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  • 99
    Thermo Fisher api 4000 lc ms ms mass spectrometer
    Api 4000 Lc Ms Ms Mass Spectrometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/api 4000 lc ms ms mass spectrometer/product/Thermo Fisher
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    99
    SCIEX api4000 lc ms system
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api4000 Lc Ms System, supplied by SCIEX, used in various techniques. Bioz Stars score: 99/100, based on 26 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/api4000 lc ms system/product/SCIEX
    Average 99 stars, based on 26 article reviews
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    api4000 lc ms system - by Bioz Stars, 2020-08
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    90
    Thermo Fisher api4000 lc ms ms instrument
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api4000 Lc Ms Ms Instrument, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/api4000 lc ms ms instrument/product/Thermo Fisher
    Average 90 stars, based on 13 article reviews
    Price from $9.99 to $1999.99
    api4000 lc ms ms instrument - by Bioz Stars, 2020-08
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    90
    SCIEX sciex api4000 lc ms ms
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Sciex Api4000 Lc Ms Ms, supplied by SCIEX, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sciex api4000 lc ms ms/product/SCIEX
    Average 90 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
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    88
    Agilent technologies ctc agilent 1100 ab sciex api4000 lc ms
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Ctc Agilent 1100 Ab Sciex Api4000 Lc Ms, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Thermo Fisher sciex api 4000 lc ms ms
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Sciex Api 4000 Lc Ms Ms, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sciex api 4000 lc ms ms/product/Thermo Fisher
    Average 85 stars, based on 9 article reviews
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    85
    Thermo Fisher api 4000 lc ms ms triple quadrupole mass spectrometer
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api 4000 Lc Ms Ms Triple Quadrupole Mass Spectrometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    PerkinElmer api 4000 lc ms ms system
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api 4000 Lc Ms Ms System, supplied by PerkinElmer, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/api 4000 lc ms ms system/product/PerkinElmer
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    90
    Charles River Laboratories api 4000 lc ms ms system
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api 4000 Lc Ms Ms System, supplied by Charles River Laboratories, 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/result/api 4000 lc ms ms system/product/Charles River Laboratories
    Average 90 stars, based on 1 article reviews
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    api 4000 lc ms ms system - by Bioz Stars, 2020-08
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    91
    Agilent technologies api 4000 lc ms ms system
    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the <t>API</t> 4000 MS from the m/z 417 thiol dimer.
    Api 4000 Lc Ms Ms System, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/api 4000 lc ms ms system/product/Agilent technologies
    Average 91 stars, based on 1 article reviews
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    Image Search Results


    Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the API 4000 MS from the m/z 417 thiol dimer.

    Journal: International Journal for Parasitology: Drugs and Drug Resistance

    Article Title: TPT sulfonate, a single, oral dose schistosomicidal prodrug: In vivo efficacy, disposition and metabolic profiling

    doi: 10.1016/j.ijpddr.2018.10.004

    Figure Lengend Snippet: Relative ion abundance of TPT sulfonate metabolites from mouse plasma and a mouse hepatocyte digest. MS/MS peak areas are compared for metabolites observed in ( A ) mouse plasma 4 h after 100 mg/kg PO dosing and in ( B ) a mouse hepatocyte incubation after 20 min, using 400 μM TPT sulfonate and 3 × 10 6 cells/m. Solid colors represent metabolites depicted in Fig. 9 ; cross-hatching indicates metabolites differing from those in the figure by two mass units (possibly representing a gain or loss of a double bond) and vertical stripes indicate metabolites of unknown structure. Data were obtained via m/z 56 neutral loss scanning from m/z 100 to 320. The m/z 208 compound is not a metabolite per se , but a decomposition product that forms in the inlet to the API 4000 MS from the m/z 417 thiol dimer.

    Article Snippet: 2.7 Positive ion-mode electrospray tandem MS of TPT sulfonate and its metabolites in mouse plasma and mouse hepatocyte digests The principal fragments of m/z 290 TPT sulfonate observed using an API 4000 LC-MS/MS system (SCIEX, Framingham, MA) (see description under Results) are m/z 234, 135, 120 and 91.

    Techniques: Mass Spectrometry, Incubation