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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
188817-13-2
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥660.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥566.0 |
| 规格: | 10 mg | 产品价格: | ¥1076.0 |
| 规格: | 25 mg | 产品价格: | ¥2400.0 |
| 规格: | 50 mg | 产品价格: | ¥3600.0 |
| 规格: | 100 mg | 产品价格: | ¥5300.0 |
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SC-560
CAS No. : 188817-13-2
MCE 国际站:SC-560
产品活性:SC-560是有效,选择性的 COX-1 抑制剂,IC50 值为9 nM。
作用靶点:COX
In Vitro: Preincubation of COX-1 with SC-560 inhibits the conversion of arachidonic acid to PGE2 in a concentration-dependent manner. The IC50 of SC-560 for COX-2 is 6.3 μM, nearly 1,000-fold higher than with COX-1. SC-560 shows a dose and time dependent inhibitory effect on HCC cell growth. SC-560 also inhibits colony formation in soft agar and induces apoptosis in HCC cells in a dose-dependent manner. Moreover, SC-560 decreases the levels of the anti-apoptotic proteins survivin and XIAP and activates caspase 3 and 7 in a dose and time dependent fashion.
In Vivo: Oral dosing with either 10 or 30 mg/kg SC-560 1 hour before assay completely inhibits ionophore-stimulated TxB2production, indicating that SC-560 is orally bioavailable and inhibits COX-1 in vivo. SC-560 extensively distributes into rat tissues, and has a CL approaching hepatic plasma flow. The drug displays low less than 15% and formulation dependent bioavailability after oral administration and demonstrates kidney toxicity.
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文献和实验2,表 1) 证实了其安全性和有效性 [1, 2]。 AAV 在骨科研究中的应用案例 应用案例 1:骨关节炎的 AAV 基因治疗[3] 研究背景:骨关节炎(OA)是一种全球性的重大健康问题,目前尚无疾病修饰疗法。白细胞介素-1(IL-1)是与 OA 病 理生理学相关的关键细胞因子,可通过 IL-1 受体拮抗剂(IL-1Ra)抑制。研究团队开发了一种自互补型重组 AAV 载体(sc-rAAV2.5IL-1Ra),用于将 IL-1Ra 基因递送至膝关节。 研究方法: 试验设计:这是一项开放标签、单
色素沉着是生物发光成像中的一个重要变量,在纵向研究的实验设计和实施中应该考虑到该变量,特别是当需要对弱信号变化或动物之间的差异研究时。由于黑色素的吸收系数随波长的增加而降低,黑色素对较短波长(即在可见光谱中)的光的吸收作用比在近红外波长的光对更强。荧光成像可以使用近红外染料,它们具有较长波长的发射光谱,使它们对黑色素吸收的敏感性较低。然而,生物发光成像并不具备这个优势。萤火虫荧光素酶的发射峰约为 560 nm,使生物发光信号从与其相互作用的组织产生显著的散射和吸收效应,进而改变了从动物身上产生的信号的强度
, Travis WD, Emmert-Buck MR. Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung. Hum Mol Genet 6(13):2285-90, 1997. Emmert-Buck, MR, Lubensky, IA, Dong, Q, Chandrasekharappa, C, Guru, SC, Manickam, P, Keseter, M, Olufemi, S-E
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