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LY2334737

LY2334737

产品编号 T4061   CAS 892128-60-8

LY2334737 是一种具有口服活性的 Gemcitabine 的前药,也是核苷类似物。它抑制肠道病毒 A71 感染,有抗病毒和抗癌活性。

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LY2334737 Chemical Structure
LY2334737, CAS 892128-60-8
规格 价格/CNY 货期 数量
1 mg ¥ 833 现货
2 mg ¥ 1,220 现货
5 mg ¥ 1,830 现货
10 mg ¥ 2,790 现货
25 mg ¥ 4,650 现货
50 mg ¥ 6,630 现货
100 mg ¥ 8,850 现货
1 mL * 10 mM (in DMSO) ¥ 1,560 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: LY2334737 (T4061)
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生物活性
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参考文献
产品描述 LY2334737 is an orally available prodrug of gemcitabine with antineoplastic activity.
体外活性 Five cell lines that express CES2 responded to LY2334737treatment. LY2334737 was less cytotoxic to a SK-OV-3 CES2 knockdown than parental cells. The drug response of CES2-transfected HCT-116 cells correlated with CES2 expression level. Bystander studies showed statistically greater PC-3-GFP growth inhibition by LY2334737 when cells were cocultured with CES2 and not mock transfectants [1].
体内活性 Oral treatment of xenograft models with 3.2 mg/kg LY2334737 once a day for 21 days showed greater tumor growth inhibition of CES2 transfectant than the mock transfectant (P ≤ 0.001) [1]. The MTD was 40 mg LY2334737. Fatigue was the most frequent DLT for LY2334737monotherapy (4 patients) followed by elevated transaminase levels (2 patients), both observed at the 40- to 50-mg dose levels. Among the 10 patients in the combination arm, 2 had DLTs at the 40-mg dose level. These were fatigue and elevated liver enzyme levels [2]. Metronomic LY2334737 administration caused increased blood flow in luciferase-tagged LM2-4 tumor xenografts, and this effect, readily measured using contrast micro-ultrasound, coincided with a relative increase in tumor bioluminescence [3].
分子量 389.39
分子式 C17H25F2N3O5
CAS No. 892128-60-8

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 45 mg/mL (115.56 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.5681 mL 12.8406 mL 25.6812 mL 64.203 mL
5 mM 0.5136 mL 2.5681 mL 5.1362 mL 12.8406 mL
10 mM 0.2568 mL 1.2841 mL 2.5681 mL 6.4203 mL
20 mM 0.1284 mL 0.642 mL 1.2841 mL 3.2101 mL
50 mM 0.0514 mL 0.2568 mL 0.5136 mL 1.2841 mL
100 mM 0.0257 mL 0.1284 mL 0.2568 mL 0.642 mL

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TargetMol Library Books参考文献

1. Pratt SE, et al. Human carboxylesterase-2 hydrolyzes the prodrug of gemcitabine (LY2334737) and confers prodrug sensitivity to cancer cells. Clin Cancer Res. 2013 Mar 1;19(5):1159-68. 2. Koolen SL, et al. Phase I study of Oral gemcitabine prodrug (LY2334737) alone and in combination with erlotinib in patients with advanced solid tumors. Clin Cancer Res. 2011 Sep 15;17(18):6071-82. 3. Francia G, et al. Low-dose metronomic oral dosing of a prodrug of gemcitabine (LY2334737) causes antitumor effects in the absence of inhibition of systemic vasculogenesis. Mol Cancer Ther. 2012 Mar;11(3):680-9. 4. Cai Y, Zhou H, Zhu Y, et al. Elimination of senescent cells by β-galactosidase-targeted prodrug attenuates inflammation and restores physical function in aged mice[J]. Cell Research. 2020: 1-16.

TargetMol Library Books文献引用

1. Cai Y, Zhou H, Zhu Y, et al. Elimination of senescent cells by β-galactosidase-targeted prodrug attenuates inflammation and restores physical function in aged mice. Cell Research. 2020: 1-16.
Dacarbazine 5-BrdU 5-Ethynyluridine 8-Azaguanine Gemcitabine elaidate 3-Deazauridine Decitabine Carmofur

相关化合物库

该产品包含在如下化合物库中:
抗癌临床化合物库 药物功能重定位化合物库 抗癌药物库 抗癌活性化合物库 抗病毒库 经典已知活性库 已知活性化合物库 共价抑制剂库 口服活性化合物库 NO PAINS 化合物库

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母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

LY2334737 892128-60-8 Cell Cycle/Checkpoint DNA Damage/DNA Repair Microbiology/Virology Others Nucleoside Antimetabolite/Analog Virus Protease anticancer LY-2334737 HEV Gemcitabine HEVs HRVs EV-A71 Rhinovirus inhibit LY 2334737 Enterovirus HRV orally antiviral Inhibitor inhibitor

 

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