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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.

  • MSX-130

    Biovision | MSX-130 | B2157

    MSX-130 is CXCR4 AntagonistMSX-130 is CXCR4 AntagonistBiovision | B2157 | MSX-130 DataSheetAlternate Name/Synonyms: 2,2'-(1,4-Phenylene)bis[4,5-diphenyl-1H-imidazole]Appearance: Cystalline...

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  • MSC-2530818

    Biovision | MSC-2530818 | B1975

    MSC-2530818 is a potent, selective CDK8 Inhibitor (IC₅₀ = 2.6 nM). It displays potent inhibition of phospho-STAT1SER727, an established biomarker of CDK8 activity. MSC2530818 demonstrates potent...

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  • MRL-24

    Biovision | MRL-24 | 2764

    Cell-permeable. MRL-24 displays high affinity for PPARγ with excellent anti-diabetic activity in mice but poor PPARγ agonist activity in transcription and adipogenesis assays. Highly effective (30...

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  • MPEP hydrochloride

    Biovision | MPEP hydrochloride | B1151

    MPEP hydrochloride is a highly selective and potent non-competitive antagonist at the mGlu5 (metabotropic glutamate receptor subtype 5) receptor subtype (IC₅₀ = 36 nM). It is a positive allosteric...

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  • MOZ-IN-3

    Biovision | MOZ-IN-3 | B2245

    MOZ-IN-3 is a potent inhibitor of MOZ, a member of histone acetyltransferases (IC₅₀ = 55 nM).MOZ-IN-3 is a potent inhibitor of MOZ, a member of histone acetyltransferases (IC₅₀ = 55 nM).Biovision |...

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  • MoTP

    Biovision | MoTP | 1852

    A useful tool for elucidating melanocyte stem cell regeneration, recruitment and maintenance mechanisms. Specifically ablates zebrafish larval melanocytes or melanoblasts, and this melanocytotoxicity...

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  • Monensin A Sodium

    Biovision | Monensin A Sodium | B1623

    Sodium Monensin, isolated from Streptomyces cinnamonensis, is a well-known representative of naturally polyether ionophore antibiotics. It preferentially forms complexes with monovalent cations to...

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  • MnTBAP Chloride

    Biovision | MnTBAP Chloride | 2058

    A cell-permeable superoxide dismutase (SOD) mimetic and potent inhibitor of peroxynitrite-induced oxidative reactions (peroxynitrite scavenger), but not a scavenger of nitric oxide (NO). Protects T...

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  • MN64

    Biovision | MN64 | B1127

    MN64 is a potent and selective tankyrase (TNKS) inhibitor (IC₅₀ values of 6 and 72 nM for TNKS1 and TNKS2 respectively). It has no effect on PARP-1 or PARP-2 (IC₅₀ > 19 µM). Through its effects on...

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  • MMP-13 inhibitor

    Biovision | MMP-13 inhibitor | 2392

    CL-82198 is a selective inhibitor of MMP-13 (IC₅₀ = 10 µM). It displays no activity against MMP-1, MMP-9 or TACE.CL-82198 is a selective inhibitor of MMP-13 (IC₅₀ = 10 µM). It displays no activity...

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  • MMAE

    Biovision | MMAE | B2344

    MMAE (Monomethyl auristatin E) is a synthetic derivative of dolastatin 10 that functions as a potent mitotic inhibitor by inhibiting tubulin polymerization. Suppresses tumor cell viability in vitro...

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  • MLS-573151

    Biovision | MLS-573151 | 1929

    Cell-permeable. A potent and specific inhibitor of Cdc42, a small GTPase of the Rho subfamily (IC₅₀ = 2 µM).MLS-573151 is a potent and specific inhibitor of Cdc42, a small GTPase of the Rho subfamily...

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  • MLR-1023

    Biovision | MLR-1023 | 2685

    MLR-1023 is an allosteric activator of Lyn kinase (EC₅₀ = 63 nM). It reduces blood glucose levels without increasing insulin secretion in vivo. MLR-1023 does not activate peroxisome...

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  • MLN-9708

    Biovision | MLN-9708 | B2195

    MLN-9708 is a prodrug of Ixazomib citrate (MLN-2238). MLN-9708 is an orally bioavailable next-generation proteasome inhibitor (PI) with potential potent anticancer activity in both hematologic and...

