Oxazolone 是一种半抗原化剂,能够诱导急性或慢性大肠炎症,用于构建结肠炎模型。Oxazolone 引起的 Th1/Th2 依赖性结肠炎,伴随体重减轻和腹泻,可通过抗 IL-4 或抗 TNF-α 抗体或诱饵 IL-13R2α-Fc 蛋白减轻。


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| 描述 | Oxazolone acts as a haptenizing agent that triggers acute or chronic inflammation in the large intestine, making it suitable for developing colitis models. It leads to Th1/Th2-dependent colitis characterized by weight loss and diarrhea. The inflammation caused by oxazolone can be alleviated with neutralizing antibodies against IL-4 or TNF-α or with decoy IL-13R2-α-FC proteins[1]. |
| Concentration | Treated Time | Description | References | |
| Nrf2 (+/+) and Nrf2 (−/−) mouse embryonic fibroblasts (MEFs) | 10 µM | 24 hours | To evaluate the effect of oxazolone on transcriptional activation of Th2 cytokines, results showed that NRF2 suppresses oxazolone-induced production of Th2 cytokines. | Antioxidants (Basel). 2020 Sep 7;9(9):834 |
| HaCaT cells | 50 µM | 24 hours | To evaluate the effects of Oxazolone on oxidative stress and inflammatory responses in HaCaT cells. Results showed that Oxazolone significantly increased intracellular ROS levels and inflammatory cytokine expression, while D. dasycarpus and P. cicadae effectively reduced these effects. | Antioxidants (Basel). 2018 Jun 15;7(6):77 |
| Sheep red blood cells (SRBC) | 0.163 mg/ml | 30 minutes | To measure haemagglutinating antibody to oxazolone in mice, results showed that pooled sera from immunized mice had a haemagglutination titre of 27–29, while sera from unimmunized mice had no detectable antibody. | Immunology. 1972 Sep;23(3):289-98 |
| Administration | Dosage | Frequency | Description | References | ||
| BALB/c mice | Oxazolone-induced atopic dermatitis model | Topical application on ears | 0.1% oxazolone solution | Every 48 hours for 10 times | To evaluate the oxazolone-induced atopic dermatitis model and its therapeutic effects. Oxazolone-induced dermatitis showed ear swelling, skin inflammation, and elevated immunoglobulin levels. PFS treatment significantly alleviated these symptoms. | Mediators Inflamm. 2020 Oct 15;2020:4346367 |
| Balb/c mice | Oxazolone-induced atopic dermatitis model | Topical application | 0.2 mg/mouse | Ear thickness was measured every five days for 24 days | To evaluate the inhibitory effect of cardamonin on oxazolone-induced atopic dermatitis, results showed that cardamonin significantly suppressed oxazolone-induced inflammation and Th2 cytokine production. | Antioxidants (Basel). 2020 Sep 7;9(9):834 |
| BALB/c mice | Atopic dermatitis model | Topical application on the ear | 0.8% for sensitization, 0.4% for challenge | After 1 week of sensitization, every second day for a total of 5 times | To evaluate the effect of cesarean section and vaginal delivery on atopic dermatitis in mice. Results showed that CS-delivered mice and mice inoculated with human CS-GM had higher serum IgE concentrations, but the severity of dermatitis was similar among all groups. | Gut Microbes. 2023 Dec;15(2):2271151 |
| BALB/c mice | Oxazolone-induced AD-like skin inflammation model | Topical administration | 1% OXA | Once daily for 1 week | To evaluate the effect of A63 extract on OXA-induced AD-like skin inflammation. Results showed that A63 extract significantly reduced epidermal thickness and inflammatory cell infiltration, and downregulated the expression of AD gene markers. | Molecules. 2022 Apr 25;27(9):2751 |
| BALB/c mice | Oxazolone-induced AD-like lesion model | Topical application to ear surfaces | 1% Oxazolone | Once daily for 7 days, then every 2 days for 3 weeks | To evaluate Oxazolone-induced AD-like lesions. Oxazolone treatment increased ear thickness and epidermal thickness and increased mast cell infiltration. DCE significantly improved these symptoms. | Nutrients. 2022 Oct 27;14(21):4521 |
