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Image Search Results
Journal: Archives of biochemistry and biophysics
Article Title: Identifying novel aryl hydrocarbon receptor (AhR) modulators from clinically approved drugs: In silico screening and In vitro validation.
doi: 10.1016/j.abb.2024.109958
Figure Lengend Snippet: Fig. 5. Evolutions of structural properties of complex via RMSD over time (200ns) in of AhR ligands. A) stability of bound complexes with flibanserin, butoconazol, luliconazole, naftifine, and triclabendazole in presence of PAS-B alone. B) stability of bound complexes with rosiglitazone, empagliflozin, benperidol, nebivolol, and zucapsaicin.
Article Snippet:
Techniques:
Journal: Archives of biochemistry and biophysics
Article Title: Identifying novel aryl hydrocarbon receptor (AhR) modulators from clinically approved drugs: In silico screening and In vitro validation.
doi: 10.1016/j.abb.2024.109958
Figure Lengend Snippet: Fig. 4. Evolutions of structural properties of the ligand heavy atoms via RMSD over time (200ns). A) stability of flibanserin, butoconazol, luliconazole, naftifine, and triclabendazole in presence of PAS-B alone. B) stability of rosiglitazone, empagliflozin, benperidol, nebivolol, and zucapsaicin.
Article Snippet:
Techniques:
Journal: Archives of biochemistry and biophysics
Article Title: Identifying novel aryl hydrocarbon receptor (AhR) modulators from clinically approved drugs: In silico screening and In vitro validation.
doi: 10.1016/j.abb.2024.109958
Figure Lengend Snippet: Fig. 7. mode of binding from predominate cluster for each drug A) Flibanserin, B) Zucapsaicin, C) Rosiglitazone, D) Triclabendazole, E) Butoconazole, F) Benperidol, G) Naftifine, H) Nebivolol, I) Empagliflozin, and J) Luliconazole.
Article Snippet:
Techniques: Binding Assay
Journal: Archives of biochemistry and biophysics
Article Title: Identifying novel aryl hydrocarbon receptor (AhR) modulators from clinically approved drugs: In silico screening and In vitro validation.
doi: 10.1016/j.abb.2024.109958
Figure Lengend Snippet: Fig. 6. Beta factor per residue backbone atoms over 200 ns MD trajectory in present of unbound protein (PAS-B) as reference and bound protein to ten selected drugs. A) Flibanserin, butoconazol, luliconazole, naftifine, and triclabendazole in presence of PAS-B alone. B) Rosiglitazone, empagliflozin, benperidol, nebivolol, and zucapsaicin.
Article Snippet:
Techniques: Residue
Journal: Therapeutic Advances in Chronic Disease
Article Title: Flibanserin for hypoactive sexual desire disorder: place in therapy
doi: 10.1177/2040622316679933
Figure Lengend Snippet: Structure of Flibanserin. Sprout Pharmaceuticals Inc., 2015.
Article Snippet: [ PubMed ]
Techniques:
Journal: Therapeutic Advances in Chronic Disease
Article Title: Flibanserin for hypoactive sexual desire disorder: place in therapy
doi: 10.1177/2040622316679933
Figure Lengend Snippet: Mean + SD Plasma Flibanserin Concentration-Time Profiles in Healthy Female Subjects Following a Single Oral Dose of 100mg of Flibanserin (Linear Scale). Sprout Pharmaceuticals Inc., 2015.
