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Reagents

A substance which is used as a chemical reaction or it is a test reactions occurs. A reagents is to measure the chemical substance is present or not because reagents is the components or a mixture. A chemical reagents works like a detectives which charged and point out the other substance in chemical reactions. For making a reagents the equal number of volumes solutions A and B use immediately and then it is used as a reagents.1.5g of ferric chloride and 2.0g of potassium thiocynate in 100 ml water to dissolve after that make saturated solution in 50% ethnol.

The reagents take action when solvents involved in the reaction which are usually called reactants but catalysts are not consumed with the reactions hence they are not reactants. Iodine is not soluble in water therefore the iodine reagents is made in dissolving the water with a helps of potassium iodide.

  • Z-VRPR-FMK

    Biovision | Z-VRPR-FMK | B1238

    Z-VRPR-FMK is selective and irreversible MALT-1 (Mucosa-associated lymphoid tissue lymphoma translocation protein 1) inhibitor that inhibits NF- κB dependent gene expression affecting the growth,...

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  • Z-VEID-FMK

    Biovision | Z-VEID-FMK | 1146

    VEID is the specific recognition sequence for caspase-6/Mch2. The inhibitor is designed as a methyl ester to facilitate cell permeability. (CAUTION: If the intended use is on purified or recombinant...

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  • Z-VDVAD-FMK

    Biovision | Z-VDVAD-FMK | 1142

    A synthetic peptide that irreversibly inhibits activity of caspase-2. The inhibitor is designed as a methyl ester to facilitate cell permeability. The product can be used for both in vitro and in...

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  • Z-VAD-FMK

    Biovision | Z-VAD-FMK | 1140

    A synthetic peptide that irreversibly inhibits activity of caspase family proteases and blocks apoptosis. The inhibitor is designed as a methyl ester to facilitate cell permeability. The product can...

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  • ZnAF-2, 6-Iso

    Biovision | ZnAF-2, 6-Iso | 2756

    ZnAF-2, 6-iso-, is a cell-impermeable compound that acts as a high-affinity Zn²⁺-specific fluorescent probe (Kd = 2.7 nM). It shows low basal fluorescence and the fluorescence intensity increases...

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  • ZM 447439

    Biovision | ZM 447439 | 2018

    Cell-permeable. A selective, ATP-competitive inhibitor of Aurora B kinase in vitro (IC₅₀ values are 50 nM, 250 nM and 1 μM for Aurora B, C and A kinases respectively). Selective over a range of other...

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  • Z-LEVD-FMK

    Biovision | Z-LEVD-FMK | 1144

    A synthetic peptide that irreversibly inhibits activity of LEVD-dependent caspases (e.g., caspase-4). The inhibitor is designed as a methyl ester to facilitate cell permeability. The product can be...

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  • Z-LEHD-FMK

    Biovision | Z-LEHD-FMK | 1149

    A synthetic peptide that irreversibly inhibits caspase-9 and related caspase activity. The inhibitor is designed as a methyl ester to facilitate cell permeability. (CAUTION: If the intended use is on...

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  • Zinpyr-1

    Biovision | Zinpyr-1 | 2754

    Zinpyr-1 is a membrane-permeable fluorophore suitable for the fluorometric detection of free Zn²⁺. In living cells, Zinpyr-1 mainly stains the Golgi or a Golgi-associated vesicle.Zinpyr-1 is a...

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  • Z-FA-FMK

    Biovision | Z-FA-FMK | 1986

    Cell-permeable. A useful negative control for FMK-labeled caspase inhibitors. Also, an irreversible inhibitor of cathepsins B, L, and S, and likely cathepsin H, as well as cruzain and papain.Z-FA-FMK...

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  • Z-ATAD-FMK

    Biovision | Z-ATAD-FMK | 1152

    A synthetic peptide that irreversibly inhibits caspase-12 and related caspase activity. The inhibitor is designed as a methyl ester to facilitate cell permeability. (CAUTION: If the intended use is...

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  • Z-AEVD-FMK

    Biovision | Z-AEVD-FMK | B1162

    Z-AEVD-FMK is a synthetic peptide inhibitor that inhibits caspase-10 and related caspase activity. FMK inhibitors are irreversible and non-toxic, and can be used in both in vivo and in vitro studies...

