CAS NO: | 869296-13-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | T-26c is highly potent and selectivematrix metalloproteinase-13 (MMP-13)inhibitor with anIC50of 6.75 pM and more than 2600-fold selectivity over the other related metalloenzymes[1]. | ||||||||||||||||
IC50& Target | IC50: 6.75 pM (MMP-13)[1] | ||||||||||||||||
体外研究 (In Vitro) | T-26c significantly inhibits the breakdown of collagen (87.4% inhibition at 0.1 μM) in IL-1β and oncostatin M stimulated cartilage[1]. | ||||||||||||||||
体内研究 (In Vivo) | T-26c is well absorbed in all species at the oral dose of 10–20 mg/kg. Oral administration of the disodium salt formulations of T-26c to guinea pigs results in significant increases in AUC (8357 ng h/mL) and Cmax(1445 ng/ mL) compared with those of the free acid T-26c (AUC = 6478 ng h/ mL and Cmax= 911 ng/mL)[1]. | ||||||||||||||||
分子量 | 479.51 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H21N3O6S | ||||||||||||||||
CAS 号 | 869296-13-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 15.62 mg/mL(32.57 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro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,建议您现用现配,当天使用;
以下溶剂前显示的百
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