K-858
A potent, selective inhibitor of mitotic kinesin Eg5 ATPase activity with IC50 of 1.3 uM; displays >150-fold more selective for Eg5 than other members of the kinesin superfamily; induces mitotic arrest, apoptosis, and cell growth inhibition through the activation of the Mad2-mediated spindle checkpoint, and has no effect on microtubule polymerization; exhibits potent antitumor activity in xenograft models of cancer, and induces the accumulation of mitotic cells with monopolar spindles in tumor tissues.Breast Cancer Preclinical.
Product Specifications
CAS Number
72926-24-0
Product Name Alternative
K-858 | K 858
Purity
>98% (HPLC)
Solubility
10 mM in DMSO
Smiles
CC (NC1=NN (C (C) =O) C (C2=CC=CC=C2) (C) S1) =O
Molecular Formula
C13H15N3O2S
Molecular Weight
277.3421
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
Acetamide, N- (4-acetyl-4,5-dihydro-5-methyl-5-phenyl-1,3,4-thiadiazol-2-yl) -
Available Sizes
Frequently Asked Questions
Explore Other Products
Browse additional items from our catalog
ELOVL5, CT (ELOVL5, ELOVL2, Elongation of very long chain fatty acids protein 5, 3-keto acyl-CoA synthase ELOVL5, ELOVL fatty acid elongase 5, Fatty acid elongase 1) (MaxLight 550)
ELOVL5, CT (ELOVL5, ELOVL2, Elongation of very long chain fatty acids protein 5, 3-keto acyl-CoA synthase ELOVL5, ELOVL fatty acid elongase 5, Fatty acid elongase 1) (MaxLight 550)
UCP1/3 Recombinant Antibody, AbBy Fluor™ 350 Conjugated
WDFY4 CRISPRa sgRNA lentivector (set of three targets)(Mouse)
Recombinant Human N6AMT2 Protein - (Dry Ice)