目錄:MedChemExpress LLC>>生化試劑>> Niraparib (R-enantiomer) | MCE
CAS | 1038915-58-0 | 純度 | 99.69% |
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分子量 | 320.39 | 分子式 | C??H??N?O |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 2 mg |
貨號 | HY-10619D | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 1038915-58-0
產(chǎn)品活性:Niraparib R-enantiomer (MK-4827 R-enantiomer) is an excellent PARP1 inhibitor with IC50 of 2.4 nM.
研究領(lǐng)域:Cell Cycle/DNA Damage | Epigenetics
作用靶點:PARP
In Vitro: Niraparib R-enantiomer (MK-4827 R-enantiomer) resolution of Niraparib R-enantiomer give compounds Niraparib R-enantiomer and Niraparib S-enantiomer, both showing excellent inhibition of PARP-1. Niraparib R-enantiomer has somewhat lower in vitro metabolic clearance than the Niraparib S-enantiomer in rat liver microsomes, but Niraparib S-enantiomer is more potent in cell based assays (PARylation EC50, Niraparib R-enantiomer=30 nM, Niraparib S-enantiomer=4.0 nM; BRCA1-HeLa CC50, Niraparib R-enantiomer=470, Niraparib S-enantiomer=34 nM). Given this improved potency and similar in vitro turnover in human liver microsomes (HLM Clint, Niraparib R-enantiomer=4, Niraparib S-enantiomer=3 μL/min/mgP), Niraparib S-enantiomer (Niraparib) is focused on.
相關(guān)產(chǎn)品:Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Epigenetics Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Anti-Breast Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Targeted Diversity Library | Heterocyclic Compound Library | iRucaparib-AP6 | Rucaparib monocamsylate | AZD-2461 | RBN-2397 | Rucaparib acetate | Niraparib tosylate | Olaparib-d8 | G007-LK | Basroparib | Anticancer agent 64 | UPF 1069 | Talazoparib tosylate | BPA-B9 | MSC2504877 | Oxychlororaphine | PROTAC PARP1 degrader | 5,7-Dihydroxychromone | PARP1-IN-5 | OUL232 | Stenoparib | PI-1840 | PARP1-IN-11 | 3-Aminobenzamide | PARP1-IN-6 | OM-153 | BRCA1-IN-2 | PARP-2-IN-1 | JQAD1 | Benzamide-15N
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