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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.

  • Cilazapril monohydrate

    Biovision | Cilazapril monohydrate | B2139

    Cilazapril is a pyridazine angiotensin-converting enzyme inhibitor (ACE inhibitor) used for the treatment of hypertension and congestive heart failure. It is a prodrug that is hydrolyzed after absorption to its main metabolite cilazaprilat.Cilazapril is...

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  • CID-755673

    Biovision | CID-755673 | 2660

    CID-755673 is a selective small molecule inhibitor of protein kinase D (PKD) (IC₅₀s = 182, 280, 227 nM for PKD1, 2, and 3, respectively). It exhibits higher selectivity for PKD over Akt, polo-like kinase 1, CDK activating kinase, CAMKII and three...

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  • CID-5951923

    Biovision | CID-5951923 | 2690

    CID-5951923 is an Inhibitor of Krüppel-like factor 5 (KLF5) transcription factor (IC₅₀ = 2.3 μM). Significantly reduces endogenous KLF5 protein levels and decreases viability of colon cancer cells, without affecting the nontransformed intestinal...

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  • CID-5721353

    Biovision | CID-5721353 | B1275

    CID-5721353 is a B-Cell Lymphoma 6 Inhibitor (BCL6 inhibitor). disrupted BCL6/corepressor complexes in vitro and in vivo, and was shown to bind the critical site within the BTB groove. This compound could induce expression of BCL6 target genes and kill...

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  • CID-2011756

    Biovision | CID-2011756 | 2607

    Cell-permeable. CID-2011756 is an ATP-competitive protein kinase D (PKD) inhibitor with IC₅₀ values of 0.6, 0.7 and 3.2 μM for PKD2, PKD3 and PKD1 respectively. Inhibits phorbol ester-induced endogenous PKD1 activation in LNCaP prostate cancer cells...

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  • CID 2745687

    Biovision | CID 2745687 | 1969

    Cell-permeable. A potent, competitive, and reversible antagonist of the orphan receptor GPR35 (Ki = 12.8 nM). Prevents the GPR35-mediated increase in ERK1/2 phosphorylation and β-arrestin recruitment induced by pamoic acid.CID 2745687 is a potent,...

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  • Ciclopirox Olamine

    Biovision | Ciclopirox Olamine | B2336

    Ciclopirox olamine (CPX) is an antifungal agent that has recently demonstrated promising anti-neoplastic activity against hematologic and solid tumors. Also inhibits ferroptosis.Ciclopirox olamine (CPX) is an antifungal agent that has recently...

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  • CI-994

    Biovision | CI-994 | 1742

    Cell-permeable. A histone deacetylase (HDAC) inhibitor (Ki values are 0.41, 0.75, >100 and >100 µM for HDAC1, HDAC3, HDAC6 and HDAC8 respectively). Displays significant antitumor activity in vitro and in vivo against a broad spectrum of murine and human...

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  • CHR2797

    Biovision | CHR2797 | 2720

    CHR2797 is a novel metalloenzyme inhibitor. It inhibits proliferation, and induces growth arrest and apoptosis in myeloma cells, including cells resistant to conventional chemotherapeutics.CHR2797 is a novel metalloenzyme inhibitor. It inhibits...

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  • Cholesteryl hemisuccinate

    Biovision | Cholesteryl hemisuccinate | B1978

    Cholesteryl hemisuccinate is a useful cholesterol-based detergent that increases the stability of G protein-coupled receptors (GPCRs). Together with mutagenesis studies and recent GPCR structures, it has been determined that stabilization is attained...

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  • Chlorpromazine hydrochloride

    Biovision | Chlorpromazine hydrochloride | B1992

    Chlorpromazine is a dopamine receptor antagonist; reduces neurotransmitter binding. Inhibits nitric oxide synthesis in mouse brain cytosol. Also acts as an antagonist of nAChR, histamine and 5-HT receptors. Displays growth-inhibitory effects on a variety...

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  • CHIR 99021 trihydrochloride

    Biovision | CHIR 99021 trihydrochloride | B1199

    CHIR99021 trihydrochloride is the hydrochloride salt of the potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitor CHIR99021 (Cat. No. 1677).CHIR99021 trihydrochloride is the hydrochloride salt of the potent and highly selective...

