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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.

  • Emeramide (BDTH2)

    Biovision | Emeramide (BDTH2) | 9666

    Emeramide, also known as BDTH2, is a mercury chelator and an antioxidant, for the treatment of mercury poisoning. The molecule consists of two thiol groups and linked via a pair of amide groups. BDTH2 can be used to chelate heavy metals like lead,...

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  • Eltoprazine hydrochloride

    Biovision | Eltoprazine hydrochloride | B2301

    Eltoprazine is a partial agonist at serotonin 5-HT1A, 5-HT1B, and 5-HT2B receptors (Kis = 40, 52, and 81 nM, respectively). Reduces 5-HIAA levels in the striatum and displays antiaggressive behavior in vivo.Eltoprazine is a partial agonist at serotonin...

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  • ELR-510444

    Biovision | ELR-510444 | 9433

    ELR-510444 is a potent microtube disruptor with potential anticancer activity. It displays potent microtubule-disrupting activity, causing a loss of cellular microtubules and the formation of aberrant mitotic spindles and leading to mitotic arrest and...

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  • Elesclomol (STA-4783)

    Biovision | Elesclomol (STA-4783) | B1815

    Elesclomol is a novel anticancer agent that displays oxidative stress induction, pro-apoptotic, and potential antineoplastic activities. The mechanism underlying the proapoptotic activity of elesclomol is through the induction of ROS (reactive oxygen...

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  • Elastatinal

    Biovision | Elastatinal | 9629

    Elastatinal is a potent, selective, and an irreversible elastase inhibitor (Ki = 240 nM). Elastatinal is a much stronger inhibitor of elastase from pancreas than from leucocytes. Displays antiviral activitiesElastatinal is a potent, selective, and an...

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  • EHNA hydrochloride

    Biovision | EHNA hydrochloride | 2265

    A selective inhibitor of the cGMP-specific phosphodiesterase (PDE2) (IC₅₀s = 0.8 and 2 μM from human and porcine myocardium, respectively, 3.5 μM in rat hepatocyte, and 5.5 μM in human platelet). Also a reversible adenosine deaminase inhibitor (IC₅₀ = 1...

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  • Eeyarestatin I

    Biovision | Eeyarestatin I | 9602

    Eeyarestatin I is an inhibitor of the ERAD (Endoplasmic-reticulum -associated protein degradation) pathway, blocking the degradation of misfolded proteins at a dose of 8 µM. It associates with the p97-associated deubiquitinating complex in cells,...

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  • EED-226

    Biovision | EED-226 | B1845

    EED-226 is a potent, selective, allosteric Polycomb repressive complex 2 (PRC2) inhibitor (IC₅₀ = 23.4 nM). EED-226 binds to the H3K27me3 binding pocket of EED (Embryonic Ectoderm Development) to allosterically inhibit PRC2. EED-226 induces robust and...

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  • Edoxaban Tosylate

    Biovision | Edoxaban Tosylate | 2714

    Edoxaban tosylate is an antithrombotic agent that directly inhibits Factor Xa (FXa), a key serine protease that converts prothrombin to thrombin in the coagulation cascade.Edoxaban tosylate is an antithrombotic agent that directly inhibits Factor Xa...

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  • EAI-045

    Biovision | EAI-045 | B1274

    EAI-045 is a potent and selective EGFR inhibitor. EAI-045 targets selected drug-resistant EGFR mutants but spares the wild-type receptor. EAI-045 inhibits L858R/T790M-mutant EGFR with low-nanomolar potency in biochemical assays.EAI-045 is a potent and...

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  • E-7046

    Biovision | E-7046 | B1966

    E-7046 is a specific antagonist of the type 4 prostaglandin E2 (PGE2) receptor EP4 (IC₅₀ = 13.5 nM). It possesses significant antitumor growth activity in multiple preclinical tumor models through modulating myeloid cells, including tumor-associated...

