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Biovision

  • CEP-33779

    Biovision | CEP-33779 | B2473

    CEP-33779 is a potent and orally available inhibitor of JAK2 (IC₅₀ = 1.3 nM). It displays 65-fold selectivity for JAK2 over JAK3. CEP-33779 induces regression of established colorectal tumors,...

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  • Alvimopan

    Biovision | Alvimopan | B2472

    Alvimopan is a peripherally acting μ-opioid receptor antagonist (Ki = 0.47 nM) that is selective over the κ- and δ-opioid receptors (Ki's = 100 nM and 12 nM, respectively). It is used to avoid...

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  • dBET6

    Biovision | dBET6 | B2471

    dBET6 is a highly potent, selective and cell-permeable degrader of BET based on PROTAC, with an IC₅₀ of 14 nM. dBET6 prompts a collapse of global elongation that phenocopies CDK9 inhibition. Displays...

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  • PF-04965842

    Biovision | PF-04965842 | B2470

    PF-04965842 (Abrocitinib) is a potent, selective, orally bioavailable JAK1 inhibitor (IC₅₀ = 29 nM). It displays excellent selectivity for JAK1 versus other JAK family enzymes.PF-04965842...

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  • Reparixin

    Biovision | Reparixin | B2469

    Reparixin is a non-competitive allosteric inhibitor of the chemokine receptors CXCR1 and CXCR2 activation with IC₅₀s of 1 and 100 nM, respectively. Blocks a range of activities including leukocyte...

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  • PF-3084014

    Biovision | PF-3084014 | B2468

    PF-3084014 (Nirogacestat) is a potent and selective gamma-secretase inhibitor (IC₅₀ of 6.2 nM). Reduces Aβ in brain, CSF and plasma in mice and guinea pigs.PF-3084014 (Nirogacestat) is a potent and...

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  • PF-04449913

    Biovision | PF-04449913 | B2467

    PF-04449913 is a potent and orally bioavailable smoothened (SMO) inhibitor. PF-04449913 binds to human SMO with an IC₅₀ of 4 nM. It has been shown to attenuate leukemia stem cell self-renewal and...

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  • Sulfatinib

    Biovision | Sulfatinib | B2466

    Sulfatinib is a potent, orally bioavailable and highly selective tyrosine kinase inhibitor against VEGFR1/2/3, FGFR1 and CSF1R with IC₅₀s of in a range of 1 to 24 nM.Sulfatinib is a potent, orally...

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  • Amrinone

    Biovision | Amrinone | B2465

    Amrinone is a potent phosphodiesterase 3 (PDE3) inhibitor (IC₅₀ = 19.5 µM). It increases developed tension and contractile force in isolated cat papillary muscle. It also displays positive inotropic...

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  • Lanreotide acetate

    Biovision | Lanreotide acetate | B2464

    Lanreotide is a synthetic polypeptide analogue of somatostatin that resembles the native hormone in its ability to suppress levels and activity of growth hormone, insulin, glucagon and many other...

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  • Indisulam

    Biovision | Indisulam | B2463

    Indisulam is a novel sulfonamide antitumor agent that displays potent antitumor activity in vitro and in vivo. It affects cell cycle progression in human tumor cells. Indisulam also acts as a...

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  • ARRY-797

    Biovision | ARRY-797 | B2462

    ARRY-797 is a potent and selective p38 mitogen-activated protein kinase inhibitor. Inhibits LPS-Induced IL-6 and In Vivo Growth of RPMI-8226 Human Multiple Myeloma Cells.ARRY-797 is a potent and...

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  • BIBF-0775

    Biovision | BIBF-0775 | B2461

    BIBF-0775 is a potent and selective transforming growth factor β (TGFβ) type I receptor (Alk5) inhibitor (IC₅₀ = 34 nM).BIBF-0775 is a potent and selective transforming growth factor β (TGFβ) type I...

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  • PZ-2891

    Biovision | PZ-2891 | B2460

    PZ-2891 (PZ2891) a specific, allosteric, brain-permeable, pantothenate kinase (PANK) modulator. it acts as both an orthosteric inhibitor (IC₅₀ =1.3 nM, hPANK3) and an allosteric activator of PANK3...