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  • CHIR 99021

    Biovision | CHIR 99021 | 1677

    A potent and highly selective inhibitor of glycogen synthase kinase-3β (GSK-3β) (IC₅₀ = 6.7 nM). CHIR99021 has been shown to allow for long-term expansion of murine embryonic stem cells in a chemically-defined medium in conjunction with MEK/MAPK...

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  • CHD-5

    Biovision | CHD-5 | 2693

    CHD-5 is a potent aryl hydrocarbon receptor (AhR) antagonist.CHD-5 is a potent aryl hydrocarbon receptor (AhR) antagonist.Biovision | 2693 | CHD-5 DataSheetAlternate Name/Synonyms:...

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  • CHAPS, High Purity

    Biovision | CHAPS, High Purity | 1545

    A zwitterionic non-denaturing detergent that protects the native state of proteins, able to disrupt non-specific protein interactions and has less protein aggregation than non-ionic detergents. It is electrically neutral and easily removed by dialysis...

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  • CH5424802

    Biovision | CH5424802 | 2867

    CH5424802 is a potent, selective, ATP-competitive inhibitor of anaplastic lymphoma kinase (ALK) (IC₅₀ = 1.9 nM). It displays potent antitumor activity against RET-rearranged non-small cell lung cancer (NSCLC).CH5424802 is a potent, selective,...

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  • CGP-57380

    Biovision | CGP-57380 | 9661

    CGP-57380 is a cell-permeable Inhibitor of MAP-kinase interacting kinase-1 (Mnk1, MKNK1) (IC₅₀ = 2.2 μM). Displays selectivity over p38, JNK1, ERK1, ERK2, PKC and c-src family kinases.CGP-57380 is a cell-permeable Inhibitor of MAP-kinase interacting...

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  • CGM097

    Biovision | CGM097 | B1820

    CGM097 is a potent and selective MDM2 inhibitor; an orally bioavailable HDM2 (human homolog of double minute 2) antagonist with potential antineoplastic activity.CGM097 is a potent and selective MDM2 inhibitor; an orally bioavailable HDM2 (human homolog...

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  • CFTR Inhibitor-172

    Biovision | CFTR Inhibitor-172 | 2487

    A potent, reversible, selective, CFTR chloride channel blocker. Inhibits CFTR short-circuit current in < 2 minutes in a voltage-independent manner (Ki = ~ 300 nM). At concentrations fully inhibiting CFTR, CFTR(inh)-172 does not block increase of cellular...

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  • CFTR Inhibitor, GlyH-101

    Biovision | CFTR Inhibitor, GlyH-101 | 2863

    CFTR Inhibitor II, or GlyH-101, is a glycine hydrazide that selectively and reversibly blocks the CFTR channel (Ki = 4.3 µM). GlyH-101 binds to a site at the external pore of CFTR, occluding the pore and rapidly preventing chloride transport.CFTR...

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  • CFI-400945

    Biovision | CFI-400945 | B1287

    CFI-400945 is a potent, ATP-competitive inhibitor of PLK4 (Polo-like kinase 4) (Ki = 0.2 nM). Displays anticancer properties. PLK4 inhibition also prevents cell division and inhibits proliferation of PLK4-overexpressing tumor cells.CFI-400945 is a...

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  • Cercosporin

    Biovision | Cercosporin | 9684

    Cercosporin is a light-induced polyketide phytotoxin reported to produce singlet oxygen when photoactivated. Acts as a potent and specific PKC inhibitor. Competes for the phorbol binding site. Anticancer compound. Also displays antiproliferative,...

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  • Ceralifimod

    Biovision | Ceralifimod | B1289

    Ceralifimod (also known as ONO-4641), is a next-generation sphingosine 1-phosphate (S1P) receptor agonist selective for S1P receptors 1 and 5. In vitro, ONO-4641 displays highly potent agonistic activities versus S1P receptors 1 and 5 (EC₅₀ values of...

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  • Cephalexin Hydrate

    Biovision | Cephalexin Hydrate | B1522

    Cephalexin is a cephalosporin antibiotic used to study the effect of expression, binding, and inhibition of PBP3 and other penicillin-binding proteins (PBPs) on bacterial cell wall mucopeptide synthesis. It is active against most Gram-positive cocci,...

