Benpyrine

未知

苯并吡啶

Benpyrine

B648096-5mg

5mg

≥99%

-20°C储存

超低温冰袋运输

Benpyrine is a highly specific and orally active TNF-α inhibitor with a K D value of 82.1 μM. Benpyrine tightly binds to TNF-α and blocks its interaction with TNFR1, with an IC 50 value of 0.109 µM. Benpyrine has the potential for TNF-α mediated inflammatory and autoimmune disease research In Vitro Benpyrine (5-20 µM; 14 hours; RAW264.7 cells) pretreatment results in a dose-dependent decrease in the phosphorylation of IκBα in RAW264.7 cells (stimulated with 10 ng/mL TNF-α or 1 μg/mL LPS). Benpyrine abolishes the TNF-α-induced nuclear translocation of NF-κB/p65 in RAW264.7 cells. Benpyrine only blocks cell death induced by TNF-α WT and Y 119 A, and increases the cell survival rate up to 80%. Benpyrine does not obviously affect L 57 A- and Y 59 L-induced cytotoxicity in L929 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: RAW264.7 cells Concentration: 5 µM, 10 µM, 20 µM Incubation Time: 14 hours Result: Resulted in a dose-dependent decrease in the phosphorylation of IκBα. In Vivo Benpyrine (25-50 mg/kg; oral gavage; daily; for 2 weeks; Balb/c mice) treatment significantly relieves the symptoms of collagen-induced arthritis. Benpyrine dose-dependently decreases the levels of proinflammatory cytokines, such as IFN-γ, IL-1β and IL-6, and increases the concentration of the anti-inflammatory cytokine IL-10 . Endotoxemia murine model shows that Benpyrine (25 mg/kg) could attenuate TNF-α-induced inflammation, thereby reducing liver and lung injury . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Balb/c mice (18-20 g) injected with collagen Dosage: 25 mg/kg, 50 mg/kg Administration: Oral gavage; daily; for 2 weeks Result: Relieved the symptoms of collagen-induced arthritis in mice. Form:Solid IC50& Target:KD: 82.1 μM (TNF-α)

苯吡啶是一种高度特异性和口服活性的 TNF-α 抑制剂，其 K D 值为 82.1 μM。苯吡林与 TNF-α 紧密结合，并阻断其与 TNFR1 的相互作用，其 IC 50 值为 0.109 µM。本吡啶具有抑制 TNF-α 介导的炎症反应的潜力。

2550398-89-3

C16H16N6O

308.34 g/mol

95327594

C1[C@@H](CN(C1=O)CC2=CC=CC=C2)NC3=NC=NC4=C3NC=N4

(4S)-1-benzyl-4-(7H-purin-6-ylamino)pyrrolidin-2-one

1S/C16H16N6O/c23-13-6-12(8-22(13)7-11-4-2-1-3-5-11)21-16-14-15(18-9-17-14)19-10-20-16/h1-5,9-10,12H,6-8H2,(H2,17,18,19,20,21)/t12-/m0/s1

HUWOMAVUXTXEKT-LBPRGKRZSA-N

C1C(CN(C1=O)CC2=CC=CC=C2)NC3=NC=NC4=C3NC=N4

DMSO : 12.5 mg/mL (40.54 mM; Need ultrasonic)

36240659