Article Snippet: [ PubMed ]
Techniques: Clinical Proteomics, Concentration Assay
Journal: Pharmaceuticals
Article Title: Cardioprotective Effect of Flibanserin against Isoproterenol-Induced Myocardial Infarction in Female Rats: Role of Cardiac 5-HT2A Receptor Gene/5-HT/Ca 2+ Pathway
doi: 10.3390/ph16040502
Figure Lengend Snippet: The ECG examination in different treated groups. ( a ): The electrocardiographic effect of FLP in different doses on ISO-induced MI in rats. ( b ): ECG in experimental rats pretreated with FLP (15, 30, and 45 mg/kg) in an ISO-induced MI model on HR, QT interval, R amplitude, and ST segment amplitude. ( A ) Normal group, ( B ) Iso group, ( C ) FLB 15 mg + Iso group, ( D ) FLB 30 mg + Iso group and FLB 45 mg + Iso group. Bars with different letters are significantly different according to DMRT at p < 0.001 level ( n = 5). Data are expressed as Mean ± SD. ECG = electrocardiogram, FLP = flibanserin, ISO = isoproterenol, MI = myocardial infarction, HR = heart rate, DMRT = Duncan’s multiple range test.
Article Snippet:
Techniques:
Journal: Pharmaceuticals
Article Title: Cardioprotective Effect of Flibanserin against Isoproterenol-Induced Myocardial Infarction in Female Rats: Role of Cardiac 5-HT2A Receptor Gene/5-HT/Ca 2+ Pathway
doi: 10.3390/ph16040502
Figure Lengend Snippet: Histopathological examination in the different treated groups. ( A ): Photomicrograph for specimens from the heart stained with H&E 10× & 40× in different treated groups. In the normal group: [H&E 10×] shows Compact, uniformly arranged myocardial fibers (Black arrows), [H&E 40×] myocytes show preserved uniform nuclei (Black arrows) and cytoplasmic cross striation (Red arrows). In ISO group: [H&E 10×] shows a wide separation of myocardial fibers due to interstitial edema (Black arrows), areas of myocardial fibers loss of eosinophilic staining and becoming pallor in appearance (Arrowheads), the influx of inflammatory cells into myocardial fibers (Red arrows), [H&E 40×] shows pathological changes of MI, interstitial edema between myocardial fibers (Black arrows), loss of cytoplasmic striation of myocytes with shrinkage of nuclei and prominence of the cell membrane (Arrowheads), some myocytes show an absence of nuclei (Yellow arrows), the influx of macrophages, indicating an inflammatory response to remove dead fibers (Red arrows). In FLP (15 mg/kg) + ISO group: [H&E 10×] shows no significant difference when compared to the ISO group as there is still a wide separation of myocardial fibers due to interstitial edema (Black arrows), the influx of inflammatory cells into myocardial fibers (Red arrows), [H&E 40×] shows persistent pathological changes of MI, interstitial edema between myocardial fibers (Black arrows), loss of cytoplasmic striation of myocytes with shrinkage of nuclei and prominence of the cell membrane (Arrowheads), some myocytes show an absence of nuclei (Yellow arrows), the influx of macrophages indicating an inflammatory response to remove dead fibers (Red arrows). In FLP (30 mg/kg) + ISO group: [H&E 10×] still shows interstitial edema (Black arrows); however, a slight reduction in inflammatory cell influx is noticed (Red arrow), [H&E 40×] shows persistent pathological changes of MI, yet to a milder degree: interstitial edema between myocardial fibers (Black arrows), loss of cytoplasmic striation of few myocytes with shrinkage of nuclei and prominence of the cell membrane (Arrowheads), absence of nuclei in few myocytes (Yellow arrows), reduction in macrophages influx (Red arrows). In FLP (45 mg/kg) + ISO group: [H&E 10×] shows compact uniformly arranged myocardial fibers and absence of interstitial edema (Black arrows); few areas of chronic inflammatory cells are seen (Red arrow), [H&E 40×] myocytes show uniform nuclei and eosinophilic cytoplasm (Black arrows), few macrophages are seen (Red arrows). ( B ): histopathologic score in experimental rats pretreated with FLP (15, 30, and 45 mg/kg) in an ISO-induced MI model. Data were analyzed using Kruskal-Wallis followed by Dunn’s test for multiple comparisons against the normal group at p < 0.05., ** p < 0.01, *** p < 0.001, n = 6. H&E = hematoxylin and eosin, FLP = flibanserin, ISO = isoproterenol, MI = myocardial infarction.
