Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Enrique Alvarado-Martínez"'
Autor:
Ainhoa Oliden-Sánchez, Enrique Alvarado-Martínez, Diana E. Ramírez-Ornelas, Miguel A. Vázquez, Edurne Avellanal-Zaballa, Jorge Bañuelos, Eduardo Peña-Cabrera
Publikováno v:
Molecules, Vol 28, Iss 12, p 4750 (2023)
Herein, we report the synthetic access to a set of π-extended BODIPYs featuring a penta-arylated (phenyl and/or thiophene) dipyrrin framework. We take advantage of the full chemoselective control of 8-methylthio-2,3,5,6-tetrabromoBODIPY when we cond
Externí odkaz:
https://doaj.org/article/6abae8db830f4f68bf1d7312f238c41d
Autor:
Samira Husen Alamudi, Rudrakanta Satapathy, Jihyo Kim, Dongdong Su, Haiyan Ren, Rajkumar Das, Lingna Hu, Enrique Alvarado-Martínez, Jung Yeol Lee, Christian Hoppmann, Eduardo Peña-Cabrera, Hyung-Ho Ha, Hee-Sung Park, Lei Wang, Young-Tae Chang
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
The success of a fluorescent dye as a molecular probe to monitor the intracellular activity of biomolecules depends on its physicochemical characteristics. Here, the authors use a predictive model to identify key features that allow them to design ce
Externí odkaz:
https://doaj.org/article/1ffa76b518c2484e9d9435cbbf2eabe7
Autor:
Peña-Cabrera, Ainhoa Oliden-Sánchez, Enrique Alvarado-Martínez, Diana E. Ramírez-Ornelas, Miguel A. Vázquez, Edurne Avellanal-Zaballa, Jorge Bañuelos, Eduardo
Publikováno v:
Molecules; Volume 28; Issue 12; Pages: 4750
Herein, we report the synthetic access to a set of π-extended BODIPYs featuring a penta-arylated (phenyl and/or thiophene) dipyrrin framework. We take advantage of the full chemoselective control of 8-methylthio-2,3,5,6-tetrabromoBODIPY when we cond
Autor:
Carlos A. Osorio-Martı́nez, Juan O. Flores-Rizo, Iñigo López Arbeloa, Brenda Daniela Gutierrez-Ramos, Rongrong Hu, Erik Lager, Ben Zhong Tang, Lourdes Betancourt-Mendiola, Arlette Urías-Benavides, Ismael J. Arroyo, Enrique Alvarado-Martínez, Ismael Valois-Escamilla, Teresa Arbeloa, José L. Belmonte-Vázquez, Jorge Bañuelos, Mayra R. Martinez-Gonzalez, Eduardo Peña-Cabrera, César F. A. Gómez-Durán
Publikováno v:
The Journal of Organic Chemistry. 80:5771-5782
Several new examples of meso-(het)arylBODIPY were prepared via the Liebeskind-Srogl (L-S) cross-coupling reaction of the Biellmann BODIPYs (1a,b) and aryl- and heteroarylboronic acids in good to excellent yield. It was shown that this reaction could
Autor:
Teresa Arbeloa, Angel Costela, Inmaculada García, Mayca del Rio, Arlette Urías-Benavides, Jorge Bañuelos, J. Cristobal Lopez, Mayra R. Martinez-Gonzalez, Eduardo Peña-Cabrera, Ana M. Gómez, Iñigo López Arbeloa, Enrique Alvarado-Martínez
Publikováno v:
European Journal of Organic Chemistry. 2014:5659-5663
Two complementary one-pot, three component synthetic strategies based on copper(I)-catalyzed azide–alkyne cycloadditions (CuAAC) have been developed, which allow the efficient assembly of glycosyl-derived alkynes or azides with highly fluorescent b
Autor:
Iñigo López Arbeloa, Enrique Alvarado-Martínez, Teresa Arbeloa, Luis A. Pérez-García, Diana E. Ramírez-Ornelas, Eduardo Peña-Cabrera, Héctor M. Mora-Montes, Jorge Bañuelos
Publikováno v:
ChemInform. 47
Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebeskind–Srogl cross-coupling reaction or the Vilsmeier reaction. These dyes were used as components in the Passerini reaction to give highly substituted BODIPY dyes. A joi
Autor:
Lingna Hu, Enrique Alvarado-Martínez, Young-Tae Chang, Hee-Sung Park, Rudrakanta Satapathy, Christian Hoppmann, Jihyo Kim, Eduardo Peña-Cabrera, Lei Wang, Haiyan Ren, Samira Husen Alamudi, Dongdong Su, Raj Kumar Das, Jung Yeol Lee, Hyung-Ho Ha
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
Alamudi, SH; Satapathy, R; Kim, J; Su, D; Ren, H; Das, R; et al.(2016). Development of background-free tame fluorescent probes for intracellular live cell imaging. NATURE COMMUNICATIONS, 7. doi: 10.1038/ncomms11964. UCSF: Retrieved from: http://www.escholarship.org/uc/item/6k59t0vp
Nature Communications
Nature communications, vol 7, iss 1
Alamudi, SH; Satapathy, R; Kim, J; Su, D; Ren, H; Das, R; et al.(2016). Development of background-free tame fluorescent probes for intracellular live cell imaging. NATURE COMMUNICATIONS, 7. doi: 10.1038/ncomms11964. UCSF: Retrieved from: http://www.escholarship.org/uc/item/6k59t0vp
Nature Communications
Nature communications, vol 7, iss 1
Fluorescence labelling of an intracellular biomolecule in native living cells is a powerful strategy to achieve in-depth understanding of the biomolecule's roles and functions. Besides being nontoxic and specific, desirable labelling probes should be
Autor:
Iñigo López Arbeloa, Eduardo Peña-Cabrera, Teresa Arbeloa, Luis A. Pérez-García, Diana E. Ramírez-Ornelas, Enrique Alvarado-Martínez, Héctor M. Mora-Montes, Jorge Bañuelos
Publikováno v:
The Journal of organic chemistry. 81(7)
Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebeskind–Srogl cross-coupling reaction or the Vilsmeier reaction. These dyes were used as components in the Passerini reaction to give highly substituted BODIPY dyes. A joi
Autor:
Enrique Alvarado Martínez
Publikováno v:
Encuentro, Iss 79, Pp 04-07 (2008)
El autor describe en forma sucinta la vitalidad senera del aporte teorico del Sacerdote Jesuita Xabier Gorostiaga (q.e.p.d.), quien segun el “predecia el futuro, mientras repasaba el pasado”. Enfatiza, retomando el enunciado del educador y pedago
Autor:
Eduardo Peña-Cabrera, Richard W. Horobin, Young-Tae Chang, Enrique Alvarado-Martínez, Shohei Uchinomiya
Publikováno v:
Combinatorial chemistryhigh throughput screening. 19(5)
Control of fluorescent dye localization in live cells is crucial for fluorescence imaging. Here, we describe quantitative structure activity relation (QSAR) models for predicting intracellular localization of fluorescent dyes. For generating the QSAR