fda approved compound library Search Results


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Prestwick Chemical fda- and ema-approved compounds
Fda And Ema Approved Compounds, supplied by Prestwick Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioAscent Discovery compound library screens fda-approved
Compound Library Screens Fda Approved, supplied by BioAscent Discovery, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Johns Hopkins HealthCare fda-approved drug library johns hopkins clinical compound library (jhccl) version 1.0
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Fda Approved Drug Library Johns Hopkins Clinical Compound Library (Jhccl) Version 1.0, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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AnalytiCon Discovery GmbH compound libraries comprising of fda-approved drugs, synthetic and semi-synthetic natural products as well as bioactives
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Compound Libraries Comprising Of Fda Approved Drugs, Synthetic And Semi Synthetic Natural Products As Well As Bioactives, supplied by AnalytiCon Discovery GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pharmakon Pharmaceuticals Inc fda approved compounds
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Fda Approved Compounds, supplied by Pharmakon Pharmaceuticals Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ApexBio clinically approved compounds from apexbio fda-approved drug library
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Clinically Approved Compounds From Apexbio Fda Approved Drug Library, supplied by ApexBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Johns Hopkins HealthCare johns hopkins chemcore fda-approved compound library
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Johns Hopkins Chemcore Fda Approved Compound Library, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pharmakon Pharmaceuticals Inc library of 1,600 fda-approved compounds
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
Library Of 1,600 Fda Approved Compounds, supplied by Pharmakon Pharmaceuticals Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Enzo Biochem 640 fda approved compounds
Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="250" height="auto" />
640 Fda Approved Compounds, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Topscience Co Ltd fda approved drugs and bioactive compounds
Identification of TDP25 degrader by high-throughput screening. (A) . Flowchart of the drug screening and its results. (B) . H4GT25 cells were pretreated with 1 μg/mL DOX (doxycycline) for 24 h, incubated with 2110 FDA approved drugs and <t>bioactive</t> compounds for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of scatter diagram. Skyblue and pink colors represent the degree of increase and decrease of GFP-TDP25 expression, respectively, following drug treatments. Shown in black scatterplot is MG132, and shown in red are ibudilast, ouabain, and SC75741. (C) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of blue heatmap. (D) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of red heatmap. (E) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, *** p < 0.001, * p < 0.05, two-tailed t test). (F) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, two-tailed t test). (G) . Chemical structure of SC75741.
Fda Approved Drugs And Bioactive Compounds, supplied by Topscience Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biomol GmbH fda-approved unique drugs and bioactive compounds nihcc lopac biomol iccb known bioactives microsource spectrum
Identification of TDP25 degrader by high-throughput screening. (A) . Flowchart of the drug screening and its results. (B) . H4GT25 cells were pretreated with 1 μg/mL DOX (doxycycline) for 24 h, incubated with 2110 FDA approved drugs and <t>bioactive</t> compounds for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of scatter diagram. Skyblue and pink colors represent the degree of increase and decrease of GFP-TDP25 expression, respectively, following drug treatments. Shown in black scatterplot is MG132, and shown in red are ibudilast, ouabain, and SC75741. (C) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of blue heatmap. (D) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of red heatmap. (E) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, *** p < 0.001, * p < 0.05, two-tailed t test). (F) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, two-tailed t test). (G) . Chemical structure of SC75741.
Fda Approved Unique Drugs And Bioactive Compounds Nihcc Lopac Biomol Iccb Known Bioactives Microsource Spectrum, supplied by Biomol GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Enzo Biochem fda-approved compound decks
Identification of TDP25 degrader by high-throughput screening. (A) . Flowchart of the drug screening and its results. (B) . H4GT25 cells were pretreated with 1 μg/mL DOX (doxycycline) for 24 h, incubated with 2110 FDA approved drugs and <t>bioactive</t> compounds for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of scatter diagram. Skyblue and pink colors represent the degree of increase and decrease of GFP-TDP25 expression, respectively, following drug treatments. Shown in black scatterplot is MG132, and shown in red are ibudilast, ouabain, and SC75741. (C) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of blue heatmap. (D) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of red heatmap. (E) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, *** p < 0.001, * p < 0.05, two-tailed t test). (F) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, two-tailed t test). (G) . Chemical structure of SC75741.
Fda Approved Compound Decks, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Summary of the drug/compound libraries used in the antifungal drug repurposing (see also <xref ref-type= Table S1, Supplementary Materials )." width="100%" height="100%">

Journal: Antibiotics

Article Title: Antifungal Drug Repurposing

doi: 10.3390/antibiotics9110812

Figure Lengend Snippet: Summary of the drug/compound libraries used in the antifungal drug repurposing (see also Table S1, Supplementary Materials ).

Article Snippet: 1547 or 1581 FDA-approved drug library , Johns Hopkins, USA Johns Hopkins Clinical Compound Library (JHCCL) version 1.0 , C. albicans, C. auris, C. krusei, C. parapsilosis, C. tropicalis , [ , ] .

Techniques: Drug discovery

Identification of TDP25 degrader by high-throughput screening. (A) . Flowchart of the drug screening and its results. (B) . H4GT25 cells were pretreated with 1 μg/mL DOX (doxycycline) for 24 h, incubated with 2110 FDA approved drugs and bioactive compounds for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of scatter diagram. Skyblue and pink colors represent the degree of increase and decrease of GFP-TDP25 expression, respectively, following drug treatments. Shown in black scatterplot is MG132, and shown in red are ibudilast, ouabain, and SC75741. (C) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of blue heatmap. (D) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of red heatmap. (E) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, *** p < 0.001, * p < 0.05, two-tailed t test). (F) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, two-tailed t test). (G) . Chemical structure of SC75741.

Journal: Frontiers in Pharmacology

Article Title: SC75741, A Novel c-Abl Inhibitor, Promotes the Clearance of TDP25 Aggregates via ATG5-Dependent Autophagy Pathway

doi: 10.3389/fphar.2021.741219

Figure Lengend Snippet: Identification of TDP25 degrader by high-throughput screening. (A) . Flowchart of the drug screening and its results. (B) . H4GT25 cells were pretreated with 1 μg/mL DOX (doxycycline) for 24 h, incubated with 2110 FDA approved drugs and bioactive compounds for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of scatter diagram. Skyblue and pink colors represent the degree of increase and decrease of GFP-TDP25 expression, respectively, following drug treatments. Shown in black scatterplot is MG132, and shown in red are ibudilast, ouabain, and SC75741. (C) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of blue heatmap. (D) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, incubated with 178 hits for 24 h, and the GFP-TDP25 fluorescence was analyzed by fluorescence microscopy and compared with cells treated with DMSO. The results were presented in the forms of red heatmap. (E) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with arsenite (0.5 mM) for 1 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, *** p < 0.001, * p < 0.05, two-tailed t test). (F) . H4GT25 cells were pretreated with 1 μg/mL DOX for 24 h, treated with MG132 (1 μM) for 12 h, and treated with ibudilast (10 μM), SC75741 (10 μM) or ouabain (10 μM) for another 24 h, fluorescence of GFP-TDP25 was analyzed by fluorescence microscopy and Cell viability was determined using CellTiterGlo ® assay (data represents Mean ± SD.; n = 8, **** p < 0.0001, two-tailed t test). (G) . Chemical structure of SC75741.

Article Snippet: All FDA approved drugs and bioactive compounds were commercially purchased from Topscience, Inc. (Shanghai, China).

Techniques: High Throughput Screening Assay, Drug discovery, Incubation, Fluorescence, Microscopy, Expressing, Two Tailed Test