Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dominik, Madea"'
Autor:
Dominik Madea, Taufiqueahmed Mujawar, Aleš Dvořák, Kateřina Pospíšilová, Lucie Muchová, Petra Čubáková, Miroslav Kloz, Jakub Švenda, Libor Vítek, Petr Klán
Publikováno v:
The Journal of Organic Chemistry. 87:3089-3103
Autor:
Petr Slavíček, Jakub Švenda, Jiří Janoš, Sadegh Mahvidi, Petr Klán, Jiří Suchan, Dominik Madea, Taufiqueahmed Pirsaheb Mujawar
Publikováno v:
The Journal of Physical Chemistry A. 124:10457-10471
The photochemistry of bilirubin has been extensively studied due to its importance in the phototherapy of hyperbilirubinemia. In the present work, we investigated the ultrafast photodynamics of a bilirubin dipyrrinone subunit, vinylneoxanthobilirubic
Autor:
Dominik, Madea, Taufiqueahmed, Mujawar, Aleš, Dvořák, Kateřina, Pospíšilová, Lucie, Muchová, Petra, Čubáková, Miroslav, Kloz, Jakub, Švenda, Libor, Vítek, Petr, Klán
Publikováno v:
The Journal of organic chemistry. 87(5)
Bilirubin (BR) is an essential metabolite formed by the catabolism of heme. Phototherapy with blue-green light can be applied to reduce high concentrations of BR in blood and is used especially in the neonatal period. In this work, we studied the pho
Publikováno v:
The Journal of Organic Chemistry. 85:3473-3489
Carbon monoxide (CO) is a cell-signaling molecule (gasotransmitter) produced endogenously by oxidative catabolism of heme, and the understanding of its spatial and temporal sensing at the cellular level is still an open challenge. Synthesis, optical
Autor:
Lucie Muchová, Jiří Janoš, Petr Slavíček, Libor Vítek, Dominik Madea, Jakub Švenda, David Chalupa, Sadegh Mahvidi, Petr Klán, Aleš Dvořák, Taufiqueahmed Pirsaheb Mujawar
Publikováno v:
The Journal of organic chemistry. 85(20)
Phototherapy is a standard treatment for severe neonatal jaundice to remove toxic bilirubin from the blood. Here, the wavelength-dependent photochemistry of vinylneoxanthobilirubic acid methyl ester, a simplified model of a bilirubin dipyrrinone subu
Publikováno v:
Chemical Communications. 52:12901-12904
A bioorthogonal 'catch and photorelease' strategy, which combines alkyne-azide cycloaddition between p-hydroxyphenacyl azide and alkyne derivatives to form a 1,2,3-triazole adduct and subsequent photochemical release of the triazole moiety via a phot