| Size | Price | Stock |
|---|---|---|
| 100 mg | Get quote | |
| 250 mg | Get quote | |
| 500 mg | Get quote | |
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| Cat. No. : | HY-117612 |
| M.Wt: | 466.15 |
| Formula: | C17H10Br2N2O2S |
| Purity: | >98 % |
| Solubility: |
KS-99 is a dual inhibitor with both tubulin polymerization inhibitory activity and Akt pathway inhibitory activity. KS-99 inhibits cancer cell proliferation and induces cancer cell apoptosis. KS-99 can be used in research related to colorectal cancer, breast cancer, lung epithelial cancer and melanoma[1].
In Vitro:KS-99 (Compound 11) (0.5-50 μM; 48 h) potently inhibits the viability of HT29, A549 and UACC903 cancer cells, with IC50 values of 1.14 μM, 2.53 μM and 2.23 μM, respectively; it shows significantly lower activity against MCF-7 cells and exhibits low toxicity toward normal MEF cells after 48 h of treatment[1].
KS-99 (1.25-5.0 μM; 24 h) induces dose-dependent apoptosis in human colon cancer cell line HT29, with 66.98% of cells undergoing apoptosis after treatment with 5.0 μM for 24 h[1].
KS-99 (1.25-5.0 μM; 24 h) dose-dependently activates caspase-3/7 in human colon cancer cell line HT29, confirming that it induces the apoptotic pathway[1].
KS-99 (5 μM; 48 h) induces DNA fragmentation in human colon cancer cell line HT29[1].
KS-99 (1-2 μM; 24 h) downregulates the total Akt protein level in human HT29 colon cancer cells, and completely abolishes Akt phosphorylation following 24 h of treatment at concentrations of 1 μM and 2 μM, acting as a potent inhibitor of the Akt pathway[1].
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