Diflorasone 是一种皮质类固醇激素受体激动剂,具备抗炎和免疫抑制的特性。它能够通过细胞膜扩散进入细胞内部,并与细胞质中的糖皮质激素受体(GR)结合。Diflorasone 可用于湿疹、牛皮癣等皮肤疾病的科学研究。


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| 描述 | Diflorasone act as a corticosteroid hormone receptor agonist with anti-inflammatory and immunosuppressive properties. Diflorasone enters the cell by diffusion across the cell membrane and binds to the glucocorticoid receptor (GR) in the cytoplasm[1]. 0.05% diflorasone diacetate cream was as effective as 0.05% fluocinonide cream in the therapy of lesions of psoriasis or atopic/neurodermatitis[2]. Diflorasone inhibits RANTES and thymus and activation regulated chemokine (TARC) in a dinitrochlorobenzene-induced mouse model of allergic contact dermatitis[3]. It also inhibits proliferation of human keratinocytes in vitro and reduces epidermal thickening in a mouse model of psoriasis induced by imiquimod[4]. |
| Concentration | Treated Time | Description | References | |
| human peripheral blood T cells | 1 µM | 6 h | To evaluate the effect of Diflorasone on cytokine production, results showed that Diflorasone significantly inhibited the release of IL-2 and other cytokines. | Cell Commun Signal. 2025 Jun 4;23(1):268 |
| human peripheral blood T cells | 1 µM | 2 h | To evaluate the effect of Diflorasone on TCR signaling, results showed that Diflorasone did not affect early TCR signaling. | Cell Commun Signal. 2025 Jun 4;23(1):268 |
| human peripheral blood T cells | 1 µM | 2 h | To evaluate the effect of Diflorasone on T cell proliferation, results showed that Diflorasone significantly inhibited T cell proliferation. | Cell Commun Signal. 2025 Jun 4;23(1):268 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.44mL 0.49mL 0.24mL |
12.18mL 2.44mL 1.22mL |
24.36mL 4.87mL 2.44mL |
|
| CAS号 | 2557-49-5 |
| 分子式 | C22H28F2O5 |
| 分子量 | 410.45 |
| SMILES Code | O=C1C=C[C@]2(C)C3(F)[C@@H](O)C[C@]4(C)[C@](C(CO)=O)(O)[C@@H](C)C[C@@]4([H])[C@]3([H])C[C@H](F)C2=C1 |
| MDL No. | MFCD00200358 |
| 别名 | 地弗拉松 |
| 运输 | 蓝冰 |
| InChI Key | WXURHACBFYSXBI-XHIJKXOTSA-N |
| Pubchem ID | 71415 |
| 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: 125 mg/mL(304.54 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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