2-BFI hydrochloride
目录号 : GC115882-BFI hydrochloride是高亲和力、选择性的咪唑啉I2受体(I2R)激动剂,Ki值为70.1nM。
Cas No.:89196-95-2
Sample solution is provided at 25 µL, 10mM.
2-BFI hydrochloride is a high-affinity, selective agonist of the imidazoline I2 receptor (I2R) with a Ki of 70.1nM[1]. I2R is an allosteric binding site on monoamine oxidase-B that modulates neurotransmitter metabolism and neuroprotection[2]. 2-BFI hydrochloride is commonly used in studies of neuroprotection, anti-inflammation, and traumatic brain injury (TBI)[3].
In vitro, treatment of cultured rat cortical neurons with 2-BFI hydrochloride (30-1000µM; 2-3min) selectively inhibits NMDA-evoked currents[4]. Treatment of HT-29 and HCT-116 colorectal cancer cells with 2-BFI hydrochloride (250μM; 24-48h) significantly potentiated hydroxychloroquine cytotoxicity, elevated ROS, increased early/late apoptosis, and blocked autophagic flux[5].
In vivo, 2-BFI hydrochloride (3mg/kg; i.p.; 3 days) reduced cerebral infarct volume, improved motor deficits in distal middle cerebral artery occlusion (dMCAO) rats, inhibited mTOR phosphorylation and shifted cytokine balance toward anti-inflammation[6]. 2-BFI hydrochloride (10mg/kg; i.p.; twice daily for 7 days) reversed CCI-induced mechanical and thermal hypersensitivity, and reduced spinal Iba-1 and GFAP expression and TNF-α levels in neuropathic pain rats[7].
References:
[1] Carpéné C, Collon P, Remaury A, et al. Inhibition of amine oxidase activity by derivatives that recognize imidazoline I2 sites. J Pharmacol Exp Ther. 1995;272(2):681-688.
[2] Li JX. Imidazoline I2 receptors: An update. Pharmacol Ther. 2017;178:48-56.
[3] Ni H, Rui Q, Lin X, Li D, Liu H, Chen G. 2-BFI Provides Neuroprotection Against Inflammation and Necroptosis in a Rat Model of Traumatic Brain Injury. Front Neurosci. 2019;13:674.
[4] Xu S, Chen J, Xu C, et al. 2-BFI protects against ischemic stroke by selectively acting on NR2B-containing NMDA receptors. Brain Res. 2024;1845:149284.
[5] Kowalski S, Wityk P, Raczak-Gutknecht J, Olszewska A, Zmijewski M, Kocic I. The imidazoline I2 receptor agonist 2-BFI enhances cytotoxic activity of hydroxychloroquine by modulating oxidative stress, energy-related metabolism and autophagic influx in human colorectal adenocarcinoma cell lines. Eur J Pharmacol. 2025;996:177590.
[6] Cheng Y, Zhang W, Cao W, et al. 2-BFI attenuates ischemic injury by modulating mTOR signaling and neuroinflammation in rats. Neurosci Lett. 2021;750:135766.
[7] Siemian JN, LaMacchia ZM, Spreuer V, et al. The imidazoline I2 receptor agonist 2-BFI attenuates hypersensitivity and spinal neuroinflammation in a rat model of neuropathic pain. Biochem Pharmacol. 2018;153:260-268.