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  • YM201636

    Biovision | YM201636 | 2045

    Cell-permeable. YM-201636 is a selective inhibitor of phosphoinositide kinase (PIK) PIKfyve (IC50 = 33 nM). It inhibits p110α at higher concentration (IC50 = 3 µM). It reversibly impairs endosomal...

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  • YM155

    Biovision | YM155 | 2310

    YM155 is a novel small molecule survivin suppressant; suppresses the expression of surviving and induces apoptosis in PC-3 and PPC-1 human HRPC cell lines at 10 nmol/L.YM155 is a novel small molecule...

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  • YC-1

    Biovision | YC-1 | 2061

    Cell-permeable. A nitric oxide (NO) independent, superoxide-sensitive soluble guanylyl cyclase (sGC) activator (EC₅₀ = 18 µM). Induces concentration-dependent increase in cGMP levels in cultured...

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  • XL765

    Biovision | XL765 | 2551

    XL765 is a dual inhibitor of mTOR/PI3K with potential anticancer activities. XL765 inhibits both PI3 kinase and mTOR kinase, which may result in tumor cell apoptosis and growth inhibition in...

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  • XL-647

    Biovision | XL-647 | B2204

    XL-647 is an orally bioavailable small-molecule receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic activity. It binds to and inhibits several receptor tyrosine kinases that play...

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  • XL-228

    Biovision | XL-228 | 2632

    XL228 is a potent Tyrosine Kinase Inhibitor (TKI). It displays activity against IGF1R, the Aurora kinases, FGFR1-3, ABL and SRC family kinases.XL228 is a potent Tyrosine Kinase Inhibitor (TKI). It...

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  • XL-147

    Biovision | XL-147 | 9401

    XL-147 is an ATP-competitive, highly selective, and reversible pan-class I phosphoinositide 3-kinase (PI3K) inhibitor. It inhibits PI3K p110α, -β, -γ, and -δ isoforms, with IC₅₀ values of 48, 617,...

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  • Xestospongin C

    Biovision | Xestospongin C | 2621

    Xestospongin C is a marine natural product isolated from Pacific basin sponges; it antagonizes the calcium-releasing action of inositol-1,4,5-trisphosphate (IP3) at the receptor level. Xestospongin C...

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  • WZ-8040

    Biovision | WZ-8040 | B2205

    WZ-8040 is a potent EGFR inhibitor that suppresses the growth of EGFR-T790M (a mutation of the gatekeeper T790 residue) containing cell lines and inhibits EGFR phosphorylation.WZ-8040 is a potent...

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  • WY-14643

    Biovision | WY-14643 | 2041

    Cell-permeable. A selective PPARα agonist (EC50 values are 0.63, 32 and > 100 μM at PPARα, PPARγ and PPARδ respectively.WY-14643 is a selective PPARα agonist (EC50 values are 0.63, 32 and > 100 μM at...

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  • WST-3

    Biovision | WST-3 | 2814

    WST-3 is a highly sensitive tetrazolium reagent that produces a water-soluble, colored formazan dye with reducing agents such as NADH.WST-3 is a highly sensitive tetrazolium reagent that produces a...

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  • WST-1

    Biovision | WST-1 | 2198

    A water-soluble tetrazolium reagent that serves as a sensitive chromogenic indicator for NADH. It is reduced by NADH at neutral pHs in the presence of 1-methoxy PMS to produce the corresponding...

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  • WP-1130

    Biovision | WP-1130 | 2014

    Cell-permeable. WP1130 acts as a partly selective DUB (deubiquitinases) inhibitor, directly inhibiting DUB activity of USP9x, USP5, USP14, and UCH37, which are known to regulate survival protein...

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  • Wnt Antagonist, C59

    Biovision | Wnt Antagonist, C59 | 2063

    Cell-permeable. A potent Wnt signaling pathway inhibitor (IC₅₀ = <0.11 nM using Wnt-Luc reporter assay).Wnt Antagonist, C59 is a potent Wnt signaling pathway inhibitor (IC₅₀ = <0.11 nM using Wnt-Luc...

