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lcms-2010a mass spectrometer  (Shimadzu Corporation)


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    Shimadzu Corporation lcms-2010a mass spectrometer
    Lcms 2010a Mass Spectrometer, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lcms-2010a/uv+vis+spectrophotomet/pm38604019-50-14-13
    Average 90 stars, based on 1 article reviews
    lcms-2010a mass spectrometer - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Concentration Assay:

    Article Title: Development of a Highly Selective and Sensitive Fluorescent Probe for Imaging RNA Dynamics in Live Cells
    Article Snippet: Mass spectra (MS) were recorded on a Shimadzu LCMS-2010A instrument (Tokyo, Japan) with an ESI or ACPI mass selective detector and high-resolution mass spectra (HRMS) were recorded on a Shimadzu LCMS-IT-TOF (Tokyo, Japan).

    Article Title: Lactic Acid from CO 2 : A Carbon Capture and Utilization Strategy Based on a Biocatalytic Approach
    Article Snippet: In the case of lactic acid, the measurement of concentration was performed with a Shimadzu LCMS-2010A using an ICSep 87H USP L17 (Transgenomic) column.

    Article Title: Design, synthesis and evaluation of N3-substituted quinazolinone derivatives as potential Bloom's Syndrome protein (BLM) helicase inhibitor for sensitization treatment of colorectal cancer.
    Article Snippet: The homologous recombination repair (HRR) pathway is critical for repairing double-strand breaks (DSB).. Inhibition of the HRR pathway is usually considered a promising strategy for anticancer therapy.. The Bloom’s Syndrome Protein (BLM), a DNA helicase, is essential for promoting the HRR pathway.

    Article Title: Structure-guided optimization and mechanistic study of a class of quinazolinone-threonine hybrids as antibacterial ThrRS inhibitors.
    Article Snippet: Aminoacyl-tRNA synthetases (aaRSs) are an attractive class of antibacterial drug targets due to their essential roles in protein translation.. While most traditional aaRS inhibitors target the binding pockets of substrate amino acids and/or ATP, we recently developed a class of novel tRNA-amino acid dual-site inhibitors including inhibitor 3 ((2S,3R)-2-amino-N-((E)-4-(6,7-dichloro-4-oxoquinazolin-3(4H)-yl)but2-en-1-yl)-3-hydroxybutanamide) against threonyl-tRNA synthetase (ThrRS).. Here, the binding modes and structure-activity relationships (SARs) of these inhibitors were analyzed by the crystal structures of Salmonella enterica ThrRS (SeThrRS) in complex with three of them.

    Article Title: Ultrasonic‐assisted preparation of Co 3 O 4 and Eu‐doped Co 3 O 4 nanocatalysts and their application for solvent‐free synthesis of 2‐amino‐4 H ‐benzochromenes under microwave irradiation
    Article Snippet: Funding information Urmia University Co3O4 and Eu-doped Co3O4 nanocatalysts were synthesized through an ultrasonic-assisted solvothermal method and were characterized with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), energy-dispersive X-ray (EDX), and field-emission scanning electron microscopy (FESEM) methods.. Spinel cubic crystalline system for synthesized nanocatalysts was confirmed with XRD, whereas the spherical morphology of Co3O4 changed to nanorods after Eu doping, which was affirmed with FESEM micrographs.. Catalytic performance of the nanomaterials was examined through the synthesis of 2-amino-4H-benzochromenes using aromatic aldehydes, malononitrile, and β-naphthol condensation under solvent-free conditions and microwave irradiation.

    Article Title: Novel pyrimidines as COX-2 selective inhibitors: synthesis, DFT analysis, molecular docking and dynamic simulation studies.
    Article Snippet: Pyrimidine and its derivatives are associated with varieties of biological properties.. Therefore, we herein reported the synthesis of four novel pyrimidines (2, 3, and 4a, b) derivatives.. The structure of these molecules is confirmed by spectroscopic methods such as IR, NMR, and Mass analysis.

    Article Title: A Flavone-Based Long-Wavelength Fluorescent Probe to Detect Biothiols <i>in vitro</i> and <i>in vivo</i>
    Article Snippet: HPLC-MS spectra were recorded on a Shimadzu LCMS-2010A instrument with an ESI mass selective detector.

