Shop by Category

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.

  • Sodium Oxamate

    Biovision | Sodium Oxamate | 2580

    Oxamate is a known glycolysis inhibitor with its target being lactate dehydrogenase (LDH).Oxamate is a known glycolysis inhibitor with its target being lactate dehydrogenase (LDH).Biovision | 2580 |...

    NULL205.00 - NULL533.00
    Choose Options
  • SNX-2112

    Biovision | SNX-2112 | B2211

    SNX-2112 is a potent heat-shock protein 90 (Hsp90) inhibitor with potential antineoplastic activity. SNX-2112 selectively accumulates in tumors compared to normal tissues and binds to the N-terminal...

    NULL288.00 - NULL894.00
    Choose Options
  • SNAP-37889

    Biovision | SNAP-37889 | B2388

    SNAP-37889 is a galanin-3 receptor (GAL3) antagonist. Reduces ethanol self-administration and cue-induced re-instatement in alcohol-preferring (iP) rats with no alterations in locomotor activity or...

    NULL205.00 - NULL567.00
    Choose Options
  • Smo Antagonist, SA9

    Biovision | Smo Antagonist, SA9 | 2155

    SA9 inhibits Hh pathway by interacting directly with Smo. It inhibits SAG (Smoothened agonist) activation of Hh signaling in Shh-LIGHT 2 cells (IC₅₀ = 19 µM). Induces the localization of Smo to cilia...

    NULL214.00 - NULL378.00
    Choose Options
  • Smo Antagonist, SA1

    Biovision | Smo Antagonist, SA1 | 2154

    A Smoothened (Smo) antagonist. SA1 inhibits Hh pathway by interacting directly with Smo. Inhibits SAG (Smoothened agonist) activation of Hh signaling in Shh-LIGHT 2 cells (IC₅₀ = 3.1 µM). Also...

    NULL214.00 - NULL378.00
    Choose Options
  • Smo Agonist, SAG

    Biovision | Smo Agonist, SAG | 1939

    Cell-permeable. A Smoothened (Smo) agonist that has shown to induce Hedgehog pathway activation and counteract cyclopamine inhibition of Smo. SAG has been reported to act as an activator at low...

    NULL271.00 - NULL828.00
    Choose Options
  • SMER-3

    Biovision | SMER-3 | 2514

    SMER-3 (Small molecule enhancer of rapamycin -3) is a selective inhibitor of a yeast SCF family E3 ubiquitin ligase (SCFMet30) in vitro and in vivo. Induces the expression of MET genes that results...

    NULL337.00 - NULL861.00
    Choose Options
  • SL0101

    Biovision | SL0101 | B1895

    SL0101 is a potent and selective inhibitor of ribosomal S6 kinase (RSK) (IC₅₀ = 89 nM for RSK2). Does not have any effect on upstream kinases such as MEK, Raf and PKC. Inhibits the growth of MCF-7...

    NULL354.00 - NULL1,148.00
    Choose Options
  • SKPin C1

    Biovision | SKPin C1 | 2343

    Inhibits the cullin-RING ubiquitin E3 ligase SCF-Skp2. Selectively inhibits Skp2-mediated p27 degradation by reducing p27 binding. In cancer cells, the compound induces p27 accumulation and promotes...

    NULL222.00 - NULL639.00
    Choose Options
  • SKLB610

    Biovision | SKLB610 | 2610

    SKLB610 is a VEGFR inhibitor that potently suppresses human tumor angiogenesis. SKLB610 inhibits angiogenesis-related tyrosine kinase VEGFR2, fibroblast growth factor receptor 2 (FGFR2) and...

    NULL222.00 - NULL631.00
    Choose Options
  • SirtACt

    Biovision | SirtACt | 2741

    SirtAct is a potent Sirtuin 1 (SIRT1) activator. It increases fluorescence by 233% in a SIRT1 activity assay. SIRT1 stimulation by SirtAct leads to decreased tissue factor mediated thrombogenicity in...

    NULL239.00 - NULL697.00
    Choose Options
  • SIRT2 Inhibitor

    Biovision | SIRT2 Inhibitor | 1857

    Brain- permeable. A potent and selective sirtuin 2 deacetylase (SIRT2) inhibitor. Reduces neuronal cholesterol by inhibiting SIRT2 activity.SIRT2 inhibitor is a brain-permeable, potent and selective...

