Kinesin
Kinesin inhibitors target kinesin motor proteins, which are responsible for transporting cellular cargo along microtubules and play a key role in cell division, particularly during mitosis. Kinesins are involved in the movement of chromosomes and other organelles during cell division. Inhibiting kinesins can disrupt these processes, leading to cell cycle arrest and potential cell death, making these inhibitors valuable in cancer research. At CymitQuimica, we offer a diverse range of high-quality kinesin inhibitors to support your research in cell biology, mitosis, and cancer therapy.
Found 89 products for "Kinesin".
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Mitotic kinesin-IN-1 hydrochloride
CAS:Mitotic kinesin-IN-1 hydrochloride (Example 80) is an inhibitor of mitotic kinesin, which suppresses cell proliferation by hindering mitosis. This compound is applicable in research related to cancer, cardiac hypertrophy, immune and inflammatory diseases, and fungal infections.Formula:C22H26ClF2N3OSColor and Shape:SolidMolecular weight:453.98RMS-07
CAS:RMS-07, a covalent MPS1/TTK inhibitor, has an IC50 of 13.1 nM, targeting a kinase hinge cysteine.Formula:C35H40N8O2Color and Shape:SolidMolecular weight:604.74EX05
CAS:EX05, an effective KIF18A inhibitor, exhibits an IC50 of 8.2 nM and holds potential for cancer research applications.Formula:C26H30F2N4O5SColor and Shape:SolidMolecular weight:548.60MKLP2-IN-1
CAS:MKLP2-IN-1 (compound 12a) is an inhibitor of MKLP2 that demonstrates excellent oral bioactivity. In vitro, MKLP2-IN-1 inhibits the ATPase activity stimulated by recombinant MKLP2 microtubules and, in a mouse Calu-6 lung cancer model, it effectively suppresses tumor growth.Formula:C23H19BrFN3O2Color and Shape:SolidMolecular weight:468.318KIF18A-IN-18
CAS:KIF18A-IN-18 (Compound I) serves as an inhibitor of KIF18A and is applicable in studies of tumors characterized by chromosomal instability.Formula:C29H34F2N4O5SMolecular weight:588.67CCT368772
CAS:CCT368772 (compound 35) is a selective inhibitor of the kinesin protein HSET, with an HSET ADP-GloIC50 of 0.019 μM. It demonstrates specificity for HSET over Eg5, as shown by an Eg5 ADP-GloIC50 value greater than 200 μM. CCT368772 (compound 152) can be utilized in the study of hyperproliferative diseases and disorders such as cancer.Formula:C25H32N6O5SMolecular weight:528.63AM-9022
CAS:AM-9022 is a potent and selective KIF18A inhibitor, orally active and suitable for cancer research [1].Formula:C27H36F2N6O4SColor and Shape:SolidMolecular weight:578.67TTK inhibitor 4
CAS:TTK inhibitor 4 (compound 16) acts as a potent threonine tyrosine kinase (TTK) inhibitor, exhibiting an IC 50 value of 0.016 μM and demonstrating anti-tumor activity [1].Formula:C25H29N9OColor and Shape:SolidMolecular weight:471.56Cenpemlin
CAS:Cenpemlin is a CENP-M inhibitor that disrupts the interaction between CENP-M and CENP-L. It is useful for studying centromere-kinetochore interactions and the dynamic assembly of kinetochores during cell division.Formula:C17H29N7O7Molecular weight:443.46