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  • E6005 (RVT-501)

    Biovision | E6005 (RVT-501) | B2263

    E6005 (RVT 501), a selective phosphodiesterase 4 (PDE4) inhibitor, developed for the treatment of atopic dermatitis.E6005 (RVT 501), a selective phosphodiesterase 4 (PDE4) inhibitor, developed for the treatment of atopic dermatitis.Biovision | B2263 |...

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  • DuP-697

    Biovision | DuP-697 | B1517

    DuP-697 is a potent and selective inhibitor of cyclooxygenase-2 (IC₅₀ values are 10 and 800 nM for COX-2 and COX-1 respectively). Inhibits prostaglandin synthesis and is anti-inflammatory in vivo.DuP-697 is a potent and selective inhibitor of...

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  • DUB Inhibitor, PR-619

    Biovision | DUB Inhibitor, PR-619 | 2302

    A cell-permeable, reversible, and broad-spectrum inhibitor of the deubiquitinylating enzymes (DUBs). Treatment of cells with PR-619 results in the accumulation of both ubiquitin and sumo-conjugated proteins.PR-619 is a cell-permeable, reversible, and...

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  • DUB Inhibitor, NSC-632839

    Biovision | DUB Inhibitor, NSC-632839 | 2570

    Cell-permeable. A pan-specific ubiquitin isopeptidase inhibitor (IC₅₀ = 45, 37 and 9.8 µM for USP2, USP7 and SENP2 respectively). NSC-632839 does not affect proteasome proteolytic activity. Induces apoptosis via a Bcl-2-dependent but...

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  • DTSSP Crosslinker

    Biovision | DTSSP Crosslinker | 2337

    KEY FEATURES & APPLICATIONS: • Water-soluble • Has primary amine-reactive N-hydroxysulfosuccinimide (Sulfo-NHS) esters at both ends • Contains cleavable, 8-atom (12 Å) spacer arm • The disulfide bond in the spacer arm is cleavable with reducing...

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  • DSDP

    Biovision | DSDP | B2416

    DSDP is a human STING agonist. It induces proinflammatory cytokine response in a human STING-dependent manner. DSDP does not have any effect on mouse STING.DSDP is a human STING agonist. It induces proinflammatory cytokine response in a human...

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  • DPPIV Inhibitor, P32/98

    Biovision | DPPIV Inhibitor, P32/98 | 2571

    Cell-permeable. A potent, specific, and competitive transition-state substrate analog inhibitor of dipeptidyl peptidase IV (DPPIV) (Ki =130 nM). May be used in cell cuture (1-10 μM) or Experimental anti-diabetic agent. Has been used in vivo and cell...

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  • DPP IV Inhibitor, NVP DPP 728

    Biovision | DPP IV Inhibitor, NVP DPP 728 | 1964

    A potent, selective, reversible, and slow binding dipeptidyl peptidase IV inhibitor (IC₅₀ = 14 nM). Displays >15,000 fold selectivity over DPP-II and a range of Proline-cleaving proteases. Displays anti-diabetic activity in vivo, improves glucose...

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  • DPP IV Inhibitor, K 579

    Biovision | DPP IV Inhibitor, K 579 | 1963

    Cell-permeable. A potent, slow binding dipeptidyl peptidase IV inhibitor with IC₅₀ values of 3, 5, 8, and 8 nM for rat, canine, human and monkey enzymes respectively. Acts as a long-acting hypoglycemic agent.DPP IV Inhibitor, K 579 is a potent, slow...

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  • DP-4978

    Biovision | DP-4978 | B1288

    DP-4978 is a potent and selective pan-RAF inhibitor with potential anticancer activity. DP-4978 displays activities against B-Raf or Ras mutant tumor cells. It binds to A-Raf, B-Raf and C-Raf isoforms with similar affinity in cells with activating...

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  • Doxycycline hyclate

    Biovision | Doxycycline hyclate | 2209

    A synthetic derivative of oxytetracycline. Acts as a broad spectrum antibiotic and matrix metallo-proteinases (MMP) inhibitor. Useful in studies involving wound healing and tissue remodeling.Doxycycline is a synthetic derivative of oxytetracycline. Acts...

