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Published in 2017 at "Biochemical Pharmacology"
DOI: 10.1016/j.bcp.2017.08.026
Abstract: ABSTRACT Sildenafil and tadalafil are widely‐used phosphodiesterase 5 (PDE5) inhibitors for which no clear dose‐response relationship could be established. Using isolated and/or recombinant PDE5, it has been demonstrated that cGMP can increase the affinity of…
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Keywords:
guanosine monophosphate;
sildenafil tadalafil;
tadalafil;
pde5 ... See more keywords
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Published in 2020 at "Bioorganic chemistry"
DOI: 10.1016/j.bioorg.2020.104322
Abstract: Celecoxib, is a selective cyclooxygenase-2 (COX2) inhibitor with a 1,5-diaryl pyrazole scaffold. Celecoxib has a better safety profile compared to other COX2 inhibitors having side effects of systemic hypertension and thromboembolic complications. This may be…
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Keywords:
pyrazolines novel;
pde5 inhibitors;
pde5;
discovery trisubstituted ... See more keywords
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Published in 2017 at "Canadian journal of physiology and pharmacology"
DOI: 10.1139/cjpp-2016-0551
Abstract: The chemotherapeutic use of doxorubicin (Dox) is hindered due to the development of irreversible cardiotoxicity. Specifically, childhood cancer survivors are at greater risk of Dox-induced cardiovascular complications. Because of the potent cardioprotective effect of phosphodiesterase…
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Keywords:
juvenile mice;
pde5;
treatment;
dox treatment ... See more keywords
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Published in 2023 at "Physiology"
DOI: 10.1152/physiol.2023.38.s1.5730553
Abstract: Protein-protein interaction studies have contributed enormously to understand the fundamentals of human impairments including cardiovascular diseases. We previously identified Phosphodiesterase 5 (PDE5) as an interacting partner of RhoBTB1. The latter can function as an adapter…
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Keywords:
pde5;
rhobtb1;
rhobtb1 cul;
cul pathway ... See more keywords
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Published in 2022 at "Current medicinal chemistry"
DOI: 10.2174/0929867329666220216111952
Abstract: BACKGROUND Catalytic hydrolysis of cyclic guanosine monophosphate (cGMP) by phosphodiesterase 6 (PDE6) is a critical step in phototransduction signalling in photoreceptors. Mutations in the genes encoding any of the three PDE6 subunits are associated with…
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Keywords:
expression;
rd1 mice;
photoreceptors rd1;
pde5 ... See more keywords
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Published in 2021 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2021.627229
Abstract: The use of already-approved drugs to treat new or alternative diseases has proved to be beneficial in medicine, because it reduces both drug development costs and timelines. Most drugs can be used to treat different…
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Keywords:
pde5 inhibitor;
pde5 inhibitors;
pde5;
case ... See more keywords
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Published in 2019 at "Cancers"
DOI: 10.3390/cancers11111740
Abstract: The overexpression of phosphodiesterase (PDE) 5 is frequently found in various human cancers, such as those of the breast. However, PDE5’s role in the tumor microenvironment is still unknown. As PDE5 represents a high-value therapeutic…
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Keywords:
pde5;
associated fibroblasts;
breast cancer;
stroma ... See more keywords
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Published in 2022 at "Molecules"
DOI: 10.3390/molecules27123799
Abstract: Plants and their derived molecules have been traditionally used to manage numerous pathological complications, including male erectile dysfunction (ED). Mimosa pudica Linn. commonly referred to as the touch-me-not plant, and its extract are important sources…
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Keywords:
pde5;
bioactive molecules;
simulation;
kcal mol ... See more keywords
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Published in 2023 at "Molecules"
DOI: 10.3390/molecules28093795
Abstract: Glioblastoma (GBM) is the most aggressive brain tumor, with high mortality. Timosaponin AIII (TIA), a steroidal saponin isolated from the medicinal plant Anemarrhena asphodeloides Bge., has been shown to possess anticancer properties in various cancer…
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Keywords:
pde5;
growth;
cgmp;
cell growth ... See more keywords