| Mice | Oxazolone colitis model | Intrarectal administration | 1.5% oxazolone | Single dose, assessed after 3 days | To evaluate the role of IL-33 and ST2 in oxazolone colitis. Results showed increased colitis severity, decreased goblet cells, and impaired epithelial barrier function in IL-33?/? and ST2?/? mice. | Inflamm Bowel Dis. 2015 Dec;21(12):2737-46 |
| Mice | Mouse lymph node model | Topical application | 10% | Single dose | To study the effects of antigenic stimulation on the expansion of T-cell-dependent areas in lymph nodes. Results showed rapid expansion of T-cell-dependent areas after Oxazolone stimulation, but the increase in HEV lagged behind the expansion of the T-cell area. | Immunology. 1990 Nov;71(3):423-7 |
| BALB/c mice | Oxazolone-induced intestinal colitis model | Intrarectal administration | 20 mg/kg | Once daily for six consecutive days | To investigate the effects of exogenous CRAMP on oxazolone-induced colitis, 20 mg/kg CRAMP significantly improved body weight regain, reduced colon weight/length ratio, and ameliorated colon tissue inflammation | Hum Vaccin Immunother. 2018 Jan 2;14(1):146-158 |
| Mice | Oxazolone-induced contact hypersensitivity model | Topical application | 25 μl (100 mg/mL) for sensitization, 10 μl (10 mg/mL) for challenge | Sensitization for two days, single challenge | To investigate the interaction of Breg cells, mast cells, and ILC2s in oxazolone-induced contact hypersensitivity, results showed that mast cells maintain Breg cell numbers via IL-5, and Breg cells suppress ILC2 activity via IL-10, thereby alleviating skin inflammation. | Sci Adv. 2019 Jul 17;5(7):eaav8152 |
| C57BL/6J mice | Contact hypersensitivity model | Topical application | 3% OX for sensitization, 1% OX for challenge | Single sensitization, single challenge after 5 days | To investigate basophil migration in the oxazolone-induced contact hypersensitivity model. Results showed a decrease in peripheral blood basophil numbers one day after challenge, but not after 2 days, reflecting supplementation from the bone marrow. | Front Immunol. 2022 Sep 29;13:1014924 |
| C57BL/6 mice | Oxazolone-induced colitis model | Catheter injection | 3% Oxa solution | Single injection | To study the Oxazolone-induced colitis model, which mimics the type 2 immune response in ulcerative colitis (UC) patients. Results showed that Oxazolone-induced colitis mice exhibited significant inflammatory responses. | Front Immunol. 2022 Jan 18;12:783806 |
| CBA mice | Contact sensitivity model | Skin application | 3% oxazolone | Single dose, tested after 7 days | To study contact sensitivity to oxazolone in mice, results showed that antibodies of IgM, IgG1, IgG2a, and IgG2b classes were detected in sera from immunized mice, while low-avidity antibodies were detected in sera from unimmunized mice. | Immunology. 1972 Sep;23(3):289-98 |
| BALB/c mice | Oxazolone-induced colitis model | Abdominal application and intrarectal administration | 3% oxazolone for abdominal sensitization, 1% oxazolone for intrarectal administration | Intrarectal administration 7 days after sensitization, experiment lasted for 3 days | To investigate the role of IL-4Rα signaling in specific cell types (e.g., intestinal epithelial cells, smooth muscle cells, and macrophages/neutrophils) in oxazolone colitis. Results showed that IL-4Rα signaling in these cell types plays a redundant role in acute oxazolone colitis. | Mediators Inflamm. 2020 Jan 17;2020:4361043 |
| CBA mice | Contact sensitization model | Topical application | 3% Oxazolone solution | Weekly | To investigate the effect of contact sensitization and boosting on the production of Oxazolone-specific cytophilic antibodies | Immunology. 1974 Oct;27(4):563-76 |
