Furafylline

目录号: GC32855纯度: >99.50%同义词: 呋拉茶碱
Furafylline,作为治疗哮喘的长效茶碱替代品,是甲基黄嘌呤衍生物。

Furafylline
Cas No.: 80288-49-9
规格价格库存数量操作
5mg¥1,526.00现货
1
10mg¥2,289.00现货
1
25mg¥4,004.00现货
1
10mM (in 1mL DMSO)¥1,679.00现货
1

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产品描述 Description

Furafylline, as a long-acting replacement for theophylline in the treatment of asthma, is a methylxanthine derivative[1].

In vitro efficacy test it shown that Furafylline was a potent, non-competitive inhibitor of high affinity phenacetin O-deethylase activity of microsomal fractions of human liver, a reaction catalysed by P450IA2, with an IC50 value of 0.07 µM[1]. In vitro, prior to the initiation of the reaction by the addition of substrate, preincubating microsomes with 10 µM furafylline for 10 min in the presence of NADPH, resulted in marked inhibition of 1A2 activity[2]. In vitro, furafylline has inhibition agaisnt NCMN-O-dealkylation in cynomolgus monkey liver microsomes (CyLM), beagle dog liver microsomes (DLM), minipig liver microsomes (PLM), mouse liver microsomes (MLM) and rat liver microsomes (RLM) with IC50 of 56.36 µM, 26.77 µM, 14.61 µM, 5.73 µM and 1.98 µM, respectively[3].

In vivo test it demonstrated that humanized-liver mice were treated with furafylline (daily oral doses of 13 mg/kg for 3 days) decreased the mean values of the areas under the plasma concentration versus time curves and the maximum concentrations for o-hydroxyphenylacetic acid[4]. In vivo efficacy test it exhibited that beagle dogs were administrated 0.5 and 10 mg/kg orally observed an elimination half-life 2-10 times longer than that of theophylline in a dose-dependent kinetically[5].

References:

Sesardic D, et al. Furafylline is a potent and selective inhibitor of cytochrome P450IA2 in man. Br J Clin Pharmacol. 1990 Jun;29(6):651-63.

Clarke SE, et al. Characterization of the inhibition of P4501A2 by furafylline. Xenobiotica. 1994 Jun;24(6):517-26.

Dai Z, et al. Interspecies Variation in NCMN-O-Demethylation in Liver Microsomes from Various Species. Molecules. 2019 Jul 30;24(15):2765.

Miura T, et al. Roles of human cytochrome P450 1A2 in coumarin 3,4-epoxidation mediated by untreated hepatocytes and by those metabolically inactivated with furafylline in previously transplanted chimeric mice. J Toxicol Sci. 2021;46(11):525-530.

Segura J, et al. Some pharmacokinetic characteristics of furafylline, a new 1,3,8-trisubstituted xanthine. J Pharm Pharmacol. 1986 Aug;38(8):615-8.

实验参考方法 Experimental Reference Method

Cell experiment [1]:

Cell lines

human hepatocytes

Preparation Method

25 µM; for 2.2 h at 37 °C

Reaction Conditions

Sunitinib (10 µM) was incubated with cryopreserved CYP3A5-genotyped human hepatocytes (0.5 × 106 cells/mL in KHB) from 12 individual donors in suspension for 2.2 h at 37 °C. For each donor, incubations were conducted in at least triplicate (three wells per condition). To examine the effect of P450 1A2 inhibitor furafylline (25 µM) on metabolite formation, hepatocytes were coincubated with sunitinib and furafylline in replicates of 2-4 wells per donor, except for donor ZUJ.

Applications

Furafylline reduced M3 (defluorosunitinib) and M5 (glutathione conjugate) formation by 73.2% ± 0.89% and 81.4% ± 4.84%, respectively, compared to the control. Furafylline reduced M1 (N-desethylsunitinib) formation by only 19.4% ± 5.10% .

Animal experiment [2]:

Animal models

rats

Preparation Method

10 mg/kg; p.o.

Dosage form

Rats were treated 10 mg/kg furafylline orally and test plasma levels of caffeine.

Applications

Plasma levels of caffeine are increased more than 400% in rats given furafylline (10 mg kg-1 p.o.) and caffeine (25 mg kg-1 p.o.) as compared to rats given caffeine alone.

References:

Burnham EA, et al. Interindividual Variability in Cytochrome P450 3A and 1A Activity Influences Sunitinib Metabolism and Bioactivation. Chem Res Toxicol. 2022 May 16;35(5):792-806.
TarrÚs E, et al. An animal model for the detection of drug-induced inhibition of caffeine metabolism. Methods Find Exp Clin Pharmacol. 1987 May;9(5):311-6.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
80288-49-9
同义词
呋拉茶碱
SMILES
O=C1N(C2=C(N=C(C)N2)C(N1C)=O)CC3=CC=CO3
分子式
C12H12N4O3
分子量
260.25 g/mol
溶解性
DMSO : 12.5 mg/mL (48.03 mM);Water : < 0.1 mg/mL (insoluble)
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol