Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Maodie Wang"'
Publikováno v:
ACS Omega, Vol 3, Iss 5, Pp 5502-5510 (2018)
Externí odkaz:
https://doaj.org/article/80b9155807024456b2cf8b9c1d4780dc
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 25:696-702
The synthesis of a chlorin e6-nevirapine conjugate is reported, in which the nevirapine moiety is attached to the 131-position of chlorin e6 via a diethylene glycol linker. This conjugate was found to be nontoxic in the dark (IC[Formula: see text] >
Autor:
Giampaolo Barone, Evamarie Hey-Hawkins, Guanyu Zhang, Maodie Wang, Maria Rangel, José Domingues de Almeida, Ana F R Cerqueira, Augusto C. Tomé, M. Graça H. Vicente, Ana M. G. Silva, Carla Queirós
Publikováno v:
Organic & Biomolecular Chemistry. 19:6501-6512
Indomethacin is a potent non-steroidal anti-inflammatory drug (NSAID) with a strong selective inhibitor activity towards cyclooxygenase-2 (COX-2), an enzyme that is highly overexpressed in various tumour cells, being involved in tumourigenesis. Conco
Autor:
Guanyu Zhang, Maodie Wang, Petia Bobadova‐Parvanova, Frank R. Fronczek, Kevin M. Smith, M. Graça H. Vicente
Publikováno v:
Chemistry – A European Journal. 28
The synthesis and reactivity of 3,8-dibromo-dodecafluoro-benzo-fused BOPHY 2 are reported, via S
Autor:
Petia Bobadova-Parvanova, Maodie Wang, Caroline Ndung’U, Frank R. Fronczek, Guanyu Zhang, M. Graça H. Vicente, Kevin M. Smith
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 24:869-877
Three BODIPYs bearing 1,3,5,7-tetramethyl substituents and a meso-8-aryl group were synthesized and investigated, both experimentally and computationally. The presence of the 1,7-methyl groups and of ortho-substituents on the meso-8-aryl ring prevent
Autor:
Kevin M. Smith, M. Graça H. Vicente, Maodie Wang, Frank R. Fronczek, Petia Bobadova-Parvanova, Nichole E. M. Kaufman, Guanyu Zhang
Publikováno v:
European Journal of Organic Chemistry. 2020:971-977
Publikováno v:
The Journal of Organic Chemistry
A series of α-amino acid-BODIPY derivatives were synthesized using commercially available N-Boc-l-amino acids, via boron functionalization under mild conditions. The mono-linear, mono-spiro, and di-amino acid-BODIPY derivatives were obtained using a
Autor:
Kevin M. Smith, Lilian Odom, Petia Bobadova-Parvanova, Frank R. Fronczek, Maodie Wang, David Barbosa, M. Graça H. Vicente, Guanyu Zhang, Ashley N. Merriweather
Publikováno v:
Inorganic Chemistry. 58:11614-11621
An efficient synthesis of boron-functionalized cyclic BODIPY-Gly conjugates, using commercially available N-protected glycine amino acids and a BF2-BODIPY moiety as starting materials, is reported. The existence of two conformers (up and down) is rev
Publikováno v:
Inorganic Chemistry. 57:14493-14496
A novel and straightforward strategy for boron functionalization in boron dipyrromethenes (BODIPYs) is developed. In particular, this synthetic strategy provides new possibilities for the synthesis of sp2 N-substituted (B-NCS and -NCO), benzotriazole
Autor:
Luciana Amaral de Mascena Costa, Manoel Adrião Gomes Filho, Rodrigo da Silva Viana, Maodie Wang, Janaína V. dos Anjos, Andressa Nathally Rocha Leal, Ashlyn C. Harmon, Rafael Cueto, Maria da Graça H. Vicente, Severino Alves Júnior, Guanyu Zhang, J. Michael Mathis, Tyrslai M. Williams, Liquian Luan, Eduardo H.L. Falcão
Publikováno v:
Journal of Nanoparticle Research. 21
Colon cancer is one of the world’s most deadly diseases. Because of its internal location, it is necessary to obtain faster and more efficient diagnostic tools for this organ site. In this context, we studied the development of new luminescent nano