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1 2 3 4 tetrahydro 6 nitro 2 3 dioxo benzo  (Tocris)


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    Structured Review

    Tocris 1 2 3 4 tetrahydro 6 nitro 2 3 dioxo benzo
    1 2 3 4 Tetrahydro 6 Nitro 2 3 Dioxo Benzo, supplied by Tocris, used in various techniques. Bioz Stars score: 96/100, based on 1989 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nmda+receptor+blocker+cpp/NBQX/pmc04044435-94-7-18
    Average 96 stars, based on 1989 article reviews
    1 2 3 4 tetrahydro 6 nitro 2 3 dioxo benzo - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Rod photoreceptors control the ON vs OFF polarity of cone-signaling neurons.
    Article Snippet: .. AMPA and kainite glutamate receptor antagonists, 6- cyano-7-nitroquinoxaline-2,3-dione (CNQX) (15 μM, Tocris) and 2,3-Dioxo-6-nitro-1,2,3,4tetrahydrobenzo[f]quinoxaline-7-sulfonamide (NBQX) (10 μM, Tocris), were bath applied to block photoreceptor - horizontal cell transmission. .. To block gap junction, meclofenamic acid (MFA) (50-100 μM, Sigma) was used.

    Article Title: Ozanimod and other sphingosine-1-phosphate receptor 1 modulators normalize neuropathic injury-enhanced inhibition of central lateral amygdala neurons expressing corticotropin-releasing hormone.
    Article Snippet: For sEPSC recordings, SR 95531 19 hydrobromide (GABAzine; Tocris, Bristol, UK; 10μM) was added to the ACSF to block 20 GABAergic (inhibitory) inputs. .. For sIPSC recordings, 3-(2-Carboxypiperazin-4-yl) propyl-1-21 phosphonicacid (CPP; Tocris, Bristol, UK; 5μM) and 2,3-dihydroxy-6-nitro-7-sulphamoyl-22 benzo(F)quinoxaline (NBQX; Tocris, Bristol, UK; 10 μM) were added to the ACSF to block N-23 methyl-d-aspartic acid (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid 24 (AMPA) glutamatergic (excitatory) inputs, respectively. ..

    Transmission Assay:

    Article Title: Rod photoreceptors control the ON vs OFF polarity of cone-signaling neurons.
    Article Snippet: .. AMPA and kainite glutamate receptor antagonists, 6- cyano-7-nitroquinoxaline-2,3-dione (CNQX) (15 μM, Tocris) and 2,3-Dioxo-6-nitro-1,2,3,4tetrahydrobenzo[f]quinoxaline-7-sulfonamide (NBQX) (10 μM, Tocris), were bath applied to block photoreceptor - horizontal cell transmission. .. To block gap junction, meclofenamic acid (MFA) (50-100 μM, Sigma) was used.

    other:

    Article Title: Enrichment experience improves hippocampal sparse coding via inhibitory circuit plasticity
    Article Snippet: Stock solutions of NBQX (Tocris Bioscience, 10 mM), D-AP5 (Tocris Bioscience, 25 mM), Gabazine (SR 95531 hydrobromide, Sigma-Aldrich, 10 mM) and Tetrodotoxin (TTX, Alomone Labs, 1 mM) were dissolved in water.

    Article Title: Functional Ca 2+ -permeable AMPA receptors in hippocampal astrocytes mediate calcium signaling in vitro.
    Article Snippet: The drugs applied during the different recordings included alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) at 20 μM (Alomone, Cat No. A-267), 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline (NBQX) at 50 μM (Tocris, Cat. No. 1044), cyclothiazide (CTZ) at 10 μM (Tocris, Cat. No. 0713), ionomycin at 3 μM (SigmaAldrich Merck, Cat. No. I0634), N-acetylspermine (NASPM) at 50 μM (Tocris, Cat. No. 2766), adenosine triphosphate (ATP) at 10 μM (Sigma-Aldrich Merck, Cat. No. A1852-1VL), and A438079 hydrochloride hydrate at 10 μM (Sigma-Aldrich Merck, Cat. No. A9736).