Article Snippet:
Techniques: Staining, Membrane
Journal: Pharmaceuticals
Article Title: Cardioprotective Effect of Flibanserin against Isoproterenol-Induced Myocardial Infarction in Female Rats: Role of Cardiac 5-HT2A Receptor Gene/5-HT/Ca 2+ Pathway
doi: 10.3390/ph16040502
Figure Lengend Snippet: Serum cardiac enzymes levels in experimental rats pretreated with FLP (15, 30, and 45 mg/kg) in an ISO-induced MI model ( A ): The cardiac serum level of Tnl ( B ): The cardiac serum level of CK-MB, ( C ): The cardiac serum level of LDH. ( D ): The cardiac serum level of CK. Bars with different letters are significantly different according to DMRT at p < 0.001 level ( n = 5). Data are expressed as Mean ± SD. FLP = flibanserin, ISO = isoproterenol, MI = myocardial infarction, Tnl = troponin I, CK-MB = creatinine kinase-MB, LDH = lactate dehydrogenase, CK = creatine kinase, DMRT = Duncan’s multiple range test.
Article Snippet:
Techniques:
Journal: Pharmaceuticals
Article Title: Cardioprotective Effect of Flibanserin against Isoproterenol-Induced Myocardial Infarction in Female Rats: Role of Cardiac 5-HT2A Receptor Gene/5-HT/Ca 2+ Pathway
doi: 10.3390/ph16040502
Figure Lengend Snippet: Effect of FLP in different doses on heart tissue level of GSH and MDA. ( A ): Heart level of GSH in experimental rats pretreated with FLP (15, 30, and 45 mg/kg) in an ISO-induced MI model. ( B ) Heart level of MDA in experimental rats pretreated with FLP (15, 30, and 45 mg/kg) in an ISO-induced MI model. Bars with different letters are significantly different according to DMRT at p < 0.001 level ( n = 5). Data are expressed as Mean ± SD. FLP = flibanserin, GSH = reduced glutathione, MDA = malondialdehyde, ISO = isoproterenol, DMRT = Duncan’s multiple range test.
Article Snippet:
Techniques:
Journal: Pharmaceuticals
Article Title: Cardioprotective Effect of Flibanserin against Isoproterenol-Induced Myocardial Infarction in Female Rats: Role of Cardiac 5-HT2A Receptor Gene/5-HT/Ca 2+ Pathway
doi: 10.3390/ph16040502
Figure Lengend Snippet: Proposed FLP action on DA, NE, and 5-HT centers of the brain. The figure represents the dopaminergic system ( A ) before and ( B ) after the administration of flibanserin. While noradrenergic system ( C ) before and ( D ) after administration of flibanserin. Finally, serotonergic system ( E ) before and ( F ) after administration of flibanserin. Glu = Glutamate, GABA = Gamma-aminobutyric acid, NE = Norepinephrine, DA = Dopamine, 5-HT = Serotonin, FLP = Flibanserin.
Article Snippet:
Techniques:
Journal: Therapeutic Advances in Chronic Disease
Article Title: Flibanserin for hypoactive sexual desire disorder: place in therapy
doi: 10.1177/2040622316679933
Figure Lengend Snippet: Structure of Flibanserin. Sprout Pharmaceuticals Inc., 2015.
Article Snippet: The purpose of this program is to inform providers and patients of the hypotension and syncope that occur when
Techniques:
Journal: Therapeutic Advances in Chronic Disease
Article Title: Flibanserin for hypoactive sexual desire disorder: place in therapy
doi: 10.1177/2040622316679933
Figure Lengend Snippet: Mean + SD Plasma Flibanserin Concentration-Time Profiles in Healthy Female Subjects Following a Single Oral Dose of 100mg of Flibanserin (Linear Scale). Sprout Pharmaceuticals Inc., 2015.
Article Snippet: The purpose of this program is to inform providers and patients of the hypotension and syncope that occur when
Techniques: Clinical Proteomics, Concentration Assay