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SPHINX31

    
98%

SPHINX31

源葉(MedMol)
S29704 一鍵復制產品信息
1818389-84-2
C27H24F3N5O2
507.51
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S29704-5mg 98% ¥235.00 9 - - -
S29704-25mg 98% ¥790.00 8 - - -
S29704-100mg 98% ¥1955.00 貨期:2-3天 - - -
S29704-250mg 98% ¥3800.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

SPHINX31 is a potent and selective SRPK1 inhibitor, with an IC50 of 5.9 nM. SPHINX31 inhibits phosphorylation of serine/arginine-rich splicing factor 1 (SRSF1). SPHINX31 also decreases the mRNA expression of pro-angiogenic VEGF-A165a isoform. SPHINX31 can be used to research neovascular eye disease

產品描述: SPHINX31 is a potent and selective SRPK1 inhibitor, with an IC50 of 5.9 nM. SPHINX31 inhibits phosphorylation of serine/arginine-rich splicing factor 1 (SRSF1). SPHINX31 also decreases the mRNA expression of pro-angiogenic VEGF-A165a isoform. SPHINX31 can be used to research neovascular eye disease
靶點: IC50: 5.9 nM (SRPK1) VEGF-A165a[2;Serine/threoninkinase
體內研究: SPHINX31 (200 μg/mL; twice daily topical eye drops) protects the retinal endothelial permeability barrier from diabetes-associated loss of integrity
參考文獻: 1. Batson J, et al. Development of Potent, Selective SRPK1 Inhibitors as Potential Topical Therapeutics for Neovascular Eye Disease. ACS Chem Biol. 2017 Mar 17;12(3):825-832. 2. Supradit K, et al. Inhibition of serine/arginine-rich protein kinase-1 (SRPK1) prevents cholangiocarcinoma cells induced angiogenesis. Toxicol In Vitro. 2022 Aug;82:105385. 3. C. Allen, et al. The SRPK1 inhibitor SPHINX31 prevents increased retinal permeability in a rodent model of diabetes. Acta Ophthalmologica. Volume 95, Issue S259.
溶解性: DMSO  :  17.33  mg/mL  (34.15  mM;  Need  ultrasonic)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.97 ml 9.852 ml 19.704 ml
5 mM 0.394 ml 1.97 ml 3.941 ml
10 mM 0.197 ml 0.985 ml 1.97 ml
50 mM 0.039 ml 0.197 ml 0.394 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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請輸入貨號和一個與之匹配的批號。
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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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