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MedChemExpress (M

CAS	220127-57-1	純度	99.98%
分子量	589.71	分子式	C??H??N?O?S
供貨周期	現(xiàn)貨	規(guī)格	10 mM * 1 mL
貨號	HY-50946	應用領域	醫(yī)療衛(wèi)生,化工,生物產業(yè),制藥

Imatinib Mesylate (STI571 Mesylate) 是一種酪氨酸激酶抑制劑，可抑制 c-Kit，Bcr-Abl 和 PDGFR (IC50=100 nM)。

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Imatinib Mesylate

CAS No. : 220127-57-1

MCE 國際站：Imatinib Mesylate

產品活性：Imatinib Mesylate (STI571 Mesylate) 是一種酪氨酸激酶抑制劑，可抑制 c-Kit，Bcr-Abl 和 PDGFR (IC₅₀=100 nM)。

研究領域：Protein Tyrosine Kinase/RTK | Autophagy

作用靶點：c-Kit | Bcr-Abl | PDGFR | Autophagy

In Vitro: Imatinib (STI571) Mesylate inhibits c-Kit autophosphorylation, activation of MAPK, and activation of Akt without altering total protein levels of c-kit, MAPK, or Akt. The concentration that produces 50% inhibition for these effects is approximately 100 nM. Imatinib (STI571) mesylate is very effective (in vitro IC₅₀ of 25 nM) against the chronic myeloid leukemia-causing kinase Bcr-Abl. Imatinib also efficiently inhibits Kit (in vitro IC₅₀, 410 nM) and PDGFR (in vitro IC₅₀, 380 nM). Imatinib (STI571) mesylate is a multi-target inhibitor of v-Abl, c-Kit and inhibits Bcr/Abl, v-Abl, Tel/Abl, the native PDGFβ receptor, and c-Kit, but it does not inhibit Src family kinases, c-Fms, Flt3, the EGFR or multiple other tyrosine kinases. Imatinib inhibits tyrosine phosphorylation and cell growth of Ba/F3 cells expressing Bcr/Abl, Tel/Abl, Tel/PDGFβR, and Tel/Arg with an IC₅₀ of approximately 0.5 μM in each case, but it has no effect on untransformed Ba/F3 cells growing in IL-3 or on Ba/F3 cells transformed by Tel/JAK2. Imatinib mesylate selectively inhibits the activity of Bcr/Abl, c-Kit and PDGFR kinases. Imatinib mesylate reveals distinct and rapid antileukemic activity in chronic myelogenous leukemia (CML) and Philadelphia-positive (Ph⁺) acute lymphoblastic leukemia (ALL).

In Vivo: Animals treated with Imatinib Mesylate show a decrease of mean body weight throughout the whole study. Body weight loss is noticeable in mice from groups that receive chemotherapy and the vitamin D analog combined treatment. The body weight decrease of mice treat with both combined Imatinib mesylate and PRI-2191 is the highest (15%) on Day 22 of the experiment, but after that day, mice start to recover. In a rat Ischemia/reperfusion injury (IRI) model, Imatinib mesylate attenuates lung injury by an antipermeability and antiinflammatory effect. The delivery and function of Imatinib mesylate in the lung is also confirmed in this model.