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    Image Search Results


    a Schematics of cerebellar circuit. b UMAP embedding showing normalized expression of gene involved in mGluR1 signaling cascade. c Same as in b for AMPA and NMDA receptors. d Same as in b for genes involved in mGluR2/3 signaling cascade. e Example spiking responses in different UBCs to a burst of MF input (20 stimuli at 100 Hz). f Instantaneous firing rate for the same cells.

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Schematics of cerebellar circuit. b UMAP embedding showing normalized expression of gene involved in mGluR1 signaling cascade. c Same as in b for AMPA and NMDA receptors. d Same as in b for genes involved in mGluR2/3 signaling cascade. e Example spiking responses in different UBCs to a burst of MF input (20 stimuli at 100 Hz). f Instantaneous firing rate for the same cells.

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 µM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 µM NBQX), NMDA receptor blocker (2 µM R-CPP), mGluR2/3 antagonist (1 µM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 µM R59949, MilliporeSigma, St. Louis, MO)

    Techniques: Expressing

    a Examples of instantaneous firing rate from on-cell recordings before (black) and after (gray) the application of AMPA/NMDA receptor antagonist (gray bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. b Summary of evoked spiking (20 × 100 Hz) and the effect of AMPA/NMDA receptor antagonist (normalized to baseline, mean ± sem, n = 5). c Examples of instantaneous firing rate from on-cell recordings before (black) and after (red) the application of an mGluR1 antagonist (red bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. d Summary of evoked spiking (20 × 100 Hz) and the effect of an mGluR1 antagonist (normalized to baseline, mean±sem, n = 5). e Example of instantaneous firing rate before and after 20 minutes of DGK inhibitor II wash-in. f Summary of half-decay time of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean ± sem, n = 6). g Summary of peak amplitude of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean±sem, n = 6).

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Examples of instantaneous firing rate from on-cell recordings before (black) and after (gray) the application of AMPA/NMDA receptor antagonist (gray bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. b Summary of evoked spiking (20 × 100 Hz) and the effect of AMPA/NMDA receptor antagonist (normalized to baseline, mean ± sem, n = 5). c Examples of instantaneous firing rate from on-cell recordings before (black) and after (red) the application of an mGluR1 antagonist (red bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. d Summary of evoked spiking (20 × 100 Hz) and the effect of an mGluR1 antagonist (normalized to baseline, mean±sem, n = 5). e Example of instantaneous firing rate before and after 20 minutes of DGK inhibitor II wash-in. f Summary of half-decay time of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean ± sem, n = 6). g Summary of peak amplitude of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean±sem, n = 6).

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 µM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 µM NBQX), NMDA receptor blocker (2 µM R-CPP), mGluR2/3 antagonist (1 µM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 µM R59949, MilliporeSigma, St. Louis, MO)

    Techniques:

    a Sample cell-attached recording (top) instantaneous firing rate (middle) and synaptic current measured with whole-cell voltage clamp (bottom) in a cell with fast response. b Same as in a but for a cell with intermediate speed response. c Same as in a but for a cell with clear biphasic synaptic current (bottom). d Same as in a but for a cell with slow biphasic response. e Same as in a but for a cell with only a pause in firing. f Half-decay times of firing rates vs. half-decay times of currents and linear fit on a log-log plot ( R adj 2 = 0.91, slope = 0.88, intercept = −0.22, n = 17). g Peak firing rate vs. peak current amplitude and linear fit on a log-log plot ( R adj 2 = 0.69, slope = 0.71, intercept = −0.65, n = 17). h Pause duration vs. amplitude of the current at stimulation offset, and linear fit with log 10 response variable (black, R adj 2 = 0.44, slope = 0.01, intercept = −0.42, n = 20). i Heatmap of peak normalized mGluR1-mediated current ( n = 10). j Heatmap of peak normalized mGluR2/3-mediated current ( n = 7). k Average synaptic response before (black), after (red) mGluR1 antagonist, and after AMPA/NMDA receptor antagonist wash-ins (gray). Each trace is an average of 8 trials. l Average synaptic response before (top, black) and after (top, blue) mGluR2/3 antagonist wash-in, and their difference (bottom, black). Each trace is an average of 8 trials.

