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SLV-2436

    98%

SEL201-88; SEL-201

源葉(MedMol)
S88568
2095704-43-9
C19H15ClN4O
350.8
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 購(gòu)買(mǎi)數(shù)量
源葉(MedMol) S88568-1mg 98% ¥595.00元 5 - - -
源葉(MedMol) S88568-5mg 98% ¥1460.00元 7 - - -
源葉(MedMol) S88568-10mg 98% ¥2350.00元 6 - - -
源葉(MedMol) S88568-25mg 98% ¥3900.00元 6 - - -
源葉(MedMol) S88568-50mg 98% ¥5700.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S88568-100mg 98% ¥7800.00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(shū)(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

SLV-2436 is a highly potent and ATP-competitive inhibitor of MNK1 and MNK2 with IC50s of 10.8 ?nM and 5.4 nM, respectively.
產(chǎn)品描述: SLV-2436 is a highly potent and ATP-competitive inhibitor of MNK1 and MNK2 with IC50s of 10.8 ?nM and 5.4 nM, respectively.
靶點(diǎn): MNK2:5.4 nM (IC50);MNK1:10.8 nM (IC50);MNK
體外研究: To confirm the kinome selectivity of SLV-2436 (SEL201), the broad KINOMEscan competitive binding assay is performed at 1 μM, which includes 450 distinct kinases. The observed binding profile for SLV-2436 is significantly concentrated in the CAMK family of kinases that comprises MNK1 and MNK2. SLV-2436-treated KIT-mutant melanoma cells have lower oncogenicity and reduced metastatic ability
體內(nèi)研究: To investigate the pharmacodynamic properties of SLV-2436 (SEL201), 5 consecutive oral doses of 10, 25, and 50 mg/kg are administered to mice every 12 hours (twice-daily schedule). At the 10 mg/kg twice-daily dosage, 4 hours after the fifth administration, a low plasma concentration of 125 ng/mL SLV-2436 is determined. However, dosing at 25 and 50 mg/kg twice daily, equivalent to 50 and 100 mg/kg/d of SLV-2436, yields substantially increased dose-dependent plasma exposure, reaching an average level of 1,299 ng/mL and 2,075 ng/mL, respectively. At the 24-hour time point, SLV-2436 is still detectable in the plasma, with dose-dependent concentrations of 9, 73, and 124 ng/mL in the 10, 25, and 50 mg/kg twice-daily treatment groups. Oral (p.o.) administration of SLV-2436 at the dosage of 50 mg/kg twice daily, that is, 100 mg/kg/d, for 37 days is well tolerated in mice
參考文獻(xiàn): 1. Zhan Y, et al. MNK1/2 inhibition limits oncogenicity and metastasis of KIT-mutant melanoma. J Clin Invest. 2017 Nov 1;127(11):4179-4192.
溶解性: Soluble  in  DMSO
保存條件: -20°C
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.851 ml 14.253 ml 28.506 ml
5 mM 0.57 ml 2.851 ml 5.701 ml
10 mM 0.285 ml 1.425 ml 2.851 ml
50 mM 0.057 ml 0.285 ml 0.57 ml
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參考文獻(xiàn)

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