| Sprague Dawley rats | Oxazolone-induced ulcerative colitis model | Topical application on the back and anal injection | 30 mg/mL | One-time topical application on the back, followed by anal injection five days later | Evaluate the effect of Oxazolone-induced ulcerative colitis model, results showed Oxazolone successfully induced colitis symptoms, including colon shortening, splenomegaly, inflammatory cell infiltration, and tissue damage. | Molecules. 2019 Dec 24;25(1):76 |
| Hairless male ICR mice | Oxazolone-induced allergic contact dermatitis model | Topical application | 5% (initial sensitization) and 1% (subsequent challenges) | Initial sensitization once, followed by challenges every other day for 10 days | To assess the effects of Oxazolone on inflammatory responses and skin damage in mice. Results showed that Oxazolone significantly increased skin thickness and inflammatory cell infiltration, while D. dasycarpus and P. cicadae significantly alleviated these effects. | Antioxidants (Basel). 2018 Jun 15;7(6):77 |
| BALB/c mice | Oxazolone-induced atopic dermatitis-like skin lesions | Topical application | 5% OX for sensitization, 0.5% OX for challenge | Twice a week after sensitization for three weeks | To evaluate the severity of oxazolone-induced atopic dermatitis-like skin lesions, including increased ear thickness and weight, thickening of the epidermis and dermis, mast cell infiltration, and elevated serum IgE levels. Results showed that oxazolone successfully induced atopic dermatitis-like skin lesions. | Mar Drugs. 2022 Oct 26;20(11):669 |
| C57BL/6 mice | Oxazolone-induced contact dermatitis model | Topical application | 50 μl 2% OXA for sensitization, 25 μl 1% OXA for challenge | Sensitization once, challenge once, evaluated after 24 hours | To investigate the role of the LTB4–BLT1 axis in Oxazolone-induced contact dermatitis. Results showed that BLT1 deficiency or blockade of LTB4 and BLT1 by antagonists significantly reduced ear swelling and skin-infiltrating neutrophils and CD8+ T cells. | Immunology. 2015 Sep;146(1):50-8 |
| Mice | Intestinal-specific VDR knockout mice | Rectal administration | 5μl/g | Single dose, observed for 5 days | To investigate the protective effect of intestinal-specific VDR knockout on oxazolone-induced colitis, results showed that VDR knockout alleviated the severity of colitis | Cell Death Dis. 2020 Jun 15;11(6):461 |
| Wistar rats | Oxazolone-induced ulcerative colitis | Intracolonic administration | 7.5 mg/mL | Single dose | Induction of ulcerative colitis model to study the therapeutic effects of β-glucan and/or Celastrol | Redox Rep. 2022 Dec;27(1):60-69 |
| Wistar albino male rats | Oxazolone-induced ulcerative colitis model | Rectal administration | 7.5 mg/mL, 1.1 mL/rat | Single dose | Induction of ulcerative colitis model to study the moderating effects of β-glucan and/or aldose reductase inhibitor Fidarestat on the gut microbiome/mitochondrial axis. | Int J Mol Sci. 2023 Jan 31;24(3):2711 |
| SJL/J female mice | Oxazolone-induced colitis model | Intraperitoneal injection | 8, 2, or 0.5 mg/kg | Once every 2 days, for a total of five doses | To evaluate the efficacy of the bifunctional IL-4/IL-13 antagonist in the oxazolone-induced colitis model. Results showed that the antagonist reduced body weight loss, maintained colon length, minimized gains in colon weight, and reduced disease activity index. | Immunology. 2014 Nov;143(3):416-27 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.60mL 0.92mL 0.46mL |
23.02mL 4.60mL 2.30mL |
46.04mL 9.21mL 4.60mL |
|
| CAS号 | 15646-46-5 |
| 分子式 | C12H11NO3 |
| 分子量 | 217.22 |
| SMILES Code | O=C(OC(C1=CC=CC=C1)=N2)C2=COCC |
| MDL No. | MFCD00003204 |
| 别名 | |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(483.38 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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