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prasugrel metabolite  (BOC Sciences)


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    Structured Review

    BOC Sciences prasugrel metabolite
    Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with <t>prasugrel</t> <t>metabolite</t> and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control
    Prasugrel Metabolite, supplied by BOC Sciences, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/prasugrel metabolite/product/BOC Sciences
    Average 93 stars, based on 6 article reviews
    prasugrel metabolite - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions"

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    Journal: Pharmacological Reports

    doi: 10.1007/s43440-023-00447-7

    Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control
    Figure Legend Snippet: Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control

    Techniques Used: Control

    The effect of fentanyl on ADP-induced platelet aggregation in PRP in the absence and presence of  prasugrel metabolite
    Figure Legend Snippet: The effect of fentanyl on ADP-induced platelet aggregation in PRP in the absence and presence of prasugrel metabolite

    Techniques Used: Control, Incubation

    Representative curves of ADP-induced platelet aggregation measured by LTA. The effect of fentanyl on agonist-induced platelet function was measured in PRP, in the absence or presence of 1.3 µM prasugrel metabolite (PM). The example data show platelet response to fentanyl added to PRP with subthreshold concentration of ADP ( A ) or preincubated with PM before stimulation of PRP with 5 µM ADP
    Figure Legend Snippet: Representative curves of ADP-induced platelet aggregation measured by LTA. The effect of fentanyl on agonist-induced platelet function was measured in PRP, in the absence or presence of 1.3 µM prasugrel metabolite (PM). The example data show platelet response to fentanyl added to PRP with subthreshold concentration of ADP ( A ) or preincubated with PM before stimulation of PRP with 5 µM ADP

    Techniques Used: Concentration Assay

    Effect of fentanyl on platelet activation. The influence of 2 or 2000 ng/ml fentanyl on platelet function was measured in blood, PRP or suspensions of isolated platelets in the following models: non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B ), cells stimulated with 2 µM ADP after 15-min preincubation with fentanyl ( C ), and cells stimulated with 10 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D ). Data with normal distribution ( A , B : PRP/platelets, C / D : blood/platelets, D : blood/PRP) are expressed as mean ± SD; otherwise data are presented as median with interquartile range, n = 6‒7. Before statistical analysis, data showing departure from normal distribution were log transformed for normalization. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. the appropriate controls: vehicle ( A ) or ADP ( B ‒ D )
    Figure Legend Snippet: Effect of fentanyl on platelet activation. The influence of 2 or 2000 ng/ml fentanyl on platelet function was measured in blood, PRP or suspensions of isolated platelets in the following models: non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B ), cells stimulated with 2 µM ADP after 15-min preincubation with fentanyl ( C ), and cells stimulated with 10 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D ). Data with normal distribution ( A , B : PRP/platelets, C / D : blood/platelets, D : blood/PRP) are expressed as mean ± SD; otherwise data are presented as median with interquartile range, n = 6‒7. Before statistical analysis, data showing departure from normal distribution were log transformed for normalization. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. the appropriate controls: vehicle ( A ) or ADP ( B ‒ D )

    Techniques Used: Activation Assay, Isolation, Transformation Assay

    Summary of kinetic constants and binding affinities for the interactions of fentanyl and  prasugrel metabolite  with human plasma proteins assayed by SPR
    Figure Legend Snippet: Summary of kinetic constants and binding affinities for the interactions of fentanyl and prasugrel metabolite with human plasma proteins assayed by SPR

    Techniques Used: Binding Assay, Clinical Proteomics

    Representative SPR sensograms showing the interactions of fentanyl or prasugrel metabolite with HSA, α 1 -AGP, ApoA-1, or ApoB-100. The proteins were immobilized to a dextran-coated gold surface. Injection of analyte (10, 20, 40 80 μM fentanyl or 2, 5, 10 μM prasugrel metabolite) produced a signal change that was directly proportional to the mass of bound drug molecules, expressed in resonance units (RU). Further details are given in
    Figure Legend Snippet: Representative SPR sensograms showing the interactions of fentanyl or prasugrel metabolite with HSA, α 1 -AGP, ApoA-1, or ApoB-100. The proteins were immobilized to a dextran-coated gold surface. Injection of analyte (10, 20, 40 80 μM fentanyl or 2, 5, 10 μM prasugrel metabolite) produced a signal change that was directly proportional to the mass of bound drug molecules, expressed in resonance units (RU). Further details are given in