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  • CEP-32496

    Biovision | CEP-32496 | 9615

    CEP-32496 specific and selective inhibitor of the activity of the mutated form (V600E) of B-raf kinase. It inhibits the activation of the RAF/mitogen-activated protein kinase kinase (MEK)/extracellular signal-related kinase (ERK) signaling pathway and...

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  • CEP-18770

    Biovision | CEP-18770 | 2433

    CEP-18770 is a reversible P2 threonine boronic acid inhibitor of the chymotrypsin-like activity of the proteasome. Displays anti-multimyeloma (MM) effect.CEP-18770 is a reversible P2 threonine boronic acid inhibitor of the chymotrypsin-like activity of...

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  • CENTA β-lactamase substrate

    Biovision | CENTA β-lactamase substrate | 2394

    CENTA is a chromogenic β-lactamase substrate that is readily hydrolyzed by β-lactamases of all classes except for the Aeromonas hydrophila metalloenzyme. Useful for kinetic studies involving β-lactamases.CENTA is a chromogenic β-lactamase substrate that...

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  • Celecoxib

    Biovision | Celecoxib | 1574

    Celecoxib is a highly selective COX-2 inhibitor and primarily inhibits prostaglandin production. Celecoxib is approximately 7.6-fold more selective for COX-2 inhibition over COX-1. This specificity allows celecoxib to reduce inflammation and pain while...

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  • Celastrol

    Biovision | Celastrol | 1940

    Cell-permeable. An Antioxidant, anti-inflammatory and immunosuppressive agent. Suppresses LPS-induced cytokine release in macrophages and monocytes (IC₅₀ = 40 nM for IL-1β and IL-1α, 80 nM for IL-6, 110 nM for prostaglandin E2 and 210 nM for IL-8 and...

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  • Cefsulodin Sodium Salt, Hydrate

    Biovision | Cefsulodin Sodium Salt, Hydrate | B1512

    Cefsulodin is a third generation cephalasporin antibiotic that inhibits cell wall synthesis. It has high activity against Pseudomonas aeruginosa with no significant activity against other gram negative bacteria. Limited activity against gram positive and...

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  • Cefoxitin Sodium Salt

    Biovision | Cefoxitin Sodium Salt | B1892

    Cefoxitin is a second-generation cephalosporin antibiotic that has been used to treat a wide range of gram-negative and gram-positive bacteria including anaerobes. It acts by interfering with bacterial cell wall synthesis and has also been shown to...

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  • Cefotaxime Sodium, USP

    Biovision | Cefotaxime Sodium, USP | B1510

    Cefotaxime sodium is a broad spectrum third generation cephalosporin antibiotic. Cefotaxime inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis...

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  • Cefazolin Sodium Salt

    Biovision | Cefazolin Sodium Salt | B1530

    Cefazolin is a broad-spectrum, first-generation cephalosporin antibiotic that is active in vitro against most Gram-positive and Gram-negative bacteria. It inhibits bacterial cell wall synthesis, causing growth to cease without lysis.Cefazolin is a...

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  • Cedrulatinib

    Biovision | Cedrulatinib | 2803

    Cerdulatinib is a novel, dual spleen tyrosine kinase (Syk) and janus kinase (JAK) inhibitor. It preferentially inhibits JAK1 and JAK3 dependent cytokine mediated signaling and functional responses in various cell types. IL2 mediated STAT5 Y694 is...

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  • Cediranib (AZD2171)

    Biovision | Cediranib (AZD2171) | 1613

    Cediranib (AZD2171) is a tyrosine kinase inhibitor that targets vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, c-KIT, and platelet-derived growth factor receptors. Studies show cediranib to be generally well tolerated as monotherapy at...

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  • C-DIM 12

    Biovision | C-DIM 12 | B2146

    C-DIM 12 activates the orphan nuclear receptor Nurr1 and inhibits bladder cancer growth. Nurr1 is a suppressor of NF-kB-related neuroinflammatory genes in microglia and astrocytes and C-DIM 12 suppresses inflammatory signaling in these cells. Displays...

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  • CCT-245737

    Biovision | CCT-245737 | B2116

    CCT-245737 is a potent and selective checkpoint kinase 1 (Chk1) inhibitor, with an IC₅₀of 1.3 nM; displays weaker activity against Chk2 (IC₅₀of 2440 nM).CCT-245737 is a potent and selective checkpoint kinase 1 (Chk1) inhibitor, with an IC₅₀of 1.3 nM;...

