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MK-0812

    98%

MK-0812

源葉(MedMol)
S86007
624733-88-6
C24H34F3N3O3
469.55
1,5-酐-2,3-雙脫氧-3-[[(1R,3S)-3-[[7,8-二氫-3-(三氟甲基)-1,6-萘啶-6(5H)-基]羰基]-3-(1-甲基乙基)環(huán)己基]氨基]-4-O-甲基-D-赤式-戊糖醇
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)買數(shù)量
源葉(MedMol) S86007-2mg 98% ¥1300.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S86007-5mg 98% ¥2300.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S86007-10mg 98% ¥3800.00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

MK-0812 is an effective and specific CCR2 antagonist.
產(chǎn)品描述: MK-0812 is an effective and specific CCR2 antagonist.
靶點(diǎn): CCR
體內(nèi)研究: MK0812 (30 mg/kg, p.o.) reduces the frequency of Ly6G-Ly6Chi monocytes in the peripheral blood, while no impact on circulating Ly6G+Ly6C+ neutrophil frequency is observed. In addition, MK0812 treatment causes a dose-dependent reduction in circulating Ly6Chi monocytes and a corresponding elevation in the CCR2 ligand CCL2
細(xì)胞實(shí)驗(yàn): Female BALB/c mice are used between 8 and 10 weeks of age. MK0812 are administered in a 0.4% MC solution by 30 mg/kg oral gavage (p.o.). Two hours later, the frequency of CD11b+Ly6G-Ly6Chi monocytes and CD11b+Ly6G+Ly6C+ neutrophils is determined by flow cytometry
參考文獻(xiàn): 1. Wisniewski T, et al. Assessment of chemokine receptor function on monocytes in whole blood: In vitro and ex vivo evaluations of a CCR2 antagonist.J Immunol Methods. 2010 Jan 31;352(1-2):101-10. 2. Min SH, et al. Pharmacological targeting reveals distinct roles for CXCR2/CXCR1 and CCR2 in a mouse model of arthritis.Biochem Biophys Res Commun. 2010 Jan 1;391(1):1080-6.
溶解性: Soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.13 ml 10.648 ml 21.297 ml
5 mM 0.426 ml 2.13 ml 4.259 ml
10 mM 0.213 ml 1.065 ml 2.13 ml
50 mM 0.043 ml 0.213 ml 0.426 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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