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Sample cell-attached recording (top) instantaneous firing rate (middle) and synaptic current measured with whole-cell voltage clamp (bottom) in a cell with fast response. b Same as in a but for a cell with intermediate speed response. c Same as in a but for a cell with clear biphasic synaptic current (bottom). d Same as in a but for a cell with slow biphasic response. e Same as in a but for a cell with only a pause in firing. f Half-decay times of firing rates vs. half-decay times of currents and linear fit on a log-log plot ( R adj 2 = 0.91, slope = 0.88, intercept = −0.22, n = 17). g Peak firing rate vs. peak current amplitude and linear fit on a log-log plot ( R adj 2 = 0.69, slope = 0.71, intercept = −0.65, n = 17). h Pause duration vs. amplitude of the current at stimulation offset, and linear fit with log 10 response variable (black, R adj 2 = 0.44, slope = 0.01, intercept = −0.42, n = 20). i Heatmap of peak normalized mGluR1-mediated current ( n = 10). j Heatmap of peak normalized mGluR2/3-mediated current ( n = 7). k Average synaptic response before (black), after (red) mGluR1 antagonist, and after AMPA/NMDA receptor antagonist wash-ins (gray). Each trace is an average of 8 trials. l Average synaptic response before (top, black) and after (top, blue) mGluR2/3 antagonist wash-in, and their difference (bottom, black). Each trace is an average of 8 trials.

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 µM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 µM NBQX), NMDA receptor blocker (2 µM R-CPP), mGluR2/3 antagonist (1 µM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 µM R59949, MilliporeSigma, St. Louis, MO)

    Techniques:

    a Schematics of cerebellar circuit. b UMAP embedding showing normalized expression of gene involved in mGluR1 signaling cascade. c Same as in b for AMPA and NMDA receptors. d Same as in b for genes involved in mGluR2/3 signaling cascade. e Example spiking responses in different UBCs to a burst of MF input (20 stimuli at 100 Hz). f Instantaneous firing rate for the same cells.

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Schematics of cerebellar circuit. b UMAP embedding showing normalized expression of gene involved in mGluR1 signaling cascade. c Same as in b for AMPA and NMDA receptors. d Same as in b for genes involved in mGluR2/3 signaling cascade. e Example spiking responses in different UBCs to a burst of MF input (20 stimuli at 100 Hz). f Instantaneous firing rate for the same cells.

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 μM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 μM NBQX), NMDA receptor blocker (2 μM R-CPP), mGluR2/3 antagonist (1 μM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 μM R59949, MilliporeSigma, St. Louis, MO)

    Techniques: Expressing

    a Examples of instantaneous firing rate from on-cell recordings before (black) and after (gray) the application of AMPA/NMDA receptor antagonist (gray bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. b Summary of evoked spiking (20 × 100 Hz) and the effect of AMPA/NMDA receptor antagonist (normalized to baseline, mean ± sem, n = 5). c Examples of instantaneous firing rate from on-cell recordings before (black) and after (red) the application of an mGluR1 antagonist (red bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. d Summary of evoked spiking (20 × 100 Hz) and the effect of an mGluR1 antagonist (normalized to baseline, mean±sem, n = 5). e Example of instantaneous firing rate before and after 20 minutes of DGK inhibitor II wash-in. f Summary of half-decay time of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean ± sem, n = 6). g Summary of peak amplitude of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean±sem, n = 6).

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Examples of instantaneous firing rate from on-cell recordings before (black) and after (gray) the application of AMPA/NMDA receptor antagonist (gray bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. b Summary of evoked spiking (20 × 100 Hz) and the effect of AMPA/NMDA receptor antagonist (normalized to baseline, mean ± sem, n = 5). c Examples of instantaneous firing rate from on-cell recordings before (black) and after (red) the application of an mGluR1 antagonist (red bar) in a fast (left) and a slow (right) UBC. Each trace is an average of 8 trials. d Summary of evoked spiking (20 × 100 Hz) and the effect of an mGluR1 antagonist (normalized to baseline, mean±sem, n = 5). e Example of instantaneous firing rate before and after 20 minutes of DGK inhibitor II wash-in. f Summary of half-decay time of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean ± sem, n = 6). g Summary of peak amplitude of instantaneous firing rate response with DGK inhibitor II (normalized to baseline, mean±sem, n = 6).