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  • MLN8237

    Biovision | MLN8237 | 2718

    MLN8237 is a potent and selective inhibitor of Aurora kinase A (IC₅₀ =1.2 nM). It displays >200-fold higher selectivity for Aurora kinase A over Aurora kinase B. Displays antineoplastic activity...

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  • MLN-8054

    Biovision | MLN-8054 | B1943

    MLN-8054 is a potent and selective inhibitor of Aurora kinase A (IC₅₀ = 4 nM). Displays 40-fold selectivity for Aurora A over Aurora B.MLN-8054 is a potent and selective inhibitor of Aurora kinase A...

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  • MLN-4924

    Biovision | MLN-4924 | 2566

    A potent and selective inhibitor of NEDD8 (Neural precursor cell expressed, developmentally down-regulated 8)-activating enzyme (NAE) (IC₅₀ = 4.7 nM) with potential anticancer activity. NAE activates...

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  • MLN2480

    Biovision | MLN2480 | B1706

    MLN 2480(BIIB-024) is an oral, selective pan-Raf kinase inhibitor in clinical trials.MLN 2480(BIIB-024) is an oral, selective pan-Raf kinase inhibitor in clinical trials.Biovision | B1706 | MLN2480...

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  • ML-7 hydrochloride

    Biovision | ML-7 hydrochloride | B2000

    ML-7 hydrochloride is a selective MLCK (myosin light chain kinase) inhibitor (Ki = 0.3 μM). Displays reversible, ATP-competitive inhibition of Ca²⁺-calmodulin-dependent and -independent smooth muscle...

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  • ML-365

    Biovision | ML-365 | B2076

    ML-365 is a potent and selective TASK-1 (K2P3.1/KCNK3) channel blocker (IC₅₀ values are 4 and 390 nM at TASK-1 and TASK-3, respectively). Displays little or no inhibition at Kir2.1, voltage-gated...

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  • ML-354

    Biovision | ML-354 | 9415

    ML-354 is a selective PAR4 antagonist (IC₅₀ = 140 nM). Displays 71-fold selectivity for PAR4 over PAR1 (PAR-1 IC₅₀ = 10 μM).ML-354 is a selective PAR4 antagonist (IC₅₀ = 140 nM). Displays 71-fold...

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  • ML-35

    Biovision | ML-35 | B2077

    ML-335 is a potent, selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2) channels activator with EC₅₀ of 14.3 and 5.2 uM, respectively.ML-335 is a potent, selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2)...

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  • ML-324

    Biovision | ML-324 | 2763

    Cell-permeable. ML-324 is a JMJD2 histone demethylase inhibitor (JMJD2 IC₅₀ = 920 nM). Represses the expression of viral (HCMV and HSV-1) immediate early genes (IC₅₀ ~ 10 µM) and abrogates infection...

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  • ML243

    Biovision | ML243 | 2515

    ML-243 is a selective inhibitor of cancer stem cells. Displays 32-fold selective inhibition of a breast cancer stem cell-like cell line (EC₅₀ = 2.0 µM) over a control (mammary epithelial) cell line...

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  • Ml241

    Biovision | Ml241 | 2697

    ML241 is a potent, selective, and reversible inhibitor of the AAA ATPase p97 (IC₅₀ = 100 nM). It blocks p97-dependent proteasome substrate with an IC₅₀ of ~ 3500 nM.ML241 is a potent, selective, and...

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  • ML-240

    Biovision | ML-240 | B1142

    ML-240 is an ATP-competitive inhibitor of the D2 domain of the p97 ATPase (IC₅₀ = 110 nM). It disrupts the endoplasmic reticulum-associated degradation and autophagy pathways, preventing the...

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  • ML230

    Biovision | ML230 | B2389

    A selective ATP-Binding Cassette Subfamily G Member 2 Efflux Inhibitor. displays selectivity toward ABCG2 over ABCB1ML230 is a selective ATP-Binding Cassette Subfamily G Member 2 Efflux Inhibitor...

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  • ML-204

    Biovision | ML-204 | 9448

    ML-204 is a selective blocker of TRPC4 channels. Displays 19-fold selectivity against TRPC6 and 9-fold selectivity against TRPC5; shows no significant activity at TRPV1, TRPV3, TRPA1 and TRPM8...

