UNC1999
CAS No. 1431612-23-5
UNC1999 ( UNC1999 | UNC 1999 | UNC-1999 )
产品货号. M11830 CAS No. 1431612-23-5
UNC1999 是一种有效的、口服生物可利用的、选择性的 EZH2 和 EZH1 抑制剂,在无细胞测定中 IC50 分别为 2 nM 和 45 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥356 | 有现货 |
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| 5MG | ¥527 | 有现货 |
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| 10MG | ¥794 | 有现货 |
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| 25MG | ¥1515 | 有现货 |
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| 50MG | ¥2446 | 有现货 |
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| 100MG | ¥4398 | 有现货 |
|
| 500MG | ¥9639 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称UNC1999
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述UNC1999 是一种有效的、口服生物可利用的、选择性的 EZH2 和 EZH1 抑制剂,在无细胞测定中 IC50 分别为 2 nM 和 45 nM。
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产品描述UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively, showing >1000-fold selectivity over a broad range of epigenetic and non-epigenetic targets.
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体外实验UNC1999, the first orally bioavailable inhibitor that has high in vitro potency for wild-type and mutant EZH2 as well as EZH1, a closely related H3K27 methyltransferase that shares 96% sequence identity with EZH2 in their respective catalytic domains. UNC1999 is highly selective for EZH2 and EZH1 over a broad range of epigenetic and non-epigenetic targets, competitive with the cofactor SAM, and non-competitive with the peptide substrate. UNC1999 has Ki values of 4,700 nM, 65 nM, 300 nM, and 1,500 nM for sigma1, sigma2, histamine H3, and NET, respectively. NC1999 selectively kills DB cells, a DLBCL cell line with the EZH2 Y641N mutation. UNC1999 displays a concentration- and time-dependent inhibition of DB cell proliferation (EC50=633±101 nM (n=3)).
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体内实验A single intraperitoneal (IP) injection of UNC1999 at 15, 50, or 150 mg/kg achieved high Cmax (9,700-11,800 nM) and exhibited dose linearity in male Swiss albino mice. Both the 150 and 50 mg/kg IP doses resulted in the plasma concentrations of UNC1999 above its cellular IC50 over the entire 24 h period while the 15 mg/kg IP dose led to the plasma concentrations of UNC1999 above its cellular IC50 for approximately 12 h. We next examined whether UNC1999 is orally bioavailable and are pleased to find that a single 50 mg/kg oral dose of UNC1999 achieved high Cmax (4,700 nM) and good exposure levels in male Swiss albino mice. The plasma concentrations of UNC1999 are maintained above its cellular IC50 for approximately 20 h following this single oral dose. It is worth noting that all doses including the 150 mg/kg IP dose are well tolerated by all test mice, and no adverse effects are observed.
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同义词UNC1999 | UNC 1999 | UNC-1999
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通路Chromatin/Epigenetic
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靶点HMTase
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受体EZH1| EZH2
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研究领域Cancer
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适应症——
化学信息
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CAS Number1431612-23-5
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分子量569.74
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分子式C33H43N7O2
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纯度>98% (HPLC)
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溶解度Ethanol: 100 mg/mL (175.51 mM); DMSO: 100 mg/mL (175.51 mM)
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SMILESO=C(NCC1=C(CCC)C=C(C)NC1=O)C2=C3C(N(C(C)C)N=C3)=CC(C4=CC=C(N5CCN(C(C)C)CC5)N=C4)=C2
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化学全称1-isopropyl-6-(6-(4-isopropylpiperazin-1-yl)pyridin-3-yl)-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-1H-indazole-4-carboxamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Konze KD, et al. ACS Chem. Biol. 2013, 8 (6), 1324–1334.
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