    Article Title: Development and Phytochemical Characterization of High Polyphenol Red Lettuce with Anti-Diabetic Properties
    Article Snippet: Methanolic extract samples were separated and analyzed with a Shimadzu LCMS-2010A high performance liquid chromatography/electrospray ionization/single quadrupole mass spectrometer.

    Liquid Chromatography with Mass Spectroscopy:

    Article Title: Development of a Highly Selective and Sensitive Fluorescent Probe for Imaging RNA Dynamics in Live Cells
    Article Snippet: Mass spectra (MS) were recorded on a Shimadzu LCMS-2010A instrument (Tokyo, Japan) with an ESI or ACPI mass selective detector and high-resolution mass spectra (HRMS) were recorded on a Shimadzu LCMS-IT-TOF (Tokyo, Japan).

    Article Title: Lactic Acid from CO 2 : A Carbon Capture and Utilization Strategy Based on a Biocatalytic Approach
    Article Snippet: In the case of lactic acid, the measurement of concentration was performed with a Shimadzu LCMS-2010A using an ICSep 87H USP L17 (Transgenomic) column.

    Article Title: Design, synthesis and evaluation of N3-substituted quinazolinone derivatives as potential Bloom's Syndrome protein (BLM) helicase inhibitor for sensitization treatment of colorectal cancer.
    Article Snippet: The homologous recombination repair (HRR) pathway is critical for repairing double-strand breaks (DSB).. Inhibition of the HRR pathway is usually considered a promising strategy for anticancer therapy.. The Bloom’s Syndrome Protein (BLM), a DNA helicase, is essential for promoting the HRR pathway.

    Article Title: Structure-guided optimization and mechanistic study of a class of quinazolinone-threonine hybrids as antibacterial ThrRS inhibitors.
    Article Snippet: Aminoacyl-tRNA synthetases (aaRSs) are an attractive class of antibacterial drug targets due to their essential roles in protein translation.. While most traditional aaRS inhibitors target the binding pockets of substrate amino acids and/or ATP, we recently developed a class of novel tRNA-amino acid dual-site inhibitors including inhibitor 3 ((2S,3R)-2-amino-N-((E)-4-(6,7-dichloro-4-oxoquinazolin-3(4H)-yl)but2-en-1-yl)-3-hydroxybutanamide) against threonyl-tRNA synthetase (ThrRS).. Here, the binding modes and structure-activity relationships (SARs) of these inhibitors were analyzed by the crystal structures of Salmonella enterica ThrRS (SeThrRS) in complex with three of them.

    Article Title: Ultrasonic‐assisted preparation of Co 3 O 4 and Eu‐doped Co 3 O 4 nanocatalysts and their application for solvent‐free synthesis of 2‐amino‐4 H ‐benzochromenes under microwave irradiation
    Article Snippet: Funding information Urmia University Co3O4 and Eu-doped Co3O4 nanocatalysts were synthesized through an ultrasonic-assisted solvothermal method and were characterized with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), energy-dispersive X-ray (EDX), and field-emission scanning electron microscopy (FESEM) methods.. Spinel cubic crystalline system for synthesized nanocatalysts was confirmed with XRD, whereas the spherical morphology of Co3O4 changed to nanorods after Eu doping, which was affirmed with FESEM micrographs.. Catalytic performance of the nanomaterials was examined through the synthesis of 2-amino-4H-benzochromenes using aromatic aldehydes, malononitrile, and β-naphthol condensation under solvent-free conditions and microwave irradiation.

    Article Title: Novel pyrimidines as COX-2 selective inhibitors: synthesis, DFT analysis, molecular docking and dynamic simulation studies.
    Article Snippet: Pyrimidine and its derivatives are associated with varieties of biological properties.. Therefore, we herein reported the synthesis of four novel pyrimidines (2, 3, and 4a, b) derivatives.. The structure of these molecules is confirmed by spectroscopic methods such as IR, NMR, and Mass analysis.

    Article Title: A Flavone-Based Long-Wavelength Fluorescent Probe to Detect Biothiols <i>in vitro</i> and <i>in vivo</i>
    Article Snippet: HPLC-MS spectra were recorded on a Shimadzu LCMS-2010A instrument with an ESI mass selective detector.