    NULL231.00 - NULL665.00
    Choose Options
  • Sildenafil citrate

    Biovision | Sildenafil citrate | 2872

    Sildenafil citrate is a potent, orally active phosphodiesterase 5 (PDE5) inhibitor (IC₅₀ = 4 nM). Inhibition of PDE5 enhances the relaxation of smooth muscle in a range of vascular tissues by...

    NULL222.00 - NULL631.00
    Choose Options
  • Shz-1

    Biovision | Shz-1 | 1915

    Cell-permeable. A sulfonylhydrazone (Shz) small molecule that acts as an enhancer of myocardial regenerative repair by stem cells. Potently induces Nkx2.5 and a subset of other cardiac markers,...

    NULL214.00 - NULL501.00
    Choose Options
  • SF-2523

    Biovision | SF-2523 | B1858

    SF-2523 is a potent and highly selective inhibitor of PI3K and BRD4 with IC₅₀ values of 16 and 241 nM for PI3Kα and BD1, respectively.SF-2523 is a potent and highly selective inhibitor of PI3K and...

    NULL222.00 - NULL631.00
    Choose Options
  • SD208

    Biovision | SD208 | 2885

    SD208 is a potent, ATP-competitive transforming growth factor-β receptor 1 (TGF-βR1) kinase inhibitor (IC₅₀ = 49 nM). Displays > 100-fold and > 17-fold selectivity over TGF-βRII and other common...

    NULL303.00 - NULL959.00
    Choose Options
  • SCR7 pyrazine

    Biovision | SCR7 pyrazine | B1119

    SCR7 pyrazine is a potent inhibitor of nonhomologous endjoining (NHEJ) mediated by DNA ligase IV. Enhances CRISPR-Cas9-mediated homology-directed repair (HDR) efficiency in vitro.SCR7 pyrazine is a...

    NULL239.00 - NULL697.00
    Choose Options
  • Sclerotiorin

    Biovision | Sclerotiorin | 2334

    An antibiotic Isolated from fungus Penicillium sp. Cholesteryl ester transfer protein (CETP) activity inhibitor (IC₅₀ = 19.4 µM). Weak antagonist of human endothelin receptor A (ETA) and B (ETB). A...

    NULL190.00 - NULL518.00
    Choose Options
  • SCH-58261

    Biovision | SCH-58261 | B1638

    SCH-58261 is the adenosine (A2A) receptor competitive antagonist. Displays 323-, 53- and 100-fold selectivity over A1, A2B and A3 receptors, respectively.SCH-58261 is the adenosine (A2A) receptor...

    NULL222.00 - NULL599.00
    Choose Options
  • SCH-529704

    Biovision | SCH-529704 | 9438

    SCH-529074 is a small molecule activator of mutant p53. It binds specifically to the p53 DBD (DNA binding domain) in a saturable manner with an affinity of 1-2 µM. Binding restores wild type function...

    NULL337.00 - NULL1,058.00
    Choose Options
  • SCD1 Inhibitor

    Biovision | SCD1 Inhibitor | 1716

    Cell-permeable. A potent and selective inhibitor of SCD1(stearoyl-CoA desaturase 1) (In vitro: IC₅₀ = 37 nM for hSCD1, <4 nM for mSCD1). Also exhibited in vivo efficacy with dose-dependent...

    NULL337.00 - NULL877.00
    Choose Options
  • SC-79

    Biovision | SC-79 | 2766

    SC-79 is an Akt activator. Binds to the pleckstrin homology (PH) domain of Akt preventing membrane translocation but paradoxically activating it in the cytosol. Enhances Akt phosphorylation by...

    NULL205.00 - NULL386.00
    Choose Options
  • SC-26196

    Biovision | SC-26196 | B1580

    SC-26196 is a selective Δ6 desaturase inhibitor (IC₅₀ = 0.2 μM in vitro. It displays selectivity over Δ5 and Δ9 desaturases (IC₅₀ values are >200 μM in vitro). Exhibits anti-inflammatory properties...

    NULL303.00 - NULL959.00
    Choose Options
  • SBHA

    Biovision | SBHA | 2202

    SBHA is a competitive histone deacetylase (HDAC) inhibitor that has been shown to inhibit HDAC1 (IC₅₀ = 0.25 μM) and HDAC3 (IC₅₀ = 0.30 μM). SBHA causes cell differentiation, cell cycle arrest, or...

    NULL182.00 - NULL418.00
    Choose Options
  • SB-742457

    Biovision | SB-742457 | 9568

    SB-742457 is a highly selective 5-HT6 receptor antagonist with potential cognition, memory and learning-enhancing effects; displays >100-fold selectivity over other receptors. in anxiolytic and...

