sulfanilamid Search Results


sia enamine  (Enamine Ltd)
92
Enamine Ltd sia enamine
Sia Enamine, supplied by Enamine Ltd, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulphanilamide  (LGC Standards)
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LGC Standards sulphanilamide
Sulphanilamide, supplied by LGC Standards, 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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filters  (Thermo Fisher)
92
Thermo Fisher filters
Filters, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfamethoxazole  (Valiant Co Ltd)
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Valiant Co Ltd sulfamethoxazole
Sulfamethoxazole, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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trimethoprim sulfamethoxazole  (Chem Impex International)
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Chem Impex International trimethoprim sulfamethoxazole
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sulfanilamide  (Valiant Co Ltd)
93
Valiant Co Ltd sulfanilamide
Sulfanilamide, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfanilamide  (MedChemExpress)
92
MedChemExpress sulfanilamide
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
Sulfanilamide, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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2 methyl 4 isothiazolin 3 one mit  (Aladdin Scientific Corporation)
92
Aladdin Scientific Corporation 2 methyl 4 isothiazolin 3 one mit
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
2 Methyl 4 Isothiazolin 3 One Mit, supplied by Aladdin Scientific Corporation, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfisoxazole  (Valiant Co Ltd)
86
Valiant Co Ltd sulfisoxazole
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
Sulfisoxazole, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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batch n  (European Directorate for the Quality of Medicines and HealthCare)
88
European Directorate for the Quality of Medicines and HealthCare batch n
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
Batch N, supplied by European Directorate for the Quality of Medicines and HealthCare, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfanilamide  (Chem Impex International)
95
Chem Impex International sulfanilamide
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
Sulfanilamide, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfanilamide/n-(1-naphthyl) ethylenediamine dihydrochloride solution #r2233500  (Ricca Chemical Company)
90
Ricca Chemical Company sulfanilamide/n-(1-naphthyl) ethylenediamine dihydrochloride solution #r2233500
Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, <t>sulfanilamide,</t> mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.
Sulfanilamide/N (1 Naphthyl) Ethylenediamine Dihydrochloride Solution #R2233500, supplied by Ricca Chemical Company, 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


Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, sulfanilamide, mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.

Journal: ACS Nano

Article Title: Single-Molecule-Based, Label-Free Monitoring of Molecular Glue Efficacies for Promoting Protein–Protein Interactions Using YaxAB Nanopores

doi: 10.1021/acsnano.4c11436

Figure Lengend Snippet: Specific detection of rapamycin from a mixture of compounds. (a) Schematic illustration of molecular glue detection using a YaxAB-C 9 nanopore. The colored shapes symbolize nonbinding compounds (astemizole, terfenadine, capecitabine, sulfanilamide, mibefradil, pranlukast, dimantine, and monobenzone). (b–d) Representative current traces and statistical analysis of 2D scatter plots (Δ I / I o versus dwell time) and statistical histograms corresponding to the detection of mTOR, FKBP12 (b), and mTOR, FKBP12 with a mixture of nonbinding compounds in the absence (c) or presence (d) of rapamycin. All of the small-molecule compounds were treated at a concentration of 1.6 μM to the cis side of a YaxAB-C 9 nanopore. All of the electrical measurements were performed at an applied potential of +60 mV. Current traces were filtered with a Bessel (8-pole) filter at 1 kHz.

Article Snippet: The small-molecule drugs rapamycin (914.18 g/mol, Selleckchem, Houston), ascomycin (792.01 g/mol, Selleckchem, Houston), temsirolimus (1030.29 g/mol, Selleckchem, Houston), astemizole (458.57 g/mol, MedChemExpress, New Jersey), terfenadine (471.67 g/mol, MedChemExpress), capecitabine (359.35 g/mol, MedChemExpress), sulfanilamide (172.20 g/mol, MedChemExpress), mibefradil (568.55 g/mol, MedChemExpress), pranlukast (481.50 g/mol, MedChemExpress), dimantine (297.56 g/mol, Biosynth, Staad, Germany), and monobenzone (200.23 g/mol, MedChemExpress) were dissolved in dimethyl sulfoxide (DMSO).

Techniques: Concentration Assay