    Techniques Used: Injection, Produced



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    Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with <t>prasugrel</t> <t>metabolite</t> and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control
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    Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: Effect of fentanyl on platelet aggregation in whole blood. The influence of 2 or 2000 ng/ml fentanyl on whole blood platelet aggregation was measured in non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B , C ), and cells stimulated with 5 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D , E ). Data with normal distribution ( A , C ‒ E ) are expressed as mean ± SD, and those with non-normal distribution ( B ) are given as median with interquartile range, n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Control

    The effect of fentanyl on ADP-induced platelet aggregation in PRP in the absence and presence of  prasugrel metabolite

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: The effect of fentanyl on ADP-induced platelet aggregation in PRP in the absence and presence of prasugrel metabolite

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Control, Incubation

    Representative curves of ADP-induced platelet aggregation measured by LTA. The effect of fentanyl on agonist-induced platelet function was measured in PRP, in the absence or presence of 1.3 µM prasugrel metabolite (PM). The example data show platelet response to fentanyl added to PRP with subthreshold concentration of ADP ( A ) or preincubated with PM before stimulation of PRP with 5 µM ADP

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: Representative curves of ADP-induced platelet aggregation measured by LTA. The effect of fentanyl on agonist-induced platelet function was measured in PRP, in the absence or presence of 1.3 µM prasugrel metabolite (PM). The example data show platelet response to fentanyl added to PRP with subthreshold concentration of ADP ( A ) or preincubated with PM before stimulation of PRP with 5 µM ADP

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Concentration Assay

    Effect of fentanyl on platelet activation. The influence of 2 or 2000 ng/ml fentanyl on platelet function was measured in blood, PRP or suspensions of isolated platelets in the following models: non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B ), cells stimulated with 2 µM ADP after 15-min preincubation with fentanyl ( C ), and cells stimulated with 10 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D ). Data with normal distribution ( A , B : PRP/platelets, C / D : blood/platelets, D : blood/PRP) are expressed as mean ± SD; otherwise data are presented as median with interquartile range, n = 6‒7. Before statistical analysis, data showing departure from normal distribution were log transformed for normalization. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. the appropriate controls: vehicle ( A ) or ADP ( B ‒ D )

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: Effect of fentanyl on platelet activation. The influence of 2 or 2000 ng/ml fentanyl on platelet function was measured in blood, PRP or suspensions of isolated platelets in the following models: non-stimulated cells ( A ), cells stimulated with 2 µM ADP in combination with fentanyl ( B ), cells stimulated with 2 µM ADP after 15-min preincubation with fentanyl ( C ), and cells stimulated with 10 µM ADP after 15-min preincubation with prasugrel metabolite and fentanyl ( D ). Data with normal distribution ( A , B : PRP/platelets, C / D : blood/platelets, D : blood/PRP) are expressed as mean ± SD; otherwise data are presented as median with interquartile range, n = 6‒7. Before statistical analysis, data showing departure from normal distribution were log transformed for normalization. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. the appropriate controls: vehicle ( A ) or ADP ( B ‒ D )

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Activation Assay, Isolation, Transformation Assay

    Summary of kinetic constants and binding affinities for the interactions of fentanyl and  prasugrel metabolite  with human plasma proteins assayed by SPR

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: Summary of kinetic constants and binding affinities for the interactions of fentanyl and prasugrel metabolite with human plasma proteins assayed by SPR

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Binding Assay, Clinical Proteomics

    Representative SPR sensograms showing the interactions of fentanyl or prasugrel metabolite with HSA, α 1 -AGP, ApoA-1, or ApoB-100. The proteins were immobilized to a dextran-coated gold surface. Injection of analyte (10, 20, 40 80 μM fentanyl or 2, 5, 10 μM prasugrel metabolite) produced a signal change that was directly proportional to the mass of bound drug molecules, expressed in resonance units (RU). Further details are given in

    Journal: Pharmacological Reports

    Article Title: Interactions of fentanyl with blood platelets and plasma proteins: platelet sensitivity to prasugrel metabolite is not affected by fentanyl under in vitro conditions

    doi: 10.1007/s43440-023-00447-7

    Figure Lengend Snippet: Representative SPR sensograms showing the interactions of fentanyl or prasugrel metabolite with HSA, α 1 -AGP, ApoA-1, or ApoB-100. The proteins were immobilized to a dextran-coated gold surface. Injection of analyte (10, 20, 40 80 μM fentanyl or 2, 5, 10 μM prasugrel metabolite) produced a signal change that was directly proportional to the mass of bound drug molecules, expressed in resonance units (RU). Further details are given in

    Article Snippet: Prasugrel metabolite (R-138727) was obtained from BOC Sciences (Shirley, NY, USA).

    Techniques: Injection, Produced