    NULL271.00 - NULL828.00
    Choose Options
  • SB-715992

    Biovision | SB-715992 | 2468

    A potent, reversible, small molecule inhibitor of kinesin spindle protein (KSP), a kinesin motor protein essential for the formation of a bipolar mitotic spindle and cell cycle progression through...

    NULL337.00 - NULL1,058.00
    Choose Options
  • SB-525334

    Biovision | SB-525334 | 2880

    SB-525334 is a potent and selective inhibitor of transforming growth factor-β receptor I (ALK5, TGF-βRI) (IC₅₀ = 14.3 nM); displays 4-fold less potency against ALK4 (IC₅₀ = 58.5 nM) and inactive as...

    NULL303.00 - NULL959.00
    Choose Options
  • SB-415286

    Biovision | SB-415286 | B1954

    SB-415286 is a potent, selective and ATP-competitive glycogen synthase kinase-3 (GSK-3) inhibitor (Ki = 31 nM for GSK-3α). Displays minimal activity against 24 other protein kinases (IC₅₀ > 10 μ M)...

    NULL354.00 - NULL1,148.00
    Choose Options
  • SB-242235

    Biovision | SB-242235 | B2273

    SB-242235 is a potent and selective p38 MAP kinase inhibitor (IC₅₀ = 1.0 uM).SB-242235 is a potent and selective p38 MAP kinase inhibitor (IC₅₀ = 1.0 uM).Biovision | B2273 | SB-242235...

    NULL271.00 - NULL779.00
    Choose Options
  • SB239063

    Biovision | SB239063 | B1699

    SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38α MAPK while exhibited no activity against the γ- and δ-kinase isoforms.SB239063 is a potent and selective p38...

    NULL271.00 - NULL828.00
    Choose Options
  • SB 939

    Biovision | SB 939 | 2285

    An orally available pan-histone deacetylase (HDAC) inhibitor binding all HDAC isozymes with similar affinity (Kis = 16-28 nM) with the exception of HDAC6 and 7 (Kis = 247 and 104 nM, respectively)...

    NULL190.00 - NULL501.00
    Choose Options
  • Sauchinone

    Biovision | Sauchinone | 2312

    Isolated from Saururus chinensis. Displays cytoprotective and antioxidant activities in cultured hepatocytes. Suppresses NF-kB p65 activity. Neuroprotective. Bone resorption/osteoclastogenesis...

    NULL190.00 - NULL501.00
    Choose Options
  • SATA

    Biovision | SATA | 2363

    A protein modification reagent used to convert primary amine groups into protected sulfhydryls (-SH). The sulfhydryl is readily made available for use in subsequent reactions by treatment with...

    NULL239.00 - NULL1,107.00
    Choose Options
  • SAR-405

    Biovision | SAR-405 | B1286

    SAR-405 is a potent and selective PIK3C3/Vps34 inhibitor that prevents autophagy and synergizes with mTOR inhibition in tumor cells.SAR-405 is a potent and selective PIK3C3/Vps34 inhibitor that...

    NULL354.00 - NULL1,148.00
    Choose Options
  • SANT-2

    Biovision | SANT-2 | 1976

    Cell-permeable. A potent antagonist of Hedgehog (Hh) signaling pathway. Antagonizes smoothened receptor activity (KD = 12 nM) and inhibits SAG (Cat. No. 1939-500,1000) activity. SANT-2 should be a...

    NULL190.00 - NULL386.00
    Choose Options
  • SANT-1

    Biovision | SANT-1 | 1978

    Cell-permeable. A potent inhibitor of Sonic hedgehog (Shh) signaling; high affinity antagonist of smoothened activity (Kd = 1.2 nM). Inhibits smoothened agonist effects with an IC₅₀of 20 nM in...

    NULL197.00 - NULL467.00
    Choose Options
  • Salvinorin B

    Biovision | Salvinorin B | B1923

    Salvinorn B is a potent and selective κ-opioid DREADD (KORD) agonist (EC₅₀ = 11.8 nM). DREADDs are chemogenetic tools widely used to remotely control cellular signaling, neuronal activity, and...

    NULL205.00 - NULL567.00
    Choose Options
  • Salinomycin Sodium

    Biovision | Salinomycin Sodium | B1584

    Salinomycin is a polyether ionophore antibiotic that has recently been identified as an antitumor drug for several types of cancer stem cell (CSC) treatments. Salinomycin inhibits the migration and...

    NULL239.00 - NULL567.00
    Choose Options