中文名 | 氟比洛芬 |
英文名 | (2R)-2-(3-fluoro-4-phenyl-phenyl)propanoic acid |
别名 | 氟比洛芬 R-氟比洛 (R)-氟比洛芬 R(-)氟比洛芬 (R)-2-氟比洛芬 氟比洛芬 EP标准品 (R)-(-)-2-氟-Α-甲基-4-联苯乙酸 (R)-(-)-2-氟-alpha-甲基-4-联苯乙酸 (R)-(-)-2-氟-ALPHA-甲基-4-联苯乙酸 |
英文别名 | Flurizan MPC7869 Flurbiprofen (R)-2-Flurbiprofen (2R)-2-(2-fluorobiphenyl-4-yl)propanoic acid (2R)-2-(3-fluoro-4-phenyl-phenyl)propanoic acid (R)-2-Fluoro-α-methyl-1,1'-biphenyl-4-acetic acid (R)-α-Methyl-2-fluoro-1,1'-biphenyl-4-acetic acid (R)-(-)-2-Fluoro-alpha-methyl-4-biphenylacetic acid 1,4-bis(1,1,1,2,3,3,3-heptafluoropropan-2-yl)benzene [1,1'-Biphenyl]-4-aceticacid, 2-fluoro-a-Methyl-,(aR)- (R)-(-)-2-Fluoro-alpha-methyl-4-biphenylacetic acid(Flurbiprofe [1,1'-biphenyl]-4-acetic acid, 2-fluoro-alpha-methyl-,(alphaR)- |
CAS | 51543-40-9 5104-49-4 |
EINECS | 257-264-7 |
化学式 | C15H13FO2 |
分子量 | 244.26 |
InChI | InChI=1/C12H4F14/c13-7(9(15,16)17,10(18,19)20)5-1-2-6(4-3-5)8(14,11(21,22)23)12(24,25)26/h1-4H |
密度 | 1.199±0.06 g/cm3(Predicted) |
熔点 | 110-113°C(lit.) |
沸点 | 376.2±30.0 °C(Predicted) |
闪点 | 57.7°C |
蒸汽压 | 2.84mmHg at 25°C |
溶解度 | Soluble in DMSO (50 mg/ml), methanol (50 mg/ml), ethanol (~100 mg/ml), DMF (~100 mg/ml) |
折射率 | 1.34 |
酸度系数 | 4.14±0.10(Predicted) |
存储条件 | Room Temprature |
外观 | Crystalline Powder |
颜色 | White to off-white |
MDL号 | MFCD00079303 |
体外研究 | Tarenflurbil ((R)-Flurbiprofen) can significantly reduce Aβsecretion, but at the same time, increases the level ofintracellular Aβ. The binding between [ 3 H]9-cis-RA and RXRα iscompetitively inhibited by both unlabeled (R)-Flurbiprofen and9-cis-RA. (R)-Flurbiprofen can interfere with the interactionbetween RXRα and 9-cis-retinoid acid (9-cis-RA), and that 9-cis-RAdecreases Tarenflurbil ((R)-Flurbiprofen)’s reduction of Aβsecretion. Tarenflurbil ((R)-Flurbiprofen) treatment significantlyincreases the levels of intracellular Aβ species. The wellcharacterized, nonsteroidal anti-inflammatory drug (nonsteroidalanti-inflammatory drug), Tarenflurbil ((R)-Flurbiprofen) affectsonly Aβ and not Notch β formation, indicating that secondgeneration GSMs and nonsteroidal anti-inflammatory drug-based GSMshave different modes of action regarding Notch processing. |
体内研究 | Effects of the early and late onset of treatment with Tarenflurbil((R)-Flurbiprofen) are assessed in C57BL6/J mice that develop anon-remitting form of the disease, and in SJL mice that develop arelapsing-remitting (RR)-EAE. Tarenflurbil ((R)-Flurbiprofen)completely prevents the development of clinical EAE scores inC57BL6/J mice when the treatment is started within 3 days afterimmunization. This regimen is referred to as preventive treatment.The effect is dose-dependent, and the minimum daily dose forcomplete prevention is 5 mg/kg/day. Effects of Tarenflurbil((R)-Flurbiprofen) are comparable to those of Fingolimod (FTY720,0.5 mg/kg/day), which is used as the positive control. Tarenflurbil((R)-Flurbiprofen) also significantly reduces clinical EAE scoresin C57BL6/J mice when treatment is started shortly before onset ofclinical manifestations, referred to as semi-therapeutic (10mg/kg/day) and reduces clinical scores when the treatment isinitiated after full development of the disease on day 13 (5mg/g/day). |
氟比洛芬CAS: 51543-40-9;5104-49-4原料药研发定制
2024-12-17 08:00 220.184.144.71 1次- 发布企业
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