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Imatinib
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CAS No. | 152459-95-5 | Cat. No. | BCP01542 |
Name | Imatinib | ||
Synonyms | STI571;Glivec;STI-571;STI 571;STI571; | ||
SMILES | |||
Chemical Name | |||
Formula | C29H31N7O | M. Wt | 493.6 |
Purity | 98% | Storage | Store at 4-8°C |
Description | In vitro assays for inhibition of a panel of tyrosine and serine/threonine protein kinases show that Imatinib inhibits the v-Abl tyrosine kinase and PDGFR potently with an IC50 of 0.6 and 0.1 μM, respectively.Imatinib inhibits the SLF-dependent activation of wild-type c-kit kinase activity with a IC50 for these effects of approximately 0.1 μM, which is similar to the concentration required for inhibition of PDGFR. Imatinib exhibits growth-inhibitory activity on the human bronchial carcinoid cell line NCI-H727 and the human pancreatic carcinoid cell line BON-1 with an IC50 of 32.4 and 32.8 μM, respectively. A recent study shows that Imatinib has the potential to exert its antileukemia effects in chronic myelogenous leukemia by down-regulating hERG1 K(+) channels, which are highly expressed in leukemia cells and appear of exceptional importance in favoring leukemogenesis. |
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