Benoxaprofen
Based on 1 Customer Validation
Benoxaprofen (LRCL 3794) is a nonsteroidal anti-inflammatory agent that blocks the biosynthesis of inflammatory mediators such as leukotrienes and prostaglandins by inhibiting 5-LOX, PGH2 synthase and cytochrome P-450. Benoxaprofen exhibits significant toxicity: it not only alters cellular redox status, uncouples oxidative phosphorylation and disrupts calcium ion homeostasis, but also causes liver injury through the formation of covalent adducts between its active metabolites and hepatic proteins. Benoxaprofen shows strong phototoxicity under ultraviolet irradiation, and induces erythrocyte lysis, mast cell degranulation and histamine release. Benoxaprofen is widely used in studies of urticaria and related phototoxic mechanisms.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.03%
- CAS 番号: 51234-28-7
- 分子式: C16H12ClNO3
- 分子量:301.72
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保管条件:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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5-LOX |
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Cell Line
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Type | Value | Description | References |
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| Sf21 | IC50 |
175 μM
Compound: Benoxaprofen
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Inhibition of human BSEP expressed in plasma membrane vesicles of Sf21 cells assessed as inhibition of ATP-dependent [3H]taurocholate uptake
Inhibition of human BSEP expressed in plasma membrane vesicles of Sf21 cells assessed as inhibition of ATP-dependent [3H]taurocholate uptake
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[PMID: 21965623] |
| Sf21 | IC50 |
99.1 μM
Compound: Benoxaprofen
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Inhibition of Sprague-Dawley rat Bsep expressed in plasma membrane vesicles of Sf21 cells assessed as inhibition of ATP-dependent [3H]taurocholate uptake
Inhibition of Sprague-Dawley rat Bsep expressed in plasma membrane vesicles of Sf21 cells assessed as inhibition of ATP-dependent [3H]taurocholate uptake
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[PMID: 21965623] |
Benoxaprofen (0.25-2.5 mM; 10-15 min) binds to cytochrome P-450 in rat liver microsomes to form a type I spectral complex, and competitively inhibits aminopyrine demethylation with a Ki value of 0.38 mM[1].
Benoxaprofen (0.75-1.25 mM; 2-4 h) does not alter the increased L/P ratio or ALT release it induces in uninduced isolated rat hepatocytes[1].
Benoxaprofen inhibits the production of iSRS, i12-HETE and PGE2 stimulated by A-23187 in RBL-1 cells, with IC50 values of 0.4 μM, 0.45 μM, and 1.3 μM, respectively[2].
Benoxaprofen (50 μg/mL; 24 h) does not form detectable irreversible adducts with human serum albumin at pH 7.4 and 37 °C[3].
Benoxaprofen (8 μM; 10 min, irradiated) induces photolysis of human erythrocytes; hemolysis occurs faster and earlier under aerobic conditions compared with anaerobic conditions, whereas no hemolysis takes place in dark environments[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:human erythrocytes
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Concentration:8 μM
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Incubation Time:10 min; irradiated
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Result:Induced photohemolysis of human erythrocytes in a concentration-dependent manner, with faster and earlier onset of lysis under oxygenated conditions compared to anaerobic conditions; no lysis occurs in the dark.
Benoxaprofen (20-200 mg/kg; i.p.; single dose) administered intraperitoneally to male Sprague-Dawley rats results in dose-proportional liver protein adduct formation and dose-dependent covalent modification of ~70 kDa and ~110 kDa hepatic proteins at 8 h post-administration[3].
Benoxaprofen (100 mg/kg; i.p.; single dose) administered intraperitoneally to male Sprague-Dawley rats results in time-dependent covalent modification of ~70 kDa and ~110 kDa hepatic proteins detectable from 4 to 24 h post-administration[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley rat (male, 200-300 g)[3]
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Dosage:20 mg/kg
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Administration:i.v.; single bolus dose
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Result:Detectable plasma protein adducts at 1, 4, and 8 h post-administration.
Had liver protein adducts below the detection limit (~1 pmol/mg protein).
Achieved a systemic exposure (AUC0→8ₕ) of benoxaprofen glucuronide (BNX-G) of 1.98 ± 0.59 μg h/mL.
Reached a hepatobiliary exposure (Aₑ,ᵦᵢₗₑ,0→8ₕ) of BNX-G of 10.8 ± 1.4% of the dose.
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Animal Model:Sprague-Dawley rat (male, 200-300 g)[3]
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Dosage:20 mg/kg; 50 mg/kg; 100 mg/kg; 200 mg/kg
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Administration:i.p.; single dose
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Result:Exhibited dose-proportional liver protein adduct formation, with ~1.5 pmol/mg protein at 50 mg/kg, ~2.8 pmol/mg protein at 100 mg/kg, and ~6.5 pmol/mg protein at 200 mg/kg.
Showed dose-dependent covalent modification of two major liver proteins with molecular masses of ~70 kDa and ~110 kDa, with signal intensity more prominent in benoxaprofen-treated livers compared to controls.
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Animal Model:Sprague-Dawley rat (male, 200-300 g)[3]
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Dosage:100 mg/kg
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Administration:i.p.; single dose
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Result:Showed time-dependent covalent modification of ~70 kDa and ~110 kDa hepatic proteins, with signal intensity more prominent in benoxaprofen-treated livers compared to controls, and signals persisting through 24 h post-administration.
化学情報
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CAS 番号 51234-28-7
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性状 Solid
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分子量 301.72
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分子式 C16H12ClNO3
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Color White to light yellow
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SMILES
O=C(O)C(C)C1=CC=C(OC(C2=CC=C(Cl)C=C2)=N3)C3=C1
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別名
LRCL 3794
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
純度とドキュメンテーション
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データシート (275 KB)
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SDS (480 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Knights KM, et al. Benoxaprofen induced toxicity in isolated rat hepatocytes. Toxicology. 1986;40(3):327-339. [Content Brief]
[2]. Levine L, et al. Inhibition of the A-23187-stimulated leukotriene and prostaglandin biosynthesis of rat basophil leukemia (RBL-1) cells by nonsteroidal anti-inflammatory drugs, antioxidants, and calcium channel blockers. Biochem Pharmacol. 1983;32(20):3023-3026. [Content Brief]
[3]. Dong JQ, et al. Role of benoxaprofen and flunoxaprofen acyl glucuronides in covalent binding to rat plasma and liver proteins in vivo. Biochem Pharmacol. 2005;70(6):937-948. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Benoxaprofen 関連分類
HY-13568 関連分類
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