Cytoskeleton

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Catalog No.
Product Name
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Product Citation
  1. Cnk1 inhibitor

    PHT-7.3 is a selective inhibitor of connector enhancer of kinase suppressor of Ras 1 (Cnk1) pleckstrin homology (PH) domain, which inhibits mut-KRas, but not wild-type KRas cancer cell and tumor growth and signaling.
  2. KRAS G12C covalent inhibitor

    AMG-510 is a potent, orally bioavailable, and selective KRAS G12C covalent inhibitor with anti-tumor activity.
  3. KRas G12C inhibitor

    KRAS G12C inhibitor 5 is a KRas G12C inhibitor extracted from patent WO2017201161A1, Compound example 147.
  4. KRAS G12C covalent inhibitor

    AMG-510 is a potent, orally bioavailable, and selective KRAS G12C covalent inhibitor with anti-tumor activity.
  5. KRAS G12C inhibitor

    KRAS G12C inhibitor 13 is a KRAS G12C inhibitor extracted from patent WO2018143315A1, compound 30.
  6. Epac inhibitor

    EPAC 5376753 is an allosterically inhibitor of Epac which inhibits Epac1 with an IC50 of 4 ?M in Swiss 3T3 cells.
  7. Epac1 antagonist

    CE3F4 is a selective antagonist of exchange protein directly activated by cAMP (Epac1), with IC50s of 10.7 μM and 66 μM for Epac1 and Epac2(B), respectively.
  8. Wnt/beta-catenin modulator

    KY1220 is a compound that destabilizes both β-catenin and Ras, via targeting the Wnt/β-catenin pathway; with an IC50 of 2.1 μM in HEK293 reporter cells.
  9. GGTase I inhibitor

    GGTI298 is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor, strongly inhibiting the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras, with IC50 values of 3 and > 20 μM in vivo, respectively.
  10. K-Ras inhibitor

    K-Ras-IN-1 is a K-Ras inhibitor, by binding to K-Ras in a hydrophobic pocket that is occupied by Tyr-71 in the apo-Ras crystal structure.(the detailed information refer to the reference).
  11. K-ras G12C inhibitor

    K-Ras G12C-IN-3 is a novel and irreversible inhibitor of mutant K-ras G12C.
  12. covalent K-Ras G12C inhibitor

    K-Ras G12C-IN-2 is an irreversible covalent K-Ras G12C inhibitor.
  13. K-ras G12C inhibitor

    K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C extracted from patent WO 2014152588 A1.
  14. exchange protein inhibitor

    (R)-CE3F4 is a potent and selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1), with an IC50 of 4.2 μM, with 10-fold selectivity for Epac1 over Epac2 (IC50, 44 μM).
  15. K-Ras(G12C) inhibitor

    6H05 TFA is a selective, and allosteric inhibitor of oncogenic mutant K-Ras(G12C).
  16. RhoA subfamily Rho GTPases inhibitor

    Rhosin is a potent, specific RhoA subfamily Rho GTPases inhibitor, which specifically binds to RhoA to inhibit RhoA-GEF interaction with a Kd of ~ 0.4 uM, and does not interact with Cdc42 or Rac1, nor the GEF, LARG. Rhosin induces cell apoptosis.
  17. pan GTPase inhibitor

    CID-1067700 (ML282) is a pan GTPase inhibitor, and competitively inhibits Ras-related in brain 7 (Rab7) with a Ki of 13 nM.
  18. LARG inhibitor

    Y16 is a specific inhibitor of Leukemia-associated Rho guanine nucleotide exchange factor (LARG) with a Kd value of 76 nM.
  19. RhoA subfamily Rho GTPases inhibitor

    Rhosin hydrochloride is a potent, specific RhoA subfamily Rho GTPases inhibitor.
  20. Ras inhibitor

    (rac)-Antineoplaston A10 is the racemate of Antineoplaston A10. Antineoplaston A10 is a Ras inhibitor potentially for the treatment of glioma, lymphoma, astrocytoma and breast cancer.
  21. inhibitor of Ral binding to RALBP1

    RBC10 is an inhibitor of Ral binding to RALBP1 (the effector).
  22. Rho family GTPases inhibitor

    MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases, with EC50 values ranging from 16 μM to 120 μM.
  23. MRTF pathway inhibitor

    CCG-222740 is an orally active and selective Rho/myocardin-related transcription factor (MRTF) pathway inhibitor. CCG-222740 is also a potent inhibitor of alpha-smooth muscle actin protein expression.
  24. protein-protein interactions inhibitor

    NSC-92828, also known as 3-Phenanthrenebutyric acid, is a Protein-protein interaction inhibitor (PP inhibitor or PPI).

  25. S-IIP inhibitor/KRASG12C Probe

    ARS-1323-Alkyne is a novel KRASG12C occupancy probe.

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