sulphanilamide Search Results


sulphanilamide  (LGC Standards)
90
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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sulfanilamide  (Thermo Fisher)
94
Thermo Fisher sulfanilamide
Sulfanilamide, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, 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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filters  (Thermo Fisher)
92
Thermo Fisher filters
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.
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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trimethoprim sulfamethoxazole  (Chem Impex International)
95
Chem Impex International trimethoprim sulfamethoxazole
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.
Trimethoprim Sulfamethoxazole, 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  (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 sn  (LGC Standards)
90
LGC Standards sulfanilamide sn
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 Sn, 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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sia enamine  (Enamine Ltd)
99
Enamine Ltd sia enamine
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.
Sia Enamine, supplied by Enamine Ltd, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulfanilamide  (Valiant Co Ltd)
94
Valiant Co Ltd 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 Valiant Co Ltd, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sulphanilamide of drugs  (Wellcome Physiological Research)
90
Wellcome Physiological Research sulphanilamide of drugs
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.
Sulphanilamide Of Drugs, supplied by Wellcome Physiological Research, 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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sulphanilamide (c6h8n2o2s, mw: 172.20 g/mol, ≥99)  (PanReac AppliChem)
90
PanReac AppliChem sulphanilamide (c6h8n2o2s, mw: 172.20 g/mol, ≥99)
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.
Sulphanilamide (C6h8n2o2s, Mw: 172.20 G/Mol, ≥99), supplied by PanReac AppliChem, 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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certified standards for elemental analysis sulphanilamide  (National Institute of Standards and Technology)
90
National Institute of Standards and Technology certified standards for elemental analysis sulphanilamide
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.
Certified Standards For Elemental Analysis Sulphanilamide, supplied by National Institute of Standards and Technology, 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