUAL O CONTRACTUAL, OBJETIVA O SUBJETIVA, SE TRATE DE DAÑOS MORALES O PATRIMONIALES, DIRECTOS O INDIRECTOS, PREVISTOS O IMPREVISTOS PRODUCIDOS POR EL USO DE ESTA LICENCIA O DE LA OBRA, AUN CUANDO EL LICENCIANTE HAYA SIDO ADVERTIDO DE LA POSIBILIDAD DE DICHOS DAÑOS. ALGUNAS LEYES NO PERMITEN LA EXCLUSIÓN DE CIERTA RESPONSABILIDAD, EN CUYO CASO ESTA EXCLUSIÓN PUEDE NO APLICARSE A USTED.
7. Término.
a.	Esta Licencia y los derechos otorgados en virtud de ella terminarán automáticamente si Usted infringe alguna condición establecida en ella. Sin embargo, los individuos o entidades que han recibido Obras Derivadas o Colectivas de Usted de conformidad con esta Licencia, no verán terminadas sus licencias, siempre que estos individuos o entidades sigan cumpliendo íntegramente las condiciones de estas licencias. Las Secciones 1, 2, 5, 6, 7, y 8 subsistirán a cualquier terminación de esta Licencia.
b.	Sujeta a las condiciones y términos anteriores, la licencia otorgada aquí es perpetua (durante el período de vigencia de los derechos de autor de la obra). No obstante lo anterior, el Licenciante se reserva el derecho a publicar y/o estrenar la Obra bajo condiciones de licencia diferentes o a dejar de distribuirla en los términos de esta Licencia en cualquier momento; en el entendido, sin embargo, que esa elección no servirá para revocar esta licencia o que deba ser otorgada , bajo los términos de esta licencia), y esta licencia continuará en pleno vigor y efecto a menos que sea terminada como se expresa atrás. La Licencia revocada continuará siendo plenamente vigente y efectiva si no se le da término en las condiciones indicadas anteriormente.
8. Varios.
a.	Cada vez que Usted distribuya o ponga a disposición pública la Obra o una Obra Colectiva, el Licenciante ofrecerá al destinatario una licencia en los mismos términos y condiciones que la licencia otorgada a Usted bajo esta Licencia.
b.	Si alguna disposición de esta Licencia resulta invalidada o no exigible, según la legislación vigente, esto no afectará ni la validez ni la aplicabilidad del resto de condiciones de esta Licencia y, sin acción adicional por parte de los sujetos de este acuerdo, aquélla se entenderá reformada lo mínimo necesario para hacer que dicha disposición sea válida y exigible.
c.	Ningún término o disposición de esta Licencia se estimará renunciada y ninguna violación de ella será consentida a menos que esa renuncia o consentimiento sea otorgado por escrito y firmado por la parte que renuncie o consienta.
d.	Esta Licencia refleja el acuerdo pleno entre las partes respecto a la Obra aquí licenciada. No hay arreglos, acuerdos o declaraciones respecto a la Obra que no estén especificados en este documento. El Licenciante no se verá limitado por ninguna disposición adicional que pueda surgir en alguna comunicación emanada de Usted. Esta Licencia no puede ser modificada sin el consentimiento mutuo por escrito del Licenciante y Usted.

 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