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  • CCT-241736

    Biovision | CCT-241736 | B2370

    CCT-241736 is a potent dual FLT3-Aurora inhibitor (IC₅₀ values against FLT3, Aurora A and Aurora B of 0.035, 0.015 and 0.1 μM respectively). CCT241736 inhibits a wide range of FLT3 mutants, including FLT3-ITD, -D835Y, -D835H, -K663Q and -N841I.CCT-241736...

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  • CCT-137690

    Biovision | CCT-137690 | B1935

    CCT137690 is a highly selective and orally bioavailable inhibitor of Aurora A, Aurora B and Aurora C with IC₅₀ of 15 nM, 25 nM and 19 nM, respectively. Displays anti-tumor activities both in vitro and in vivo. BCCT137690 is a highly selective and orally...

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  • CCT-129202

    Biovision | CCT-129202 | B1934

    CCT-129202 is a potent, ATP-competitive inhibitor of Aurora kinases with IC₅₀ values of 42 nM, 198 nM and 227 nM for Aurora A, B and C, respectively. CCT-129202 displays high selectivity for the Aurora kinases over a panel of other kinases tested and...

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  • CCF-642

    Biovision | CCF-642 | B2009

    CCF-642 is a protein disulfide isomerase (PDI) inhibitor that displays anticancer activity in multiple myeloma. Consistent with PDI inhibition, CCF642 causes acute ER stress in multiple myeloma cells accompanied by apoptosis-inducing calcium release...

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  • CC-122

    Biovision | CC-122 | B1650

    CC-122 is a novel agent for DLBCL with antitumor and immunomodulatory activity.CC-122 binds CRBN and degrades Aiolos and Ikaros resulting in a mimicry of IFN signaling and apoptosis in DLBCL.CC-122 is a novel agent for DLBCL with antitumor and...

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  • CBL0137

    Biovision | CBL0137 | B2036

    CBL0137 is a metabolically stable curaxin that activates p53 (EC₅₀ = 0.37 μM) and inhibits NF-κB (EC₅₀ = 0.47 μM). It functionally inactivates the facilitates chromatin transcription complex (FACT), driving the effects on p53 and NF-κB and promoting...

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  • CBHA

    Biovision | CBHA | 2284

    A potent histone deacetylase (HDAC) inhibitor (ID₅₀ values of 0.01 and 0.07 μM in vitro for HDAC1 and HDAC3, respectively). CBHA also induces apoptosis in nine different neuroblastoma cell lines in culture (0.5-4.0 μM) and completely suppresses...

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  • CB-839

    Biovision | CB-839 | B1179

    CB-839 is a potent, selective, and orally bioavailable inhibitor of both splice variants of glutaminase (KGA and GAC); inhibits recombinant GAC with an IC₅₀ of

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  • CB5083

    Biovision | CB5083 | B1032

    CB5083 is a potent, ATP-competitive, D2-selective, p97 inhibitor (IC₅₀ = 11 nM). In xenograft models, CB-5083 causes modulation of key p97-related pathways, induces apoptosis, and has antitumor activity in a broad range of both hematological and solid...

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  • CAY10683

    Biovision | CAY10683 | B1051

    CAY10683 is a potent histone deacetylase (HDAC) inhibitor isolated from the cyanobacterium Symploca. It inhibits HDAC2 and HDAC6 with IC₅₀ values of 0.119 and 434 nM, respectively. Inhibits HDAC4 only at higher concentrations (IC₅₀ = >1,000 nM). CAY10683...

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  • CAY-10441

    Biovision | CAY-10441 | B2353

    CAY-10441 is a potent and selective IP (prostacyclin) receptor antagonist. It displays high affinity for IP receptors. CAY-10441 antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP...

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  • CAY-10415

    Biovision | CAY-10415 | 9616

    CAY-10415 is a potent anti-diabetic drug of the TZD structural class. CAY-10415 lowers blood glucose levels in obese, hyperglycemic, hyperinsulinemic, and insulin-resistant KKAγ mice. It enhances the rate of insulin-stimulated lipogenesis in 3T3-L1...

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