MAPK

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  1. IQ-1S

    Catalog No. A16062
    JNK3 inhibitor
    IQ-1S is a Selective JNK3 inhibitor with IC50 value of 390, 360 and 87 nM for JNK1, 2 and 3 respectively. Learn More
  2. Anisomycin

    Catalog No. A11271
    SAPKs/JNKs activator
    Anisomycin is a pyrrolidine antibiotic, acts as an anti-fungal antibiotic which inhibits Protein Synthesis, also is a potent activator of SAPKs/JNKs. Learn More
  3. SR 3576

    Catalog No. A16020
    JNK3 inhibitor
    SR 3576 is a highly potent and selective JNK3 inhibitor (IC50 = 7 nM); exhibits > 2800-fold selectivity over p38. Learn More
  4. c-JUN peptide

    Catalog No. A16045
    JNK inhibitor
    c-JUN peptide is a peptide comprising residues 33 - 57 of the JNK binding (δ) domain of human c-Jun. Learn More
  5. SR 11302

    Catalog No. A14950
    AP-1 transcription factor inhibitor
    SR 11302, inhibitor of activator protein-1 (AP-1) transcription factor activity that displays antitumor effects in vivo. Learn More
  6. PNRI-299

    Catalog No. A16305
    AP-1 transcription inhibitor
    PNRI-299 is a selective AP-1 transcription inhibitor with IC50 of 20 uM without affecting NF-kappaB transcription (up to 200 μM) or thioredoxin (up to 200 μM). Learn More
  7. LGX 818 (Encorafenib)

    Catalog No. A13226
    Selective B-RAF Inhibitor
    LGX818 is an orally available Raf kinase inhibitor with potential antineoplastic activity. Learn More
  8. TAK-632

    Catalog No. A13323
    pan-RAF inhibitor
    TAK-632 is a potent pan-RAF inhibitor with favorable in vitro activity (BRAF(V600E) IC50, 2.4 nM; BRAF(wt), 8.3 nM; CRAF, 1.4 nM; pMEK (A375) IC50, 12 nM; pMEK (HMVII), 49 nM; V/B ratio. Learn More
  9. B-Raf-inhibitor 1

    Catalog No. A14122
    B-Raf inhibitor
    B-Raf inhibitor 1 is a potent and selective B-Raf inhibitor with cell IC50s of 0.31 uM and 2 nM for A375 proliferation and A375 p-ERK respectively Learn More
  10. CEP-32496 hydrochloride

    Catalog No. A15040
    Raf Inhibitor
    CEP-32496 hydrochloride is a highly potent inhibitor of wild-type BRAF, V600E mutant BRAF and c-Raf with Kd values of 14 nM, 36 nM and 39 nM, respectively. Learn More
  11. Dabrafenib Mesylate

    Catalog No. A15059
    Raf inhibitor
    Dabrafenib Mesylate is a novel, potent, and selective Raf kinase inhibitor that is capableof inhibiting the kinase activity of wild-type B-Raf, B-RafV600Eand c-Raf with IC50 values of 3.2, 0.8, and 5.0 nM, respectively. Learn More
  12. PLX7904

    Catalog No. A15855
    Raf inhibitor
    PLX7904 is a potent and selective paradox-breaker RAF inhibitor. It is able to efficiently inhibit activation of ERK1/2 in mutant BRAF melanoma cells but does not hyperactivate ERK1/2 in mutant RAS-expressing cells. Learn More
  13. ML 786 dihydrochloride

    Catalog No. A11211
    Raf inhibitor
    ML 786 dihydrochloride is a potent Raf kinase inhibitor (IC50 values are 2.1, 2.5 and 4.2 nM for B-RafV600E, C-Raf and wild-type B-Raf respectively). Learn More
  14. HG6-64-1

    Catalog No. A16022
    B-Raf inhibitor
    HG6-64-1 is a potent and selective B-Raf and mutant B-Raf inhibitor; more information can be found in Patent WO 2011090738. Learn More
  15. Regorafenib (BAY 73-4506)

