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Titlebook: Reactive Oxygen Species; Network Pharmacology Harald H. H. W. Schmidt,Pietro Ghezzi,Antonio Cuad Book 2021 Springer Nature Switzerland AG 2

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31#
發(fā)表于 2025-3-26 21:04:43 | 只看該作者
Soluble Guanylate Cyclase Stimulators and Activators heme-containing and oxidized, heme-free sGC, respectively, which results in an increase in cGMP production. The action of sGC stimulators at the heme-containing enzyme is independent of NO but is enhanced in the presence of NO whereas the sGC activators interact with the heme-free form of sGC. Thes
32#
發(fā)表于 2025-3-27 05:01:49 | 只看該作者
Book 2021emain the same and this book will thus become, and for many years remain, the leadingreference for ROSopathies and their treatment by network pharmacology.??. .Chapter "Soluble Guanylate Cyclase Stimulators and Activators" is available open access under a Creative Commons Attribution 4.0 Internation
33#
發(fā)表于 2025-3-27 07:39:58 | 只看該作者
0171-2004 ence for ROSopathies and their treatment by network pharmacology.??. .Chapter "Soluble Guanylate Cyclase Stimulators and Activators" is available open access under a Creative Commons Attribution 4.0 Internation978-3-030-68512-6978-3-030-68510-2Series ISSN 0171-2004 Series E-ISSN 1865-0325
34#
發(fā)表于 2025-3-27 12:21:01 | 只看該作者
Book 2021exemplified by the failure of the so-called anti-oxidants. This book is a game changer for the field and many clinical areas such as cardiology and neurology. The term ‘oxidative stress’ is abandoned and replaced with a systems medicine and network pharmacology-based mechanistic approach to disease.
35#
發(fā)表于 2025-3-27 16:20:28 | 只看該作者
36#
發(fā)表于 2025-3-27 19:12:27 | 只看該作者
37#
發(fā)表于 2025-3-27 22:10:32 | 只看該作者
38#
發(fā)表于 2025-3-28 04:45:20 | 只看該作者
Development of Telintra as an Inhibitor of Glutathione S-Transferase Pn certain tumors and is over-expressed in cancer drug resistance. It has diverse cellular functions that include, thiolase activities with small electrophilic agents or susceptible cysteine residues on the protein to mediate S-glutathionylation, and chaperone binding with select protein kinases. Pre
39#
發(fā)表于 2025-3-28 06:22:20 | 只看該作者
40#
發(fā)表于 2025-3-28 12:53:48 | 只看該作者
NOX Inhibitors: From Bench to Naxibs to Bedsideions. Pathophysiology arises when ROS are generated either in excess or in cell types or subcellular locations that normally do not produce ROS or when non-physiological types of ROS (e.g., superoxide instead of hydrogen peroxide) are formed. In the latter scenario, antioxidants were considered as t
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