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目錄:MedChemExpress LLC>>生化試劑>> Atuveciclib Racemate | MCE

Atuveciclib Racemate | MCE
  • Atuveciclib Racemate | MCE
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更新時間:2023-06-28 09:24:21瀏覽次數(shù):150評價

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CAS 1414943-88-6 純度 98.48%
分子量 387.43 分子式 C??H??FN?O?S
供貨周期 現(xiàn)貨 規(guī)格 5 mg
貨號 HY-12871 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
Atuveciclib Racemate | MCEAtuveciclib Racemate (BAY-1143572 Racemate) is the racemate mixture of Atuveciclib. Atuveciclib is a potent and highly selective, oral <b>P-TEFb</b>/<b>CDK9</b> inhibitor which supresses <b>CDK9</b>/<b>CycT1</b> with an <b>IC<sub>50</sub></b> of 13 nM.

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Atuveciclib Racemate

CAS No. : 1414943-88-6

產(chǎn)品活性:Atuveciclib Racemate (BAY-1143572 Racemate) is the racemate mixture of Atuveciclib. Atuveciclib is a potent and highly selective, oral P-TEFb/CDK9 inhibitor which supresses CDK9/CycT1 with an IC50 of 13 nM.

研究領(lǐng)域:Cell Cycle/DNA Damage

作用靶點:CDK

In Vitro: Atuveciclib (BAY-1143572) inhibits the proliferation of 7 MLL-rearrangements positive and negative AML cell lines with a median IC50 of 385 nM (range 230-1100 nM) and induces apoptosis. Atuveciclib (BAY-1143572) has potent and highly selective PTEFb-kinase inhibitory activity in the low nanomolar range against PTEFb/CDK9 and an at least 50-fold selectivity against other CDKs. Atuveciclib (BAY-1143572) shows a favorable selectivity against a panel of non-CDK kinases. It shows broad antiproliferative activity against a panel of tumor cell lines with sub-micromolar IC50 values. The concentration-dependent inhibition of the phosphorylation of the RNA polymerase II and downstream reduction of MYC mRNA and protein levels is observed.

In Vivo: Atuveciclib (BAY-1143572) exhibits single agent efficacy at tolerated doses in 4 out of 5 AML xenograft tumor models in mice and in 2 out of 2 AML xenograft tumor models in rats upon once daily oral administration. Partial or even complete remissions could be achieved in several models.The inhibition of MYC mRNA is also observed in blood cells of Atuveciclib (BAY-1143572)-treated rats indicating the potential clinical utility of MYC in blood cells as a pharmacodynamic marker in clinical development. The in vivo efficacy of Atuveciclib (BAY-1143572) is significantly enhanced in combination with several chemotherapeutics in different solid tumor models.

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