    Catalog No. A10250
    VEGFR inhibitor
    Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf. Regorafenib (BAY 73-4506) is an orally bioavailable multikinase inhibitor targeting both the tumor and its vasculature. Learn More
  16. Sorafenib (Nexavar)

    Catalog No. A10001
    Raf inhibitor
    Sorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF. Learn More
  17. PLX-4720

    Catalog No. A10002
    Raf inhibitor
    PLX-4720 is a B-raf inhibitor with IC50 of 160 nM. Learn More
  18. PLX4032 (Vemurafenib)

    Catalog No. A10739
    Raf inhibitor
    PLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM. Learn More
  19. RAF265 (CHIR-265)

    Catalog No. A10773
    RAF/VEGFR Inhibitor
    RAF265 (CHIR-265) is an oral, highly selective RAF and VEGFR kinase inhibitor, which is to control or normalize VEGFR-2 along with the inhibition of B-raf and c-Raf mutation to prevent cancers. Learn More
  20. GDC-0879

    Catalog No. A10420
    B-Raf inhibitor
    GDC-0879 is a specific inhibitor of B-Raf kinase enzyme,targeting B-Raf (V600E) (IC50: 0.13 nM). Learn More
  21. AZ628

    Catalog No. A11063
    Raf inhibitor
    AZ628 is a RAF inhibitor with IC50 values: ca 30 nM for BRAF V600E and wild-type CRAF and 100 nM for wild-type BRAF. Learn More
  22. SB590885

    Catalog No. A10829
    B-Raf Inhibitor
    SB590885 is a selective small-molecule inhibitor of the B-Raf kinase and Ki app values are 0.16 and 1.72 nM for B-Raf and c-Raf respectively. Learn More
  23. ZM 336372

    Catalog No. A11077
    C-Raf inhibitor
    ZM 336372 is a potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with the paradoxical effect of inducing >100-fold activation of Raf-1 in whole cells. Learn More
  24. NVP-BHG712

    Catalog No. A10661
    EphB4 inhibitor
    NVP-BHG712 is a selective inhibitor of EphB4 kinase that exhibits selectivity for EphB4 over more than 40 other kinases in vitro, including FGFR3. Learn More
  25. Raf265 derivative

    Catalog No. A10774
    RAF/VEGFR Inhibitor
    Raf265 derivative is a derivative of Raf265 that is an oral, highly selective RAF and VEGFR kinase inhibitor with IC50 of of 5 to 10 μM. Learn More
  26. Dabrafenib (GSK2118436A)

    Catalog No. A11381
    Raf inhibitor
    Dabrafenib is a potent and selective inhibitor of B-RAF protein kinase carrying V600E mutation, currently in clinical trial. Learn More
  27. GW 5074

    Catalog No. A11436
    Raf-1 Inhibitor
    GW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor Learn More
  28. MLN2480 (BIIB-024)

    Catalog No. A11240
    pan-Raf inhibitor
    MLN 2480 is an oral, selective pan-Raf kinase inhibitor in chinical trials. Learn More
  29. PF-04880594

    Catalog No. A12739
    RAF inhibitor
    PF-04880594 is an inhibitor of RAF with IC50 values of 0.19 nM/0.13 nM and 0.39 nM for BRAF/BRAFV599E and c-RAF, respectively. Learn More
  30. Diazepinomicin

    Catalog No. A12891
    RAS/RAF/MAPK inhibitor
    Diazepinomicin, also known as TLN-4601, is a small-molecule inhibitor of the RAS/RAF/MAPK signaling pathway with potential antineoplastic activity. Learn More
  31. L-779450

    Catalog No. A13525
    Raf inhibitor
    L-779450 is a raf kinase inhibitor, a potential treatment for neurotraumatic diseases. Learn More
  32. BRAF inhibitor

    Catalog No. A11333
    BRAF inhibitor
    BRAF inhibitor is a potent BRAF inhibitor. Learn More
  33. CEP-32496

    Catalog No. A13772
    Raf inhibitor
    CEP-32496 is an orally available v-raf murine sarcoma viral oncogene homolog B1 (B-raf) serine/threonine protein kinase inhibitor with potential antineoplastic activity. Learn More
  34. Regorafenib monohydrate