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 μM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 μM NBQX), NMDA receptor blocker (2 μM R-CPP), mGluR2/3 antagonist (1 μM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 μM R59949, MilliporeSigma, St. Louis, MO)

    Techniques:

    a Sample cell-attached recording (top) instantaneous firing rate (middle) and synaptic current measured with whole-cell voltage clamp (bottom) in a cell with fast response. b Same as in a but for a cell with intermediate speed response. c Same as in a but for a cell with clear biphasic synaptic current (bottom). d Same as in a but for a cell with slow biphasic response. e Same as in a but for a cell with only a pause in firing. f Half-decay times of firing rates vs. half-decay times of currents and linear fit on a log-log plot ( R adj 2 = 0.91, slope = 0.88, intercept = −0.22, n = 17). g Peak firing rate vs. peak current amplitude and linear fit on a log-log plot ( R adj 2 = 0.69, slope = 0.71, intercept = −0.65, n = 17). h Pause duration vs. amplitude of the current at stimulation offset, and linear fit with log 10 response variable (black, R adj 2 = 0.44, slope = 0.01, intercept = −0.42, n = 20). i Heatmap of peak normalized mGluR1-mediated current ( n = 10). j Heatmap of peak normalized mGluR2/3-mediated current ( n = 7). k Average synaptic response before (black), after (red) mGluR1 antagonist, and after AMPA/NMDA receptor antagonist wash-ins (gray). Each trace is an average of 8 trials. l Average synaptic response before (top, black) and after (top, blue) mGluR2/3 antagonist wash-in, and their difference (bottom, black). Each trace is an average of 8 trials.

    Journal: Nature Communications

    Article Title: Graded heterogeneity of metabotropic signaling underlies a continuum of cell-intrinsic temporal responses in unipolar brush cells

    doi: 10.1038/s41467-021-22893-8

    Figure Lengend Snippet: a Sample cell-attached recording (top) instantaneous firing rate (middle) and synaptic current measured with whole-cell voltage clamp (bottom) in a cell with fast response. b Same as in a but for a cell with intermediate speed response. c Same as in a but for a cell with clear biphasic synaptic current (bottom). d Same as in a but for a cell with slow biphasic response. e Same as in a but for a cell with only a pause in firing. f Half-decay times of firing rates vs. half-decay times of currents and linear fit on a log-log plot ( R adj 2 = 0.91, slope = 0.88, intercept = −0.22, n = 17). g Peak firing rate vs. peak current amplitude and linear fit on a log-log plot ( R adj 2 = 0.69, slope = 0.71, intercept = −0.65, n = 17). h Pause duration vs. amplitude of the current at stimulation offset, and linear fit with log 10 response variable (black, R adj 2 = 0.44, slope = 0.01, intercept = −0.42, n = 20). i Heatmap of peak normalized mGluR1-mediated current ( n = 10). j Heatmap of peak normalized mGluR2/3-mediated current ( n = 7). k Average synaptic response before (black), after (red) mGluR1 antagonist, and after AMPA/NMDA receptor antagonist wash-ins (gray). Each trace is an average of 8 trials. l Average synaptic response before (top, black) and after (top, blue) mGluR2/3 antagonist wash-in, and their difference (bottom, black). Each trace is an average of 8 trials.

    Article Snippet: Sequential drug wash-ins were performed using a computer-controlled solenoid manifold system (ValveLink 8.2, Automate Scientific, Inc., Berkeley, CA) with a flow rate of 1 to 2 mL/min, where indicated, with mGluR1 antagonist (100 μM LY357385, Tocris Bio-Techne, Minneapolis, MN), AMPA receptor blocker (5 μM NBQX), NMDA receptor blocker (2 μM R-CPP), mGluR2/3 antagonist (1 μM LY341495, Tocris Bio-Techne, Minneapolis, MN) and DGK inhibitor II (100 μM R59949, MilliporeSigma, St. Louis, MO)

    Techniques: