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Epetraborole (hydrochloride)

    99%

Epetraborole (hydrochloride)

源葉(MedMol)
S82514
1234563-16-6
C11H17BClNO4
273.521
(S)-3-aminomethyl-7-(3-hydroxy-propoxy)-3H-benzo[c][1,2]oxaborol-1-ol hydrochloride; (3S)-3-(aminomethyl)-7-[(3-hydroxypropyl)oxy]-2,1-benzoxaborol-1(3H)-ol hydrochloride;
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S82514-1mg 99% ¥650.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S82514-2mg 99% ¥950.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S82514-5mg 99% ¥1530.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S82514-10mg 99% ¥2300.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S82514-50mg 99% ¥9000.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S82514-100mg 99% ¥15000.00元 預(yù)計(jì)交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Epetraborole (GSK2251052) hydrochloride is a novel leucyl-tRNA synthetase (LeuRS) inhibitor (IC50=0.31 μM), thereby inhibiting protein synthesis. Epetraborole hydrochloride can be used in multidrug-resistant gram-negative pathogens infection research
產(chǎn)品描述: Epetraborole (GSK2251052) hydrochloride is a novel leucyl-tRNA synthetase (LeuRS) inhibitor (IC50=0.31 μM), thereby inhibiting protein synthesis. Epetraborole hydrochloride can be used in multidrug-resistant gram-negative pathogens infection research
靶點(diǎn): IC50: 0.31 μM (LeuRS);Antibacterial
體外研究: Epetraborole (0-32 μg/mL) shows anti-bacterial activity against key gram-negative aerobic and anaerobic pathogens and gram-positive anaerobes. Cell Viability Assay Cell Line: Anaerobes isolates Concentration: 0-32 μg/mL Incubation Time: Result: Showed MIC50/MIC90 for all anaerobes isolates tested of 2 and 4 μg/mL, respectively.
參考文獻(xiàn): 1. Goldstein EJ, et al. Comparative in vitro activities of GSK2251052, a novel boron-containing leucyl-tRNA synthetase inhibitor, against 916 anaerobic organisms. Antimicrob Agents Chemother. 2013 May;57(5):2401-4. 2. O'Dwyer K, et al. Bacterial resistance to leucyl-tRNA synthetase inhibitor GSK2251052 develops during treatment of complicated urinary tract infections. Antimicrob Agents Chemother. 2015 Jan;59(1):289-98. 3. Sutcliffe JA. Antibiotics in development targeting protein synthesis. Ann N Y Acad Sci. 2011 Dec;1241:122-52.
溶解性: Soluble  in  DMSO、H2O
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.656 ml 18.28 ml 36.56 ml
5 mM 0.731 ml 3.656 ml 7.312 ml
10 mM 0.366 ml 1.828 ml 3.656 ml
50 mM 0.073 ml 0.366 ml 0.731 ml
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參考文獻(xiàn)

質(zhì)檢證書(COA)

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摩爾濃度計(jì)算器

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