2-BFI hydrochloride是高亲和力、选择性的咪唑啉I2受体(I2R)激动剂,Ki值为70.1nM[1]。I2R是单胺氧化酶B上的变构结合位点,可调节神经递质代谢和神经保护[2]。2-BFI hydrochloride常用于神经保护、抗炎和创伤性脑损伤(TBI)等研究[3]。
在体外,2-BFI hydrochloride(30-1000µM;2-3分钟)可选择性抑制培养大鼠皮层神经元中NMDA诱发的电流[4]。2-BFI hydrochloride(250µM;24-48小时)显著增强HT-29和HCT-116结肠癌细胞中羟氯喹的细胞毒性,升高活性氧(ROS)水平,增加早期/晚期凋亡,并阻断自噬通量[5]。
在体内,2-BFI hydrochloride(3mg/kg;腹腔注射;连续3天)可减少远端大脑中动脉闭塞(dMCAO)大鼠的脑梗死体积,改善运动功能缺陷,抑制mTOR磷酸化,并使细胞因子平衡向抗炎方向转变[6]。2-BFI hydrochloride(10mg/kg;腹腔注射;每日两次,连续7天)可逆转慢性缩窄性损伤(CCI)诱导的机械性和热痛觉过敏,并降低神经病理性疼痛大鼠脊髓中Iba-1和GFAP的表达及TNF-α水平[7]。
| Cell experiment [1]: | |
Cell lines | Human colorectal adenocarcinoma cell lines HT-29 and HCT-116 |
Preparation Method | Human colorectal adenocarcinoma cell lines HT-29 and HCT-116 were cultured in McCoy’s 5A Medium (modified), with L-Glutamine, supplemented with 10% fetal bovine serum, 100units/mL penicillin and 100μg/mL streptomycin. Cell cultures were incubated in a humidified atmosphere of 95% air and 5% CO2 at 37℃. 2-BFI hydrochloride was dissolved in water as a 10mM masterbatch and storage at −80℃ refrigerator. HT-29 and HCT-116 cells were seeded in triplicate on 96-well plates at a density of 10×103cells/100μL. The next day, cells were exposed to 2-BFI (250μM) and/or HCQ for 24h and 48h. The MTT assay was used to measure cell viability according to the commercially available protocol. The generation of intracellular ROS level and apoptosis detection were measured using flow cytometry technique. The Autophagy Kit was used to monitor autophagic flux. |
Reaction Conditions | 250μM; 24-48h |
Applications | Treatment of HT-29 and HCT-116 colorectal cancer cells with 2-BFI hydrochloride significantly potentiated hydroxychloroquine cytotoxicity, elevated ROS, increased early/late apoptosis, and blocked autophagic flux. |
| Animal experiment [2]: | |
Animal models | Male adult Sprague-Dawley rats |
Preparation Method | Male adult (2-month-old, 250-300g) Sprague-Dawley rats were housed in a temperature (23±1℃) and humidity (50%) controlled animal facility with 12:12h light–dark cycle. Food and water were available ad libitum. Focal cerebral ischemic stroke model was established by permanent distal middle cerebral artery occlusion (dMCAO) method. Immediately following dMCAO, rats were randomly selected and administered 2-BFI hydrochloride (3mg/kg) or saline intraperitoneally. Rats undergo neurobehavioral tests to evaluate functional outcome 1 and 3 days after ischemia. The modified beam balance test was used to assess the motor balance and coordination in ischemic rats, especially in the hindlimb. The brains of rat were removed 3 days after ischemia, 2mm coronal sections were cut and stained with 2,3,5-triphenyltetrazolium hydrochloride (TTC). Western blotting procedures were performed to assess the profile of mTOR activation. To test the inflammatory response after 2BFI treatment, colorimetric ELISA kits were used to detect the following cytokines in brain protein extract: IL-10,TNF-α, TGF-β. |
Dosage form | 3mg/kg; i.p.; 3 days |
Applications | 2-BFI hydrochloride reduced cerebral infarct volume, improved motor deficits in dMCAO rats, inhibited mTOR phosphorylation and shifted cytokine balance toward anti-inflammation. |
References: | |
| Cas No. | 89196-95-2 | SDF | |
| 化学名 | 2-(benzofuran-2-yl)-4,5-dihydro-1H-imidazole hydrochloride | ||
| Canonical SMILES | C12=CC=CC=C1OC(C3=NCCN3)=C2.Cl | ||
| 分子式 | C11H11ClN2O | 分子量 | 222.67 |
| 溶解度 | 22.2mg/ml in Water | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg |
| 1 mM | 4.491 mL | 22.4548 mL | 44.9095 mL |
| 5 mM | 898.2 μL | 4.491 mL | 8.9819 mL |
| 10 mM | 449.1 μL | 2.2455 mL | 4.491 mL |
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