CAS NO: | 1564286-55-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | CWHM-12 is a potent inhibitor ofαV integrinswithIC50s of 0.2, 0.8, 1.5, and 1.8 nM forαvβ8,αvβ3,αvβ6, andαvβ1. | ||||||||||||||||
IC50& Target | IC50: 0.2 nM (αvβ8), 0.8 nM (αvβ3), 1.5 nM (αvβ6), 1.8 nM (αvβ1), 61 nM (αvβ5)[1] | ||||||||||||||||
体外研究 (In Vitro) | CWHM-12 (CWHM 12) also less potently inhibits αvβ5 (IC50=61 nM) and αIIbβ3/α2β1/α10β1 (IC50>5000 nM). CWHM-12 demonstrates high potency against all of the five possible β subunit binding partners (αvβ1, αvβ3, αvβ5, αvβ6 and αvβ8) in in vitro ligand-binding assays, with somewhat less potency against αvβ5 than against the other αv integrins[1]. | ||||||||||||||||
体内研究 (In Vivo) | Mice are treated with CCl4for 3 weeks to establish fibrotic disease and then treated with CWHM-12 (CWHM 12) or vehicle for the final 3 weeks of CCl4. CWHM-12 significantly reduces liver fibrosis even after fibrotic disease have been established. Digital image quantitation demonstrates significantly reduced p-SMAD3 signaling in the livers of CWHM-12 treated mice compare to controls, demonstrating that the protection from CCl4-induced hepatic fibrosis observed in CWHM-12 treated mice is due at least in part to a reduction in TGF-β activation by αv integrins. Besides, administration of CWHM-12 significantly inhibited progression of pulmonary fibrosis[1]. | ||||||||||||||||
分子量 | 590.47 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H32BrN5O6 | ||||||||||||||||
CAS 号 | 1564286-55-0 | ||||||||||||||||
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 : 100 mg/mL(169.36 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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