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kt5823  (Alomone Labs)


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    Alomone Labs kt5823
    Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and <t>KT5823</t> (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).
    Kt5823, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/k-250/pmc12552588-112-14-30?v=Alomone+Labs
    Average 93 stars, based on 5 article reviews
    kt5823 - by Bioz Stars, 2026-07
    93/100 stars

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    1) Product Images from "Tectorigenin induces vasorelaxation in porcine coronary arteries through activation of Kv channels and oestrogen receptor modulation"

    Article Title: Tectorigenin induces vasorelaxation in porcine coronary arteries through activation of Kv channels and oestrogen receptor modulation

    Journal: Scientific Reports

    doi: 10.1038/s41598-025-20988-6

    Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and KT5823 (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).
    Figure Legend Snippet: Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and KT5823 (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).

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    kt5823  (Alomone Labs)
    93
    Alomone Labs kt5823
    Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and <t>KT5823</t> (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).
    Kt5823, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/k-250/pmc12552588-112-14-30?v=Alomone+Labs
    Average 93 stars, based on 1 article reviews
    kt5823 - by Bioz Stars, 2026-07
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    Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and KT5823 (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).

    Journal: Scientific Reports

    Article Title: Tectorigenin induces vasorelaxation in porcine coronary arteries through activation of Kv channels and oestrogen receptor modulation

    doi: 10.1038/s41598-025-20988-6

    Figure Lengend Snippet: Effects of neural and cyclic nucleotide pathway inhibitors on tectorigenin-induced relaxation in porcine coronary arteries pre-contracted with 100 nM U46619. ( A ) Tetrodotoxin (TTX, 1 µM) and ω-conotoxin GVIA (CTX, 1 µM) had no significant effect on the relaxation induced by 30 µM tectorigenin ( p > 0.05, n = 4). ( B ) Pretreatment with rolipram (1 µM, a selective phosphodiesterase-4 inhibitor) or vardenafil (1 µM, a selective phosphodiesterase-5 inhibitor) did not significantly alter tectorigenin-induced vasorelaxation ( p > 0.05, n = 4). ( C ) Inhibitors of the nitric oxide and cyclic nucleotide pathways, including Nω-nitro-L-arginine (L-NNA, 100 µM), KT5720 (1 µM, a PKA inhibitor), and KT5823 (1 µM, a PKG inhibitor), also did not significantly affect the relaxant response to tectorigenin ( p > 0.05, n = 4). Data are expressed as mean ± standard error of the mean (SEM) from four independent hearts. U46619 plateau (normalised to 60 mM KCl) was similar across groups ( p > 0.05; Supplementary Table 2).

    Article Snippet: For experimental assays, a range of pharmacological agents was utilised, including U46619, apamin, KT5720, KT5823, and L-NNA (Sigma-Aldrich, MO, USA); rolipram, vardenafil, and TEA (Santa Cruz Biotechnology, CA, USA); IbTX (Alomone Labs, Jerusalem, Israel); glibenclamide (Research Biochemicals International, MA, USA); TTX and 4-AP (Tocris Bioscience, Bristol, UK); CTX (Bachem, Bubendorf, Switzerland); and charybdotoxin, methyl-piperidino-pyrazole (MPP), and PHTPP (Cayman Chemical, MI, USA).

    Techniques: