AT 7519 mesylate
Data Sheet
For research use only. Not for human use.
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| CAS No. | 902135-89-1 | Cat. No. | BCP02120 |
| Name | AT 7519 mesylate | ||
| Synonyms | AT-7519 mesylate;AT7519 mesylate;AT7519M;AT-7519M;AT 7519M; | ||
| SMILES | |||
| Chemical Name | |||
| Formula | C16H17Cl2N5O2.CH4O3S | M. Wt | 478.35 |
| Purity | 98% | Storage | Store at 4-8°C |
| Description | AT7519M selectively binds to and inhibits cyclin dependent kinases (CDKs), which may result in cell cycle arrest, induction of apoptosis, and inhibition of tumor cell proliferation. AT7519 is inactive against all non-CDK kinases with the exception of GSK3β (IC50 = 89 nM). AT7519 shows potent antiproliferative activity in a variety of human tumor cell lines with IC50 values ranging from 40 nM for MCF-7 to 940 nM for SW620 consistent with the inhibition of CDK1 and CDK2. AT7519 induces dose-dependent cytotoxicity in multiple myeloma (MM) cell lines with IC50 values ranging from 0.5 to 2 μM at 48 hours, with the most sensitive cell lines being MM.1S (0.5 μM) and U266 (0.5 μM) and the most resistant MM.1R (>2 μM). It does not induce cytotoxicity in peripheral blood mononuclear cells (PBMNC). AT7519 partially overcomes the proliferative advantage conferred by IL6 and IGF-1 as well as the protective effect of bone marrow stromal cells (BMSCs). AT7519 induces rapid dephosphorylation of RNA pol II CTD at serine 2 and serine 5 sites, and leads to the inhibition of transcription, partially contributing to AT7519 induced cytotoxicity of MM cells. | ||
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