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  • Dovitinib lactate

    Biovision | Dovitinib lactate | B1615

    Dovitinib (TKI258, CHIR258) is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit) with IC50 of 1 nM/2 nM, also potent to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs with IC50 of 8-13 nM, less potent to InsR, EGFR, c-Met, EphA2, Tie2,...

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  • Dorzolamide hydrochloride

    Biovision | Dorzolamide hydrochloride | B2185

    Dorzolamide Hydrochloride is an inhibitor of carbonic anhydrase, a zinc-containing enzyme that catalyzes the rapid conversion of carbon dioxide and water into carbonic acid, protons and bicarbonate ions. Distributed throughout many cells and tissues,...

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  • Dorsmorphin dihydrochloride

    Biovision | Dorsmorphin dihydrochloride | 2835

    A water-soluble derivative of the potent, reversible, AMPK inhibitor Dorsomorphin (Cat. No.1686).Dorsomorphin dihydrochloride is a potent, selective , reversible and ATP-competitive inhibitor of AMP-activated protein kinase (AMPK) (Ki = 109 nM in the...

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  • Dodecyl-β-D-maltopyranoside

    Biovision | Dodecyl-β-D-maltopyranoside | 2036

    A nonionic detergent for membrane protein stabilization and crystallization (CMC = 100 - 600 µM).Dodecyl-β-D-maltopyranoside is a nonionic detergent for membrane protein stabilization and crystallization (CMC = 100 - 600 µM).Biovision | 2036 |...

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  • D-Luciferin, Sodium Salt

    Biovision | D-Luciferin, Sodium Salt | 7902

    StayBrite™ D-Luciferin sodium salt is a useful substrate for the enzyme Firefly Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence. D-Luciferin can be utilized to assay the expression of the luciferase gene linked to a promoter...

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  • D-Luciferin, Potassium Salt

    Biovision | D-Luciferin, Potassium Salt | 7903

    D-Luciferin potassium salt is a useful substrate for the enzyme Firefly Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence. D-Luciferin can be utilized to assay the expression of the luciferase gene linked to a promoter of...

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  • D-Luciferin (Free acid)

    Biovision | D-Luciferin (Free acid) | 2779

    Synthetic. StayBrite™ D-Luciferin is a luminescent substrate for firefly luciferase (Km ~2 μM). Note: Unlike the Potassium (Cat. No.7903) or Sodium (Cat. No. 7902) salts, Luciferin free acid is not soluble in water. It requires the addition of dilute...

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  • DL-Aminoglutethimide

    Biovision | DL-Aminoglutethimide | B2040

    DL-Aminoglutethimide is a derivative of the sedative glutethimide. It acts as an aromatase inhibitor (IC₅₀ = 7.5 µM). Blocks adrenal steroidogenesis by inhibiting the enzymatic conversion of cholesterol to pregnenolone.DL-Aminoglutethimide is a...

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  • Diprotin B

    Biovision | Diprotin B | 2192

    An inhibitor of dipeptidyl aminopeptidase IV (DPP IV).Diprotin B is a dipeptidyl aminopeptidase IV (DPP IV) inhibitor.Biovision | 2192 | Diprotin B DataSheetAlternate Name/Synonyms: H-Val-Pro-Leu-OHAppearance: White solidFormulation: N/ACAS Number:...

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  • Diprotin A

    Biovision | Diprotin A | 2191

    A dipeptidyl aminopeptidase IV (DPP IV) inhibitor. Enhances recruitment of CXCR4 positive circulating endothelial progenitors to myocardium.Diprotin A is a dipeptidyl aminopeptidase IV (DPP IV) inhibitor. Enhances recruitment of CXCR4 positive...

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  • Digitonin, Water-Soluble

    Biovision | Digitonin, Water-Soluble | 2081

    Digitonin is a steroid glycoside from Digitalis purpurea. It belongs to the class of non-ionic detergents commonly used for solubilization of membrane proteins and permeabilization cellular and nuclear membranes. It permeabilizes plasma membranes of...