    Article Title: Development and Phytochemical Characterization of High Polyphenol Red Lettuce with Anti-Diabetic Properties
    Article Snippet: Methanolic extract samples were separated and analyzed with a Shimadzu LCMS-2010A high performance liquid chromatography/electrospray ionization/single quadrupole mass spectrometer.

    Mass Spectrometry:

    Article Title: Development of a Highly Selective and Sensitive Fluorescent Probe for Imaging RNA Dynamics in Live Cells
    Article Snippet: Mass spectra (MS) were recorded on a Shimadzu LCMS-2010A instrument (Tokyo, Japan) with an ESI or ACPI mass selective detector and high-resolution mass spectra (HRMS) were recorded on a Shimadzu LCMS-IT-TOF (Tokyo, Japan).

    Article Title: Lactic Acid from CO 2 : A Carbon Capture and Utilization Strategy Based on a Biocatalytic Approach
    Article Snippet: In the case of lactic acid, the measurement of concentration was performed with a Shimadzu LCMS-2010A using an ICSep 87H USP L17 (Transgenomic) column.

    Article Title: Design, synthesis and evaluation of N3-substituted quinazolinone derivatives as potential Bloom's Syndrome protein (BLM) helicase inhibitor for sensitization treatment of colorectal cancer.
    Article Snippet: The homologous recombination repair (HRR) pathway is critical for repairing double-strand breaks (DSB).. Inhibition of the HRR pathway is usually considered a promising strategy for anticancer therapy.. The Bloom’s Syndrome Protein (BLM), a DNA helicase, is essential for promoting the HRR pathway.

    Article Title: Structure-guided optimization and mechanistic study of a class of quinazolinone-threonine hybrids as antibacterial ThrRS inhibitors.
    Article Snippet: Aminoacyl-tRNA synthetases (aaRSs) are an attractive class of antibacterial drug targets due to their essential roles in protein translation.. While most traditional aaRS inhibitors target the binding pockets of substrate amino acids and/or ATP, we recently developed a class of novel tRNA-amino acid dual-site inhibitors including inhibitor 3 ((2S,3R)-2-amino-N-((E)-4-(6,7-dichloro-4-oxoquinazolin-3(4H)-yl)but2-en-1-yl)-3-hydroxybutanamide) against threonyl-tRNA synthetase (ThrRS).. Here, the binding modes and structure-activity relationships (SARs) of these inhibitors were analyzed by the crystal structures of Salmonella enterica ThrRS (SeThrRS) in complex with three of them.

    Article Title: Ultrasonic‐assisted preparation of Co 3 O 4 and Eu‐doped Co 3 O 4 nanocatalysts and their application for solvent‐free synthesis of 2‐amino‐4 H ‐benzochromenes under microwave irradiation
    Article Snippet: Funding information Urmia University Co3O4 and Eu-doped Co3O4 nanocatalysts were synthesized through an ultrasonic-assisted solvothermal method and were characterized with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), energy-dispersive X-ray (EDX), and field-emission scanning electron microscopy (FESEM) methods.. Spinel cubic crystalline system for synthesized nanocatalysts was confirmed with XRD, whereas the spherical morphology of Co3O4 changed to nanorods after Eu doping, which was affirmed with FESEM micrographs.. Catalytic performance of the nanomaterials was examined through the synthesis of 2-amino-4H-benzochromenes using aromatic aldehydes, malononitrile, and β-naphthol condensation under solvent-free conditions and microwave irradiation.

    Article Title: Novel pyrimidines as COX-2 selective inhibitors: synthesis, DFT analysis, molecular docking and dynamic simulation studies.
    Article Snippet: Pyrimidine and its derivatives are associated with varieties of biological properties.. Therefore, we herein reported the synthesis of four novel pyrimidines (2, 3, and 4a, b) derivatives.. The structure of these molecules is confirmed by spectroscopic methods such as IR, NMR, and Mass analysis.

    Article Title: A Flavone-Based Long-Wavelength Fluorescent Probe to Detect Biothiols <i>in vitro</i> and <i>in vivo</i>
    Article Snippet: HPLC-MS spectra were recorded on a Shimadzu LCMS-2010A instrument with an ESI mass selective detector.