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  • HDM-201

    Biovision | HDM-201 | B2459

    Siremadlin (NVP-HDM201) is a potent and highly specific MDM-2/p53 inhibitor. It binds to human MDM2 protein with a picomolar Ki value (0.21 nM). It activates p53 and induces robust p53-dependent cell...

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  • Erdafitinib

    Biovision | Erdafitinib | B2458

    Erdafitinib is a potent and selective orally bioavailable, pan fibroblast growth factor receptor (FGFR) inhibitor with potential antineoplastic activity. It inhibits FGFR1/2/3/4 with IC₅₀s of 1.2, 2...

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  • Garenoxacin

    Biovision | Garenoxacin | B2457

    Garenoxacin is a potent des-F(6)-quinolone antibacterial agent and a topoisomerase II inhibitor.Garenoxacin is a potent des-F(6)-quinolone antibacterial agent and a topoisomerase II inhibitor...

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  • Vitamin A

    Biovision | Vitamin A | B2456

    Vitamin A is an intermediate in retinol metabolism in animals. It is metabolized to retinoic acid, a ligand for both the retinoic acid receptor (RAR) and the retinoid X receptor (RXR). roles in...

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  • Phytol

    Biovision | Phytol | B2455

    Phytol is a diterpene alcohol commonly used as an aromatic ingredient in many fragrance compounds. Phytol and its metabolites have been reported to activate retinoid X receptors (RXRs) and to promote...

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  • LXR-623

    Biovision | LXR-623 | B2454

    LXR-623 is a potent and selective LXR (liver X receptor) agonist. Reduces total serum cholesterol and LDL cholesterol, and inhibits lesion growth in models of atherosclerosis. Increases ABCA1 and...

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  • BTK Inhibitor II

    Biovision | BTK Inhibitor II | B2453

    BTK inhibitor II is a potent Bruton's tyrosine kinase (BTK) inhibitor.BTK inhibitor II is a potent Bruton's tyrosine kinase (BTK) inhibitor.Biovision | B2453 | BTK Inhibitor II DataSheetAlternate...

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  • GSK-626616

    Biovision | GSK-626616 | B2452

    GSK-626616 is a potent and selective DYRK inhibitor (IC₅₀ = 0.7 nM); inhibits other members of the DYRK family, e.g., DYRK1A and DYRK2, with similar potency. Displays ~20-fold selectivity over casein...

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  • KL001

    Biovision | KL001 | B2449

    KL001 is a cryptochrome protein (CRY) stabilizer. It blocks ubiquitin-dependent degradation of CRY, resulting in lengthening of the circadian period. Represses glucagon-induced hepatic...

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  • Carmofur

    Biovision | Carmofur | B2448

    Carmofur is derivative of 5-flurouracil (Cat. No. B1519) that acts as an inhibitor of acid ceramidase (IC₅₀ = 79 nM for the rat enzyme). It reduces acid ceramidase activity in a dose- and...

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  • Carglumic acid

    Biovision | Carglumic acid | B2447

    Carglumic acid is an activator of carbamoyl phosphate synthetase 1 (CPS1), the first enzyme in the urea cycle that is responsible for removal and detoxification of ammonia, making this drug a...

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  • Anagrelide

    Biovision | Anagrelide | B2446

    Anagrelide is a phosphodiesterase 3 (PDE3) inhibitor (IC₅₀ = 36 nM) with antiplatelet activity. Anagrelide inhibits the maturation of megakaryocytes into platelets, reducing both megakaryocyte...

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  • Amsacrine

    Biovision | Amsacrine | B2445

    Amsacrine is a potent DNA intercalating and an antineoplastic agent. One of the ways amsacrine works is by blocking an enzyme topoisomerase 2. It is effective in the treatment of acute leukemias and...

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  • Altretamine

    Biovision | Altretamine | B2444

    Altretamine is an alkylating agent with antineoplastic and antiproliferative activity. It also acts as a chemosterilant for male houseflies and other insects.Altretamine is an alkylating agent with...

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  • Atuveciclib

    Biovision | Atuveciclib | B2440

    Atuveciclib (BAY-1143572) is a potent and selective CDK9/P-TEFb inhibitor (IC₅₀ = 6 nM for CDK9/CyclinT1); displays >150-fold selectivity over CDK1/2/3/5/6/7 (IC₅₀ >800 nM). Exhibits anticancer...

