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Merimepodib 98%

Merimepodib

MedMol
S84258
198821-22-6
C23H24N4O6
452.4599
Merimepodib (USAN/INN); VX-497; Merimebodib; Tyverb/Tykerb; MMPD; Merimepodib;
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
MedMol S84258-2mg 98% ¥408.00元 5 - - -
MedMol S84258-5mg 98% ¥680.00元 6 - - -
MedMol S84258-10mg 98% ¥1224.00元 6 - - -
MedMol S84258-25mg 98% ¥2312.00元 6 - - -
源葉(MedMol) S84258-50mg 98% ¥3900.00元 預(yù)計交期:2-3天 - - -
源葉(MedMol) S84258-100mg 98% ¥5700.00元 預(yù)計交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Merimepodib (VX-497) is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.
產(chǎn)品描述: Merimepodib (VX-497) is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.
靶點: HBV;HCV;Dehydrogenase;?Antiviral;?HCVProtease;?HBV
體外研究: VX-497 has antiproliferative effect on lymphoid and keratinocyte cells. The antiproliferative effect of VX-497 in cells is reversed within 48 h of its removal. VX-497 has intermediate antiviral activity against a second group of viruses, which includes HSV-1, parainfluenza-3 virus, BVDV, VEEV, and dengue virus, with IC50s ranging from 6 to 19 μM. VX-497 is 100-fold more potent, with an IC50 of 380 nM and a corresponding CC50 of 5.2 μM, for a therapeutic index of 14. The antiviral activity of VX-497 in HepG2.2.2.15 cells is reversed threefold by the addition of guanosine
體內(nèi)研究: Oral administration of VX-497 inhibits the primary IgM antibody response in a dose-dependent manner, with an ED50 value of appr 30-35 mg/kg in mice. Single daily dosing of VX-497 is observed to be as effective as twice-daily dosing in this model of immune activation. GVHD developed in the vehicle-treated allografted F1 mice and treatment with VX-497 improved all manifestations of the disease significantly. The 2.9-fold increase in spleen weight in allografted animals is reduced to a 1.6-fold increase in the VX-497-treated mice. Serum IFN-gamma levels are increased 54-fold in the vehicle group while there is a 7.4-fold increase in VX-497-treated animals
參考文獻(xiàn): 1. Jain J, et al. VX-497: a novel, selective IMPDH inhibitor and immunosuppressive agent. J Pharm Sci. 2001 May;90(5):625-37. 2. Markland W, et al. Broad-spectrum antiviral activity of the IMP dehydrogenase inhibitor VX-497: a comparison with ribavirin and demonstration of antiviral additivity with alpha interferon. Antimicrob Agents Chemother. 2000 Apr;44(4):859-66. 3. Decker CJ, et al. The novel IMPDH inhibitor VX-497 prolongs skin graft survival and improves graft versus host disease in mice. Drugs Exp Clin Res. 2001;27(3):89-95.
溶解性: Soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.21 ml 11.051 ml 22.101 ml
5 mM 0.442 ml 2.21 ml 4.42 ml
10 mM 0.221 ml 1.105 ml 2.21 ml
50 mM 0.044 ml 0.221 ml 0.442 ml
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