CAS NO: | 848057-98-7 |
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 | SPHINX is a selectiveSRPK1inhibitor with anIC50value of 0.58 μM. SPHINX effectively reduces Choroidal Neovascularization (CNV) in vivo. SPHINX can be used for the research of (age-related macular degenaration) AMD[1]. | ||||||||||||||||
IC50& Target | IC50: 0.58 μM (SRPK1)[1] | ||||||||||||||||
体外研究 (In Vitro) | SPHINX (10 μM; 2 h) affects EGF-induced phosphorylation of SRSF1 and SRSF2[1].SPHINX (5 μM; 24 h) reduces the expression of VEGF165 relative to GAPDH control either in primary RPE and ARPE-19 cell lines[1]. Western Blot Analysis[1]
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体内研究 (In Vivo) | SPHINX (10 ng; i.o. on laser photocoagulation day 0 and day 7) affects neovascular growth in vivo[1].SPHINX (25 ng; i.o. on laser photocoagulation day 0 and day 7) affects the CNV area in CNV rats[1].
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Clinical Trial | |||||||||||||||||
分子量 | 354.32 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H17F3N2O3 | ||||||||||||||||
CAS 号 | 848057-98-7 | ||||||||||||||||
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 : 50 mg/mL(141.12 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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