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  • WIKI-4

    Biovision | WIKI-4 | B1630

    WIKI4 is a potent inhibitor of Wnt/β-catenin signaling (EC50 ~ 75 nM); inhibits auto-ADP-ribosylation of tankyrase 2 (TNKS2) (IC50 ~15 nM).WIKI4 is a potent inhibitor of Wnt/β-catenin signaling (EC50...

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  • WHI-P131

    Biovision | WHI-P131 | 1853

    Cell-permeable. Selectively inhibits the tyrosine kinase activity of Jak3 with an IC₅₀ value of 78 µM without affecting the enzymatic activity of JAK1, JAK2, or other protein tyrosine kinases. Also...

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  • WDR5 0103

    Biovision | WDR5 0103 | B1125

    WDR5-0103 is a small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 nM). It inhibits the catalytic activity of MLL core complex in in vitro experiments with IC₅₀ of 39 µM. WDR5 is a...

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  • WAY-362450

    Biovision | WAY-362450 | B1631

    WAY-362450 is a highly potent, selective, and orally active farnesoid X receptor (FXR) agonist with an EC50 of 4 nM.WAY-362450 is a highly potent, selective, and orally active farnesoid X receptor...

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  • WAY-170523

    Biovision | WAY-170523 | 9607

    WAY-170523 is a potent and selective inhibitor of MMP-13 (IC₅₀ = 17 nM). Inhibits MMP-9, TACE and MMP-1 only at higher concentrations (IC₅₀ values of 945, >1000 and >10,000 nM, respectively)...

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  • VX-809

    Biovision | VX-809 | 2857

    VX-809 is a novel CFTR corrector that modulates the folding and trafficking of CFTR protein. VX-809 stabilizes an N-terminal domain in CFTR that contains only MSD1 (membrane-spanning domain 1) and...

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  • VX-765

    Biovision | VX-765 | 2781

    VX-765 is a prodrug of VRT-043198, a potent and selective inhibitor of interleukin-converting enzyme/caspase-1 subfamily caspases. VRT-043198 displays 100- to 10,000-fold selectivity against...

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  • VX-745

    Biovision | VX-745 | 2812

    VX-745 is a potent and selective inhibitor of p38α (IC₅₀ = 10 nM). It displays 22-fold greater selectivity versus p38β and no inhibition of p38γ. Also blocks TNFα production in LPS-stimulated HWB in...

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  • VX-661

    Biovision | VX-661 | B1268

    VX-661, is CFTR modulator that is potentially useful for treatment of cystic fibrosis. VX-661 corrects F508del-CFTR trafficking and increases F508del-CFTR protein activity in vitro.VX-661, is CFTR...

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  • VU0155041

    Biovision | VU0155041 | B1299

    VU0155041 is a potent, positive allosteric modulator/allosteric agonist at mGlu4 receptors (EC₅₀ = 798 and 693 nM at human and rat mGlu4 receptors respectively). Active in in vivo models of...

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  • VRT752271

    Biovision | VRT752271 | B1679

    VRT752271 is a reversible, ATP-competitive inhibitor of ERK1 and ERK2 kinases, with IC50 of <0.3 nM against ERK2.VRT752271 is a reversible, ATP-competitive inhibitor of ERK1 and ERK2 kinases, with...

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  • VK3-OCH3

    Biovision | VK3-OCH3 | 2694

    VK3-OCH3 is a Vitamin K3 (Menadione) analog that displays potent antitumor activity. It has been shown to induce G2/M arrest and apoptosis in neuroblastoma cells with much less cytotoxicity towards...

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  • Vicriviroc Malate

    Biovision | Vicriviroc Malate | 1599

    Second generation orally active CCR5 antagonist, which is also a potent inhibitor of HIV-1 entry into target cells, with a mean IC₅₀ =0.46 nM and IC₉₀ =1~10 nM to HIV isolates (n=52).Vicriviroc...

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  • Veratridine

    Biovision | Veratridine | 2422

    Veratridine is a steroidal alkaloid. Voltage-gated Na⁺ channel opener. May be used to increase Na⁺ concentration in cardiomyocytes and in cultured sympathetic neurons.Veratridine is a steroidal...

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