    Article Title: Development and Phytochemical Characterization of High Polyphenol Red Lettuce with Anti-Diabetic Properties
    Article Snippet: Methanolic extract samples were separated and analyzed with a Shimadzu LCMS-2010A high performance liquid chromatography/electrospray ionization/single quadrupole mass spectrometer.

    High Performance Liquid Chromatography:

    Article Title: Development of a Highly Selective and Sensitive Fluorescent Probe for Imaging RNA Dynamics in Live Cells
    Article Snippet: Mass spectra (MS) were recorded on a Shimadzu LCMS-2010A instrument (Tokyo, Japan) with an ESI or ACPI mass selective detector and high-resolution mass spectra (HRMS) were recorded on a Shimadzu LCMS-IT-TOF (Tokyo, Japan).

    Article Title: Lactic Acid from CO 2 : A Carbon Capture and Utilization Strategy Based on a Biocatalytic Approach
    Article Snippet: In the case of lactic acid, the measurement of concentration was performed with a Shimadzu LCMS-2010A using an ICSep 87H USP L17 (Transgenomic) column.

    Article Title: Design, synthesis and evaluation of N3-substituted quinazolinone derivatives as potential Bloom's Syndrome protein (BLM) helicase inhibitor for sensitization treatment of colorectal cancer.
    Article Snippet: The homologous recombination repair (HRR) pathway is critical for repairing double-strand breaks (DSB).. Inhibition of the HRR pathway is usually considered a promising strategy for anticancer therapy.. The Bloom’s Syndrome Protein (BLM), a DNA helicase, is essential for promoting the HRR pathway.

    Article Title: Structure-guided optimization and mechanistic study of a class of quinazolinone-threonine hybrids as antibacterial ThrRS inhibitors.
    Article Snippet: Aminoacyl-tRNA synthetases (aaRSs) are an attractive class of antibacterial drug targets due to their essential roles in protein translation.. While most traditional aaRS inhibitors target the binding pockets of substrate amino acids and/or ATP, we recently developed a class of novel tRNA-amino acid dual-site inhibitors including inhibitor 3 ((2S,3R)-2-amino-N-((E)-4-(6,7-dichloro-4-oxoquinazolin-3(4H)-yl)but2-en-1-yl)-3-hydroxybutanamide) against threonyl-tRNA synthetase (ThrRS).. Here, the binding modes and structure-activity relationships (SARs) of these inhibitors were analyzed by the crystal structures of Salmonella enterica ThrRS (SeThrRS) in complex with three of them.

    Article Title: Ultrasonic‐assisted preparation of Co 3 O 4 and Eu‐doped Co 3 O 4 nanocatalysts and their application for solvent‐free synthesis of 2‐amino‐4 H ‐benzochromenes under microwave irradiation
    Article Snippet: Funding information Urmia University Co3O4 and Eu-doped Co3O4 nanocatalysts were synthesized through an ultrasonic-assisted solvothermal method and were characterized with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), energy-dispersive X-ray (EDX), and field-emission scanning electron microscopy (FESEM) methods.. Spinel cubic crystalline system for synthesized nanocatalysts was confirmed with XRD, whereas the spherical morphology of Co3O4 changed to nanorods after Eu doping, which was affirmed with FESEM micrographs.. Catalytic performance of the nanomaterials was examined through the synthesis of 2-amino-4H-benzochromenes using aromatic aldehydes, malononitrile, and β-naphthol condensation under solvent-free conditions and microwave irradiation.

    Article Title: Novel pyrimidines as COX-2 selective inhibitors: synthesis, DFT analysis, molecular docking and dynamic simulation studies.
    Article Snippet: Pyrimidine and its derivatives are associated with varieties of biological properties.. Therefore, we herein reported the synthesis of four novel pyrimidines (2, 3, and 4a, b) derivatives.. The structure of these molecules is confirmed by spectroscopic methods such as IR, NMR, and Mass analysis.

    Article Title: A Flavone-Based Long-Wavelength Fluorescent Probe to Detect Biothiols <i>in vitro</i> and <i>in vivo</i>
    Article Snippet: HPLC-MS spectra were recorded on a Shimadzu LCMS-2010A instrument with an ESI mass selective detector.

    Article Title: Development and Phytochemical Characterization of High Polyphenol Red Lettuce with Anti-Diabetic Properties
    Article Snippet: Methanolic extract samples were separated and analyzed with a Shimadzu LCMS-2010A high performance liquid chromatography/electrospray ionization/single quadrupole mass spectrometer.