    Catalog No. A15218
    Tyrosine kinase inhibitor
    Regorafenib is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDGFRβ, Kit, RET and Raf-1 with IC50 of 13 nM/4.2 nM/46 nM, 22 nM, 7 nM, 1.5 nM and 2.5 nM, respectively. Learn More
  35. Locostatin

    Catalog No. A16079
    RKIP/Raf1 inhibitor
    Locostatin is a cell permeable, potent inhibitor of Raf kinase inhibitor protein (RKIP)/Raf1 kinase interaction and an inhibitor of cell migration. Learn More
  36. PLX8394

    Catalog No. A16840
    BRAF inhibitor
    PLX8394 is a next-generation, orally available, small-molecule BRAF inhibitor with IC50 values of 3.8 nM, 14 nM and 23 nM for BRAF(V600E), WT BRAF and CRAF respectively. It has potential antineoplastic activity. Learn More
  37. LXH254

    Catalog No. A16841
    pan-RAF inhibitor
    LXH254 is a type II ATP-competitive inhibitor that inhibits both B- and CRAF kinase activities at picomolar concentrations with a high degree of selectivity against a panel of 456 human kinases and in cell-based assays. Learn More
  38. RAF709

    Catalog No. A16842
    raf kinase inhibitor
    RAF709 is a potent inhibitor of B/C RAF kinase with almost equivalent IC50 values of 0.4 nM for B-RAF and C-RAF, showing a high level of selectivity, demonstrating greater than 99% on-target binding to BRAF, BRAFV600E, and CRAF at 1 μM and very few off-targets with DDR1 (>99%), DDR2 (86%), FRK (92%), and PDGFRb (96%), the only kinases with binding >80% at 1 μM. Learn More
  39. Lifirafenib (BGB-283)

    Catalog No. A16844
    BRAF inhibitor
    Lifirafenib (BGB-283), also known as Beigene-283, potently inhibits RAF family kinases and EGFR activities in biochemical assays with IC50 values of 23, 29 and 495 nM for the recombinant BRAFV600E kinase domain, EGFR and EGFR T790M/L858R mutant. Learn More
  40. OTS964

    Catalog No. A14331
    TOPK inhibitor
    OTS964 is a potent TOPK inhibitor with an IC50 value of 28 nM. Learn More
  41. OTS514

    Catalog No. A16023
    TOPK inhibitor
    OTS514, a thieno[2,3-c]quinolone compound, is a highly potent TOPK inhibitor with an IC50 value of 2.6 nM. The compound can inhibit TOPK kinase activity. Learn More
  42. HI TOPK 032

    Catalog No. A16042
    TOPK inhibitor
    HI-TOPK-032 is a potent and selective TOPK inhibitor. In vitro, HI-TOPK-032 strongly suppressed TOPK kinase activity but had little effect on extracellular signal-regulated kinase 1 (ERK1), c-jun-NH2-kinase 1, or p38 kinase activities. Learn More
  43. CGP 57380

    Catalog No. A13883
    MNK2 inhibitor
    CGP 57380 is an inhibitor of MAP-kinase interacting kinase-1 (Mnk1, MKNK1) (IC50 = 2.2 uM). Learn More
  44. Cercosporamide

    Catalog No. A15362
    Mnk2/JAK3 inhibitor
    Cercosporamide, an usnic amide, was originally identified in Cercosporidium henningsii as a host-selective phytotoxin and broad-spectrum antifungal agent and is a potent inhibitor of MAP-kinase interacting kinase-2 (Mnk2; IC50 = 11 nM), JAK3 (IC50 = 31), and Mnk1 (IC50 = 116 nM). Learn More
  45. URMC-099

    Catalog No. A14219
    MLK inhibitor
    URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively. Learn More
  46. ML264

    Catalog No. A15866
    KLF5 inhibitor
    ML264 is a selectively inhibitor of kruppel-like factor 5 (KLF5) that potently Inhibits Growth of Colorectal Cancer. Learn More

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