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  • Dibutyryl-cAMP, sodium salt

    Biovision | Dibutyryl-cAMP, sodium salt | 2769

    Dibutyryl cAMP is a cell-permeable cyclic AMP analog that activates cAMP dependent protein kinase (PKA) or the cAMP/PKA signaling pathway.Dibutyryl cAMP is a cell-permeable cyclic AMP analog that activates cAMP dependent protein kinase (PKA) or the...

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  • Diallyl trisulfide

    Biovision | Diallyl trisulfide | B1062

    Diallyl trisulfide (DATS) is an organic polysulfide compound found in garlic that acts as an H₂S donor. It displays anticancer chemotherapeutic, immunostimulatory, antioxidative, hepatoprotective, anti-fibrotic, anti-estrogenic, anti-metastatic,...

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  • Dexpramipexole dihydrochloride

    Biovision | Dexpramipexole dihydrochloride | B2215

    Dexpramipexole dihydrochloride is a neuroprotectant that may slow the progression of ALS by keeping the power on in deteriorating motor nerves. Dexpramipexole maintains mitochondrial function in people with ALS by increasing the efficiency of ATP...

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  • D-erythro-Sphingosine

    Biovision | D-erythro-Sphingosine | 2425

    D-erythro-sphingosine is an endogenous component of cell membranes found in a large family of sphingolipids. Inhibits protein kinase C (PKC).D-erythro-sphingosine is an endogenous component of cell membranes found in a large family of sphingolipids...

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  • Derazantinib (ARQ087)

    Biovision | Derazantinib (ARQ087) | B2222

    Derazantinib is an orally bioavailable inhibitor of the fibroblast growth factor receptor (FGFR) with potential antineoplastic activity. It binds to and potently inhibits the activity of FGFR subtypes 1, 2 and 3. This may result in the inhibition of...

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  • Deferoxamine Mesylate

    Biovision | Deferoxamine Mesylate | 1883

    An iron chelator used for the treatment of acute iron intoxication and of chronic iron overload due to transfusion-dependent anemias. Has been shown to have anti-proliferative effects on vascular smooth muscle cells in vitro and in vivo and to arrest...

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  • Decylubiquinone

    Biovision | Decylubiquinone | 2099

    A synthetic substrate of cytochrome and mitochondrial permeability transition pore (MPTP) inhibitor.Decylubiquinone is a synthetic substrate of cytochrome and mitochondrial permeability transition pore (MPTP) inhibitor.Biovision | 2099 | Decylubiquinone...

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  • Decernotinib (VX-509)

    Biovision | Decernotinib (VX-509) | B1260

    Decernotinib (VX-509) is a potent and selective JAK3 inhibitor (Ki = 2 nM). it has been shown to dose dependently reduce proinflammatory responses in a rat collagen-induced arthritis model and a mouse model of oxazolone-induced delayed-type...

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  • DDP-38003 dihydrochloride

    Biovision | DDP-38003 dihydrochloride | B1958

    DDP-38003 dihydrochloride is a potent, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC₅₀ of 84 nM.DDP-38003 dihydrochloride is a potent, orally available inhibitor of histone lysine-specific demethylase 1A...

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  • DBZ

    Biovision | DBZ | 2649

    DBZ is a potent γ-secretase inhibitor that blocks the cleavage of Notch into its active signaling effector, Notch intracellular domain, in human T cell lymphoma (SupT1) cells (IC₅₀ = 1.7 nM).DBZ is a potent γ-secretase inhibitor that blocks the cleavage...

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  • Daunorubicin.HCl

    Biovision | Daunorubicin.HCl | 1524

    Potent anti-cancer agent whose potential target site may be mitochondrial cytochrome c oxidase. Inhibits RNA and DNA synthesis. Also inhibits eukaryotic topoisomerase I & II. Induces DNA single strand breaks and apoptosis in HeLaS3 tumor cells...

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