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  • Tenalisib

    Biovision | Tenalisib | B2439

    Tenalisib is a potent, and selective PI3Kδ and PI3Kγ inhibitor with IC₅₀ values of 25 and 33 nM, respectively. Displays good selectivity over p110α (>300-fold) and p110β (>100-fold) isoforms...

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  • INCB057643

    Biovision | INCB057643 | B2438

    INCB057643 is a potent and selective BET inhibitor; displays more effectivity against androgen-dependent (VCaP and LNCaP) than androgen-independent (DU145 and PC3) cells with IC50 of 500 nM,...

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  • Adavivint

    Biovision | Adavivint | B2437

    Adavivint is a potent and selective Wnt pathway inhibitor with an EC₅₀ of 3 nM in vitro; induces hMSC differentiation into mature, functional chondrocytes and decreases cartilage catabolic marker...

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  • IDF-11774

    Biovision | IDF-11774 | B2436

    IDF-11774 is a potent hypoxia-inducible factor (HIF)-1 inhibitor (IC₅₀ = 3.65 μM)IDF-11774 is a potent hypoxia-inducible factor (HIF)-1 inhibitor (IC₅₀ = 3.65 μM)Biovision | B2436 | IDF-11774...

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  • Leniolisib

    Biovision | Leniolisib | B2435

    Leniolisib is a potent and selective PI3Kδ inhibitor with an IC₀ of 11 nM; displays >20-fold, 40-fold, and 200-fold selectivity over PI3Kα, PI3Kβ, and PI3Kγ, respectively; shows 30-fold cellular...

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  • EX-229

    Biovision | EX-229 | B2434

    EX-229 is a potent and allosteric activator of AMP-activated protein kinase (AMPK). In rat epitrochlearis muscle, ex229 dose-dependently increases AMPK activity of α1-, α2-, β1- and β2-containing...

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  • EBI-2511

    Biovision | EBI-2511 | B2433

    EBI-2511 is a highly potent and orally active EZH2 inhibitor with an IC₅₀ of 4 nM for EZH2(A667G). EBI-2511 displays excellent in vivo efficacy in Pfeiffer tumor Xenograft models in mouse and could...

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  • LIT-927

    Biovision | LIT-927 | B2432

    LIT-927 is a locally and orally active CXCL12 neutraligand (Ki = 267 nM for CXCL12-TR binding). Displays anti-inflammatory effect in a murine model of allergic airway hypereosinophilia.LIT-927 is a...

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  • MK-3903

    Biovision | MK-3903 | B2431

    MK-3903 is a potent and selective AMP-activated protein kinase (AMPK) activator (EC₅₀ = 8 nM).MK-3903 is a potent and selective AMP-activated protein kinase (AMPK) activator (EC₅₀ = 8 nM).Biovision |...

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  • HS-1371

    Biovision | HS-1371 | B2430

    HS-1371 is a potent RIP3 kinase inhibitor (IC₅₀ = 20.8 nM). It binds to the ATP binding pocket of RIP3 and inhibits ATP binding to prevent RIP3 enzymatic activity in vitro. . It inhibits TNF-induced...

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  • TH-34

    Biovision | TH-34 | B2429

    TH-34 is a HDAC inhibitor that displays selectivity for HDACs 6, 8 and 10 over HDACs 1, 2 and 3. TH34 induces DNA damage-mediated cell death in human high-grade neuroblastoma cell lines.TH-34 is a...

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  • GSK-2814338

    Biovision | GSK-2814338 | B2426

    GSK-2814338 is a potent Lp-PLA2 inhibitor useful for the treatment of atherosclerosis and Alzheimer's diseaseGSK-2814338 is a potent Lp-PLA2 inhibitor useful for the treatment of atherosclerosis and...

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  • BIIE 0246

    Biovision | BIIE 0246 | B2424

    BIIE 0246 is a potent, selective and competitive non-peptide antagonist for the neuropeptide Y Y2 receptor (IC₅₀ = 15 nM). BIIE 0246 displays > 650-fold selectivity over Y1, Y4 and Y5 receptors.BIIE...

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  • BMS-986142

    Biovision | BMS-986142 | B2420

    BMS-986142 is a potent, selective, and reversible BTK (Bruton’s tyrosine kinase) inhibitor (BTK IC₅₀ = 0.5nM; human WB IC₅₀ = 90 nM). BMS-986142 displays robust efficacy in murine models of...

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