2-BFI hydrochloride structure
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Common Name | 2-BFI hydrochloride | ||
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| CAS Number | 89196-95-2 | Molecular Weight | 222.67 | |
| Density | N/A | Boiling Point | 348.1ºC at 760 mmHg | |
| Molecular Formula | C11H11ClN2O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 164.4ºC | |
Use of 2-BFI hydrochlorideRX 801077 hydrochloride (2 BFI) is a selective imidazoline I2 receptor (I2R) agonist with a Ki value of 70.1 nM. RX 801077 hydrochlorideshows anti-inflammation and neuroprotection. RX 801077 hydrochloride has the potential for the research of traumatic brain injury (TBI)[1][2]. |
| Name | 2-(1-benzofuran-2-yl)-4,5-dihydro-1H-imidazole,hydrochloride |
|---|---|
| Synonym | More Synonyms |
| Description | RX 801077 hydrochloride (2 BFI) is a selective imidazoline I2 receptor (I2R) agonist with a Ki value of 70.1 nM. RX 801077 hydrochlorideshows anti-inflammation and neuroprotection. RX 801077 hydrochloride has the potential for the research of traumatic brain injury (TBI)[1][2]. |
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| Related Catalog | |
| Target |
Ki: 70.1 nM (imidazoline I2 receptor)[1] |
| In Vivo | RX 801077 hydrochloride (5、10、20 mg/kg;腹腔注射;每天两次,持续 3 天) 在创伤性脑损伤大鼠模型中抑制 NLRP3 炎性体诱导的炎症和坏死性凋亡[2]。 Animal Model: 280-300 g, Male adult Sprague-Dawley rats (TBI model)[2] Dosage: 5, 10, 20 mg/kg Administration: I.p.; twice daily for 3 days Result: Attenuated neurological deficits, brain edema, BBB permeability and cortical tissue loss in a rat model of TBI, reduced microglial activation, neutrophil infiltration, and proinflammatory cytokine IL-1β secretion, reduced the expression of RIP1 and RIP3 in neurons in the pericontusional cortex. |
| References |
| Boiling Point | 348.1ºC at 760 mmHg |
|---|---|
| Molecular Formula | C11H11ClN2O |
| Molecular Weight | 222.67 |
| Flash Point | 164.4ºC |
| Exact Mass | 222.05600 |
| PSA | 37.53000 |
| LogP | 2.34900 |
| InChIKey | RFNFFVDVGWOSNZ-UHFFFAOYSA-N |
| SMILES | Cl.c1ccc2oc(C3=NCCN3)cc2c1 |
| HS Code | 2934999090 |
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| HS Code | 2934999090 |
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| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Name: Presynaptic alpha-2 adrenergic receptor agonistic activity in mouse vas deferens rela...
Source: ChEMBL
Target: Alpha-2B adrenergic receptor
External Id: CHEMBL646768
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Name: Ability to antagonize the inhibitory effect of clonidine on the mouse vas deferens is...
Source: ChEMBL
Target: Alpha-2B adrenergic receptor
External Id: CHEMBL646770
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Name: Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VER...
Source: ChEMBL
Target: Severe acute respiratory syndrome coronavirus 2
External Id: CHEMBL4513082
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|
Name: Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Cac...
Source: ChEMBL
Target: Severe acute respiratory syndrome coronavirus 2
External Id: CHEMBL4303805
|
|
Name: Cell-based high throughput primary assay to identify activators of GPR151
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id: GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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Name: SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response f...
Source: ChEMBL
Target: Replicase polyprotein 1ab
External Id: CHEMBL4495582
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|
Name: Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
Source: 23265
External Id: IucA Pilot Assay Tocris Library
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Name: Agonism in vitro at Alpha-1 adrenoceptor determined in rat anococcygeus preparation.
Source: ChEMBL
Target: Alpha-1A adrenergic receptor
External Id: CHEMBL647164
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|
Name: Enzymatic assay of human HDAC6 with commercial peptide substrate
Source: ChEMBL
Target: Histone deacetylase 6
External Id: CHEMBL4808149
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|
Name: Enzymatic assay of human HDAC6 with custom peptide substrate
Source: ChEMBL
Target: Histone deacetylase 6
External Id: CHEMBL4808150
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| 2-BFI hydrochloride |