L-Eflornithine monohydrochloride

目录号: PL08809 纯度: ≥98.0%
L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) 是 Eflornithine 的对映异构体。L-Eflornithine 是一种不可逆的鸟氨酸脱羧酶 (ornithine decarboxylase, ODC) 抑制剂,KD 为 1.3±0.3 μM,Kinact 为 0.15±0.03 min-1
CAS No. :69955-42-6
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中文名称
L-Eflornithine monohydrochloride
英文名称
L-Eflornithine monohydrochloride
英文别名
L-Ornithine, 2-(difluoromethyl)-, monohydrochloride;M3O9BB413G;Eflornithine hydrochloride, (S)-;FJPAMFNRCFEGSD-QYCVXMPOSA-N;alpha-difluoromethyl ornithine hydrochloride monohydrate;(+)-alpha-difluoromethylornithine monohydrochloride monohydrate;L-Eflornithine monohydrochloride
Cas No.
69955-42-6
分子式
C6H15ClF2N2O3
分子量
236.64
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
详情描述
L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) 是 Eflornithine 的对映异构体。L-Eflornithine 是一种不可逆的鸟氨酸脱羧酶 (ornithine decarboxylase, ODC) 抑制剂,KD 为 1.3±0.3 μM,Kinact 为 0.15±0.03 min-1
产品详情
L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) 是 Eflornithine 的对映异构体。L-Eflornithine 是一种不可逆的鸟氨酸脱羧酶 (ornithine decarboxylase, ODC) 抑制剂,KD 为 1.3±0.3 μM,Kinact 为 0.15±0.03 min-1
生物活性
L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) is an enantiomer of Eflornithine. L-Eflornithine is an irreversible ornithine decarboxylase (ODC) inhibitor with a K D of 1.3±0.3 μM, and a K inact of 0.15±0.03 min.
性状
Solid
IC50 & Target[1][2]
KD:1.3±0.3 μM (Ornithine decarboxylase, ODC)
体外研究(In Vitro)
Eflornithine (D/L-DFMO) is an inhibitor of ODC, the first enzyme in eukaryotic polyamine biosynthesis. Both enantiomers of Eflornithine (DFMO) irreversibly inactivate ODC. Both Eflornithine enantiomers (L-Eflornithine and D-Eflornithine) suppress ODC activity in a time- and concentration-dependent manner. The inhibitor dissociation constant (KD) values for the formation of enzyme-inhibitor complexes are 28.3±3.4, 1.3±0.3 and 2.2±0.4 μM respectively for D-Eflornithine, L-Eflornithine and Eflornithine. The inhibitor inactivation constants (Kinact) for the irreversible step were 0.25±0.03, 0.15±0.03 and 0.15±0.03 min respectively for D-Eflornithine, L-Eflornithine and Eflornithine. Treatment of human colon tumour-derived HCT116 cells with either L-Eflornithine or D- Eflornithine decreases the cellular polyamine contents in a concentration-dependent manner. T
体内研究(In Vivo)
The more potent L-Eflornithine is present at much lower concentrations in both plasma and cerebrospinal fluid (CSF) than those of the D-Eflornithine. The plasma concentrations of L-Eflornithine are on average 52% of the D-enantiomer concentrations. The typical oral clearances of L-Eflornithine and D-eflornithine are 17.4 and 8.23 liters/h, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Qu N, et al. Inhibition of human ornithine decarboxylase activity by enantiomers of difluoromethylornithine. Biochem J. 2003 Oct 15;375(Pt 2):465-70.
[2]. Jansson-L?fmark R, et al. Enantiospecific reassessment of the pharmacokinetics and pharmacodynamics of oral eflornithine against late-stage Trypanosoma brucei gambiense sleeping sickness. Antimicrob Agents Chemother. 2015 Feb;59(2):1299-307.
溶解度数据
In Vitro: DMSO : 200 mg/mL (914.79 mM; Need ultrasonic)H2O : 50 mg/mL (228.70 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Qu N, et al. Inhibition of human ornithine decarboxylase activity by enantiomers of difluoromethylornithine. Biochem J. 2003 Oct 15;375(Pt 2):465-70.
[2]. Jansson-L?fmark R, et al. Enantiospecific reassessment of the pharmacokinetics and pharmacodynamics of oral eflornithine against late-stage Trypanosoma brucei gambiense sleeping sickness. Antimicrob Agents Chemother. 2015 Feb;59(2):1299-307.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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