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  • ML-162

    Biovision | ML-162 | B2304

    ML-162 is a GPX4 (glutathione peroxidase 4) inhibitor that is selectively lethal to mutant RAS oncogene-expressing cell lines (IC₅₀s = 25 and 578 nM for HRASG12V-expressing and wild-type BJ...

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  • ML161

    Biovision | ML161 | 2689

    ML161 is an allosteric Inhibitor of protease-activated receptor 1 (PAR1)-mediated platelet activation (IC₅₀ = 0.26 μM for the inhibition of platelet P-selectin expression on human platelets). Also...

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  • ML130

    Biovision | ML130 | 1974

    Cell-permeable. A selective NOD1 (nucleotide-binding oligomerization domain 1) inhibitor. Selectively inhibits NOD1-dependent activation of NF-kB in HEK293 cells (IC₅₀ = 0.56±0.04 µM). Displays high...

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  • MK-8931

    Biovision | MK-8931 | B1315

    MK-8931 is a potent BACE1 inhibitor. MK-8931 binds significantly to β-secretase.MK-8931 is a potent BACE1 inhibitor. MK-8931 binds significantly to β-secretase.Biovision | B1315 | MK-8931...

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  • MK-7655

    Biovision | MK-7655 | B2289

    MK-7655 is a potent and selective β-lactamase inhibitor. It restores imipenem-susceptibility in imipenem-resistant K. pneumoniae and P. aeruginosa when used at concentrations of 12.5 and 4.7 μM,...

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  • MK-571 sodium

    Biovision | MK-571 sodium | 2692

    MK-571 sodium is the sodium salt of the multidrug resistance protein-1 (MRP1) inhibitor MK-571 (Cat. No. 2691).MK-571 sodium is a selective, CysLT1 receptor antagonist. It blocks the binding of...

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  • MK-571

    Biovision | MK-571 | 2691

    MK 571 is a selective, CysLT1 receptor antagonist. It blocks the binding of leukotriene LTD4, but not LTC4, to human and guinea pig lung membranes with Ki values of 0.22 nM and 2.1 nM, respectively...

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  • MK-5172

    Biovision | MK-5172 | B2118

    MK-5172 is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants.MK-5172 is a selective inhibitor of Hepatitis C virus NS3/4a protease...

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  • MK-4827 (Tosylate)

    Biovision | MK-4827 (Tosylate) | B2003

    MK-4827 is a potent and selective PARP-1 and PARP-2 inhibitor with IC₅₀ values of 3.8 nM and 2.1 nM, respectively. It induces synthetic lethality in preclinical tumor models with loss of BRCA and...

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  • MK-4827

    Biovision | MK-4827 | 9462

    MK-4827 is a potent and selective PARP-1 and PARP-2 inhibitor with IC₅₀ values of 3.8 nM and 2.1 nM, respectively. It induces synthetic lethality in preclinical tumour models with loss of BRCA and...

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  • MK-3102

    Biovision | MK-3102 | 9599

    MK-3102 is a potent, selective and long-acting dipeptidyl peptidase-4 (DPP-4) inhibitor with IC₅₀ of 1.6 nM; highly selective over other proteases (QPP, DPP8, and FAP) tested.MK-3102 is a potent,...

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  • MK-2206

    Biovision | MK-2206 | 1888

    A highly selective non-ATP competitive allosteric Akt inhibitor with IC₅₀’s of 8 nM, 2 nM and 65 nM for Akt1, Akt2 and Akt3, respectively. MK-2206 potently inhibits phosphorylation of Thr³⁰⁸ and...

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  • MK-1775

    Biovision | MK-1775 | 2373

    MK-1775 is a potent and selective inhibitor of the tyrosine kinase WEE1 (IC₅₀ = 5.2 nM). It selectively targets and inhibits WEE1, a tyrosine kinase that phosphorylates cyclin-dependent kinase 1...

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  • MK-1439

    Biovision | MK-1439 | B1250

    MK-1439 (also known as Doravirine), is a non-reversible reverse transcriptase inhibitor used in the treatment of HIV/AIDS with IC50 values of 12, 9.7, and 9.7 nM against the wild type (WT), K103N and...

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  • MK-0941

    Biovision | MK-0941 | B1207

    MK-0941 is selective, allosteric glucokinase activator (GKA) that activates glucokinase (hexokinase subtype IV) with greater selectivity than over different hexokinase isoforms. MK-0941 shows...

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