    Chromatography:

    Article Title: Development of a Highly Selective and Sensitive Fluorescent Probe for Imaging RNA Dynamics in Live Cells
    Article Snippet: Mass spectra (MS) were recorded on a Shimadzu LCMS-2010A instrument (Tokyo, Japan) with an ESI or ACPI mass selective detector and high-resolution mass spectra (HRMS) were recorded on a Shimadzu LCMS-IT-TOF (Tokyo, Japan).

    Article Title: Lactic Acid from CO 2 : A Carbon Capture and Utilization Strategy Based on a Biocatalytic Approach
    Article Snippet: In the case of lactic acid, the measurement of concentration was performed with a Shimadzu LCMS-2010A using an ICSep 87H USP L17 (Transgenomic) column.

    Article Title: Design, synthesis and evaluation of N3-substituted quinazolinone derivatives as potential Bloom's Syndrome protein (BLM) helicase inhibitor for sensitization treatment of colorectal cancer.
    Article Snippet: The homologous recombination repair (HRR) pathway is critical for repairing double-strand breaks (DSB).. Inhibition of the HRR pathway is usually considered a promising strategy for anticancer therapy.. The Bloom’s Syndrome Protein (BLM), a DNA helicase, is essential for promoting the HRR pathway.

    Article Title: Structure-guided optimization and mechanistic study of a class of quinazolinone-threonine hybrids as antibacterial ThrRS inhibitors.
    Article Snippet: Aminoacyl-tRNA synthetases (aaRSs) are an attractive class of antibacterial drug targets due to their essential roles in protein translation.. While most traditional aaRS inhibitors target the binding pockets of substrate amino acids and/or ATP, we recently developed a class of novel tRNA-amino acid dual-site inhibitors including inhibitor 3 ((2S,3R)-2-amino-N-((E)-4-(6,7-dichloro-4-oxoquinazolin-3(4H)-yl)but2-en-1-yl)-3-hydroxybutanamide) against threonyl-tRNA synthetase (ThrRS).. Here, the binding modes and structure-activity relationships (SARs) of these inhibitors were analyzed by the crystal structures of Salmonella enterica ThrRS (SeThrRS) in complex with three of them.

    Article Title: Ultrasonic‐assisted preparation of Co 3 O 4 and Eu‐doped Co 3 O 4 nanocatalysts and their application for solvent‐free synthesis of 2‐amino‐4 H ‐benzochromenes under microwave irradiation
    Article Snippet: Funding information Urmia University Co3O4 and Eu-doped Co3O4 nanocatalysts were synthesized through an ultrasonic-assisted solvothermal method and were characterized with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), energy-dispersive X-ray (EDX), and field-emission scanning electron microscopy (FESEM) methods.. Spinel cubic crystalline system for synthesized nanocatalysts was confirmed with XRD, whereas the spherical morphology of Co3O4 changed to nanorods after Eu doping, which was affirmed with FESEM micrographs.. Catalytic performance of the nanomaterials was examined through the synthesis of 2-amino-4H-benzochromenes using aromatic aldehydes, malononitrile, and β-naphthol condensation under solvent-free conditions and microwave irradiation.

    Article Title: Novel pyrimidines as COX-2 selective inhibitors: synthesis, DFT analysis, molecular docking and dynamic simulation studies.
    Article Snippet: Pyrimidine and its derivatives are associated with varieties of biological properties.. Therefore, we herein reported the synthesis of four novel pyrimidines (2, 3, and 4a, b) derivatives.. The structure of these molecules is confirmed by spectroscopic methods such as IR, NMR, and Mass analysis.

    Article Title: A Flavone-Based Long-Wavelength Fluorescent Probe to Detect Biothiols <i>in vitro</i> and <i>in vivo</i>
    Article Snippet: HPLC-MS spectra were recorded on a Shimadzu LCMS-2010A instrument with an ESI mass selective detector.

    Article Title: Development and Phytochemical Characterization of High Polyphenol Red Lettuce with Anti-Diabetic Properties
    Article Snippet: Methanolic extract samples were separated and analyzed with a Shimadzu LCMS-2010A high performance liquid chromatography/electrospray ionization/single quadrupole mass spectrometer.



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