Results 251 to 260 of about 2,467,830 (354)

Directed C-H activation of 13α-estrone: a pathway to promising AKR1C inhibitors <i>via</i> docking and biological studies. [PDF]

RSC Adv
Mernyák E, Gjorgoška M, Sinreih M, Kotnik A, Zanoškar Z, Godec A, Jukič M, Bren U, Ignácz R, Szőri K, Kele Z, Hunyadi A, Rižner TL.   +12 more
europepmc   +1 more source

Formation of bicyclic pyrroles from the catalytic coupling reaction of 2,5-disubstituted pyrroles with terminal alkynes, involving the activation of multiple C–H bonds

, 2008
Chae S. Yi, Jie Zhang
openalex   +2 more sources

Polarization‐resolved femtosecond Vis/IR spectroscopy tailored for resolving weak signals in biological samples using minimal sample volume

FEBS Open Bio, EarlyView.
Unique biological samples, such as site‐specific mutant proteins, are available only in limited quantities. Here, we present a polarization‐resolved transient infrared spectroscopy setup with referencing to improve signal‐to‐noise tailored towards tracing small signals. We provide an overview of characterizing the excitation conditions for polarization‐
Clark Zahn, Karsten Heyne
wiley   +1 more source

<i>De novo</i> construction of C-O axial chirality <i>via</i> cobalt-catalyzed atroposelective C-H activation/annulation. [PDF]

Chem Sci
Zhang Y, Xie Y, Guo B, Dou Y, Yang D, Niu JL.   +5 more
europepmc   +1 more source

Ligand Directed Pd-Catalyzed C-H Activation: Mechanistic Insights and Synthetic Applications.

, 2012
Kara J. Stowers
openalex   +2 more sources

C2α‐carbanion‐protonating glutamate discloses tradeoffs between substrate accommodation and reaction rate in actinobacterial 2‐hydroxyacyl‐CoA lyase

FEBS Open Bio, EarlyView.
Enzymes of the 2‐hydroxyacyl‐CoA lyase group catalyze the condensation of formyl‐CoA with aldehydes or ketones. Thus, by structural adaptation of active sites, practically any pharmaceutically and industrially important 2‐hydroxyacid could be biotechnologically synthesized. Combining crystal structure analysis, active site mutations and kinetic assays,
Michael Zahn, Barbara Seroka, Ryszard Lazny, Zenon Lotowski, Thore Rohwerder   +4 more
wiley   +1 more source

Selective Functionalization of 1-substituted-3-arylquinoxalin-2(1<i>H</i>)-ones <i>via</i> C-H activation. [PDF]

RSC Adv
Kumar P, Priya, Dutta S, Mishra D, Kumar N.   +4 more
europepmc   +1 more source

PARP inhibitors induce a senescence phenotype in non‐small cell lung carcinoma cell lines

FEBS Open Bio, EarlyView.
Talazoparib is the most potent inducer of senescence among different PARP1 inhibitors in human NSCLC cells. In the absence of PARP, no senescence phenotype was observed, demonstrating that PARP1 is necessary for the induction of senescence by this inhibitor.
Camille Huart, Manon Van den Abbeel, Christoph Schifflers, Karim Bouhjar, Andrea Scarmelotto, Alexis Khelfi, Anne‐Catherine Wera, Carine Michiels   +7 more
wiley   +1 more source

Versatile Butenolide Syntheses via a Structure-Oriented C-H Activation Reaction. [PDF]

J Am Chem Soc
Lin YK, Kim D, Ouyang Y, Yu JQ.
europepmc   +1 more source

Promiscuous stimulation of HSP70 ATPase activity by parasite‐derived J‐domains

FEBS Open Bio, EarlyView.
The malaria parasite Plasmodium falciparum exports three highly homologous yet functionally divergent J‐domain proteins into human erythrocytes. Here, we show that J‐domains isolated from all three proteins effectively stimulate the ATPase activity of both endogenous host and exported parasite HSP70 chaperones.
Julian Barth, Moritz Koch, Le‐Han Rössner, Johanna Eichhorn, Denys Pogoryelov, Matthias P. Mayer, Jude M. Przyborski   +6 more
wiley   +1 more source